Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Job Title/Role : Sr. Support Manager, Interactive Response Technology Department Name/Functional Area : Global Clinical Supply Chain > Clinical Supply Chain Technologies > IRT Location : Office based . Position Summary This position supports multiple IRT studies (system development, study management, change management, audits and data provisioning). Supports UAT Services organization as required. Identifies areas of process improvement and participates or leads these initiatives. Duties/Responsibilities Lead successful maintenance support and projects to ensure execution and on time delivery of Interactive Response Technology (IRT) changes, data and support integrations with other clinical systems (e.g., Depots, Central Lab, and EDC), such that the resultant IRTs are fit-for-purpose as defined by protocol and study operational parameters with special emphasis on adherence to BMS standards and quality principles. Works independently and assume support role responsibilities on assigned projects. Collaborate with the IRT Team where necessary to ensure BMS standards and/or for requests by study teams that are not within these standards or best practice are addressed. Bring issues of concern or system failure to the immediate attention of the IRT Leadership Team. During IRT maintenance act as the primary contact for assigned studies for the cross-functional study team and vendor. Additionally, provide timely response to all randomization/IRT issues (including data integrations and delivery) that arise during IRT lifecycle and ensure they are resolved. Maintain vendor performance quality events in ADI log. Act as off hours audit/inspection support contact as needed to support rest of world. Responsible for generation and oversight of patient and container randomization schedules, ensuring parameters reflect the protocol and drug supply requirements. Distribute patient randomization and container schedules as appropriate to Clinical Supply P&L and IRT vendors. Manage special project implementation by identifying project needs, tracking, implementation, and reporting to a central project team. Bring issues of concern or system failure to the immediate attention of the IRT Leadership Team. Support IRT improvement initiatives and manages improvement projects that impact daily operations to improve efficiency. Support key department and enterprise level initiatives as part of the IRT representative. Ensure on time delivery of maintenance support and may be involved in user acceptance testing of IRT systems per BMS SOPs and procedures, write or review User Acceptance Test Plan and causes to ensure thorough testing of high -risked areas and new functionality documented in the user requirements. Ensure systems and associated documentation are compliant with all Regulatory requirements, including cGMP, 21 CFR Part 11, ICH E6 (R2) as well as in accordance BMS SOPs and processes. Ensure effective system access and functionality across all countries and all user locations. Complete all assigned training by due date Support unblinding activities as needed. Ensure on time development of IRT data transfers with vendors and/or third-party vendors. Ensure eTMF compliance at the study level in accordance with group and BMS guidance. Engage and support study and CSMT project teams as deemed necessary. Ensure delivery of data to BMS departments and third-party vendors consistent with BMS SOPs and forms. Additional tasks within scope of expertise and experience as assigned by the supervisor in pursuit of BMS goals. Reporting Relationship This position reports to the Associate Director, Interactive Response Technology (IRT). Qualifications Minimum bachelor s degree Minimum of 3 to 5 years work experience preferably in a health science or related IRT industry (pharmaceutical, hospital-based, laboratory, etc.) Demonstrated analytical skills and a working knowledge of Microsoft Office including SharePoint. Clinical Research experience Working knowledge of IRT Working knowledge of Clinical Trial Management Systems Working knowledge of clinical supplies Able to think outside of the box, have excellent communication and analytical skills to successfully deliver optimal IRT solutions across a diverse and dynamic portfolio. Understand the nature of clinical data and concepts of IRT study design and configuration, resupply settings, blinding, privacy protection, and data quality/integrity standards. Exposure to working in a GMP / GCP environment and with regulatory audit teams. Possess excellent English language written and verbal communication, interpersonal, collaboration and business partnership capabilities required Comfortable working with a global team, partners and customers in a change agile environment MS Project, MS Visio, or any other requirements visualization and analysis tools) With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Recruiter to add With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Role Summary Identification of potential customers, potential mapping of accounts and customers, promoting awareness about therapy area & promoting products as per company's objectives. Meeting doctors, pharmacists, purchase managers and hospital authorities to ensure smooth execution of marketing strategies and achievement of Organization's sales objectives for the assigned territory. HCP engagement in scientific activities Timely submission of sales data and various other related reports. Key responsibilities: Driving sales in the assigned territory as per organization's objectives. Potential mapping of doctors and institutions. Identify opportunities at marketplace, develop and maintain good relations with customers, hospital pharmacies, hospital authorities, distributors etc. Organize scientific meetings to enhance company's image, awareness about therapy area, products. Effective record keeping, maintain the data and timely submission of the data. Active participation in cycle meetings/ NSM to ensure sales skills, in-clinic effectiveness, product knowledge and competitor's knowledge is maintained. Manage the process of hospital formulary inclusion to allow usage of product in that hospital. Ensure BMS values and ethics are followed while conducting business. Qualifications: Pharmacy graduate or Science graduate, MBA preferred. Languages: English & Hindi. Local language as per geography. Experience and Knowledge : Pharma sales experience of at least 10 years. Knowledge of local market is an advantage. Cardiology Experience is preferred. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Responsibilities BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Show more Show less

Position Summary: As the Manager, Global Product Quality Complaints Device & Digital, you have expertise and experience in digital tools for optimal PQC processing and have expert knowledge in the management of complaints related to device/combination products. Reporting to the Senior Manager, Global Product Quality Complaints, HYD Lead, you will act as the Subject Matter Expert (SME) for device/combination products complaints, supporting continuous improvement initiatives, risk management, and mitigation strategies. You will also be responsible for delivering digital and automation solutions in line with BMS's digital strategy, ensuring their compliance with internal and global regulatory requirements. Your role includes designing, operating, and maintaining automation/RPA solutions and collaborating with stakeholders to resolve BOT operation issues, thereby minimizing interruptions to PQC processing. Additionally, you will partner with various teams to ensure effective data exchanges and support for adverse event investigations, identify critical quality issues, and develop corrective actions. You will also provide SME support for PQC trending activities and maintain technical expertise in business applications such as Spotfire. Key Responsibilities: Responsible to maintain a high level of knowledge & understanding of Pharmaceutical/Biologic Quality Assurance, Device Quality Assurance, cGood Manufacturing Practices as applicable in global GMP regulations (including FDA, EMA, MHRA, PMDA, ENVISA, TGA). Responsible to act as the Subject Matter Expert (SME) for processing of complaints related to devices and combination products. Responsible to engage and support Device Quality organization in continuous improvement of device complaint handling and data management. Responsible to support the risk management and mitigation related to device complaint management. Responsible for delivery of digital and automation solutions in line with the BMS digital strategy for PQC optimization. Ensure quality & compliance of digital solutions and automations with internal and global regulatory requirements, including evolving regulatory landscape. Accountable for the optimum design, operation and maintenance of automation/BOT solutions for PQC related processes. Responsible to work effectively and collaboratively with stakeholders business partners to escalate and resolve BOT operation issues, in order to minimise interruption to PQC processing and to maintain budget adherance. Provide ongoing management for PQCs ensuring compliance to global framework of GMP policies and BMS procedures Partner with WWPS to ensure effective exchanges through integrated systems and investigation for Adverse Events with PQC MedDRA codes Identify critical quality issues and assist in the investigation and implementation of corrective actions. Provide SME support for PQC trending activities using business applications such as Spotfire (PQC-MVT) and maintain technical expertise with regards to its build and operations Develop trusting, open and collaborative partnerships while ensuring stakeholders (affiliates, sites, functions) have clear understanding of PQC processes from intake to closure Oversee and improve reconciliation processes from intake sources (Medical Customer Engagement and WWPS) Provide SME support, liaise with ancillary groups for Device/Combination products ensuring robust processes and controls for Medical Device Reporting (MDR) and Device Malfunction assessments Lead quality risk management activities for complaint handling and promote the understanding of risk management for product quality complaints and surveillance activities and participate in project teams as needed. Manage all aspects of quality systems, such as documentation, trainings, change controls, quality agreements and computer system validations as necessary for complaint handling. Partner with global metrics team and PQC/PS support analytics teams to establish and generate complaint metrics and Key Performance Indicators (KPIs) and facilitate improvements for end-to-end complaint process. Conduct self-inspections on a periodic basis and provide support during audits and inspections Support Community of Practice forums with collection of topics, content preparation and presentation. Support PQC related audits and inspections as necessary As required by the Senior Manager HYD PQC Lead: Act as a delegate for Global Product Quality Triage support the management of the Global Product Quality Complaint (PQC) handling process from receipt to closure according to applicable timeframes and in compliance with BMS procedures and regulatory requirements Act as a delegate for the Manager, Global Product Quality Complaints Surveillance, completing PQC data assessments, highlighting trends, signals and risks and business critical information related to Product Quality Complaint data to Quality leadership in a timely fashion. Data & trend assessments will be communicated with stakeholders in a manner commensurate with risk and enabling appropriate action taking to protect BMS and our patients. Act as delegate for PQC Systems lead, ensuring optimal performance of system interfaces impacting PQC processing. Qualifications & Experience: Degree/Certification/Licensure Bachelor’s degree or higher in Life Sciences (Chemistry, Biology etc) or Health Sciences (Nursing, Pharmacy etc) or related discipline eg Engineering, Pharmaceutical Manufacturing etc. Advanced degree preferred. Qualification or proven experience in data analytics, automation or similar highly advantageous. Required Competencies: Fluent in English, with proven professional working proficiency in English for reading, writing and speaking Excellent communication with management, peers, and other functional areas Excellent ability to analyse processes, data and trends, and to translate into effective messaging to stakeholders and leaders supporting effective decision-making Proven ability to understand complex processes/problems and propose alternate solutions/automated solutions/process enhancements/efficiencies Experience in management of PQCs related to globally distributed pharma/BIO and device/combination products Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders Demonstrated Enterprise mindset to be able to think and act across functions and divisions Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives Highly organized, detail oriented, efficient operator in a fast-paced environment Excellent teamwork, interpersonal, and communication skills, with the ability to communicate and collaborate with employees and management at all levels and through various formats Demonstrated strategic thinking capability and ability to balance conflicting priorities Ability to provide innovative ideas or alternatives that create value including seeking new information and external insights without compromising compliance Ability to clearly articulate digital needs to functional partners Experience – Responsibility and minimum number of years: A minimum of 5 years of experience in a Quality role where data analytics and/or process automation was a key component in the pharmaceutical/ biotech/ device industry Strong working knowledge/experience with systems such as QMS, SAP/ERP, Veeva, automations Prior experience in the management of Product Quality Complaints for Pharma/BIO/device/clinical products is an advantage Experience with device/combination products Experience with understanding how to respond to trend signals within the context of quality surveillance Strong problem solving skills are required Strong program and project management skills Ability to manage multiple, simultaneous projects Thorough understanding of Quality Risk Management Mastery of relevant Quality compliance processes and regulations Show more Show less

Position Summary: This is a global role which supports the Patient Safety (PS) Mission and Vision through understanding the impact of daily work on all stakeholders of Safety Management Plans (SAE MP’s) and Pharmacovigilance Agreements (PVA’s).This role provides oversight of quality and process optimization working with multiple global stakeholders across PS and external functions to ensure business critical support to the management of and reporting associated with SAE MPs and PVAs. Major responsibilities will be the drafting, review, negotiation, execution and maintenance of SAE MPs and PVAs as assigned. Duties Responsibilities: Demonstrate strong teamwork skills to ensure accurate production of SAE MPs and PVAs including the processes, procedures, and best practices are consistent across PS and that regulatory requirements are met in a timely manner and with high quality Periodically review and update SAE MPs and PVAs per internal process Builds and maintains strong relationships with other BMS functional areas to complete and facilitate implementation of SAE MPs and PVAs Identifies ways to improve productivity and quality standards for SAE MP and PVA-related deliverables and actively participates in efforts to remedy non compliance situations Review and evaluate integrity of CRO SAE management processes for inspection readiness. Apply knowledge of specific work practices, Standard Operating Procedures (SOP), and regulations to maintain oversight of SAE MPs and PVAs and ensure successful execution of task Engage and develop working relationships with Preferred CROs and Business Partners to ensure alignment with BMS processes. Maintain a customer service focus with internal and external colleagues. Take personal initiative by proactively identifying innovative ways to accomplish tasks and drive toward process efficiencies. Utilize effective organizational skills to prioritize deliverables to accomplish work in established timeframes. Contribute to continuous quality improvement process through projects and other related departmental initiatives. Develop expertise in associated applications and web systems (e-TMF, Veeva Vault, PVA and SAE MP Management system. Show more Show less

Position Summary: This individual contributor role is responsible for managing in-house and outsourced studies while ensuring adherence to BMS outsourcing strategies within specific therapeutic areas. The role supports clinical trial vendor partnerships across select or multiple service categories of clinical trial activities in R&D. Key Responsibilities: Drive outsourcing activities by interfacing with operational teams, support groups, and service providers for successful selection, contracting, and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, and BMS outsourcing and procurement policies and procedures. Ensure project success by meeting short-term objectives and adhering to project schedules. Support the Outsourcing team in tasks across outsourcing, alliance management, FSP operations, and financial/resource accountability. Communicate with business partners and internal clients regarding contractual issues as needed. Provide operational expertise, support, guidance, and training to teams on all aspects of outsourced work. Ensure team alignment with related BMS outsourcing strategies. Qualifications & Experience: Minimum of a BA or BS Degree in Legal, Life Science, Business Administration, or equivalent. An advanced degree is a plus. 3 to 5 years of relevant industry experience in clinical development (pharma, biotech, CRO) is required. Experience engaging with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating, and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry. Proven experience in effectively managing key internal and external stakeholders by frequently soliciting input and incorporating feedback into processes as appropriate. Effective management of cross-functional, multi-cultural teams and demonstrated ability to work and influence within a matrix structure. Proven time management skills with the ability to manage multiple priorities and take on new initiatives and improvement efforts. Demonstrates a high level of adaptability in dealing with ambiguous and complex work environments, balancing multiple demands in a responsive and professional manner. Ability to sustain high levels of performance in a constantly changing environment. Show more Show less

Position Summary: Provide management for the Patient Safety support for outcomes of internal audits of Pharmacovigilance (GVP) systems/processes, business partner audits of GVP processes, GVP deviation investigations and PV Quality Management System (QMS) support. Duties/ Responsibilities : Manage outcomes of GVP audits in terms of post-evaluation to ensure that corrective and preventative actions are authored and implemented in a timely manner. Support post-evaluation response to the GVP elements of GCP, GMP and GDP audits to ensure that corrective and preventative actions are authored and implemented in a timely manner for items impacting the GVP system. Effectively collaborate with external quality and compliance organizations (i.e. R&D Quality Assurance) to maintain high standards of quality for the department. Participate and or lead the individual assessments for the identification, risk assessment, investigation, and closure of GVP deviations for issues impacting the GVP system. Additionally, contribute to the suggested remediation efforts. Monitor CAPA, Effectiveness Check, Deviation and associated risk triggers for reporting to PV Quality Council and associated functional management. Define appropriate escalation process to ensure overall performance of the program. Manage the trending and analysis of quality issues from various sources for items impacting compliance and quality. Concisely summarizes and effectively communicates the result of analysis and intelligence with stakeholders as appropriate to address issues and prevent recurrence of quality and compliance issues. Suggest improvements to the review of departmental standard operating procedures related to CAPA management, effectiveness checks, deviation management and GVP QMS. Represent the PV Compliance and Quality Risk Management team partnering with other internal Research & Development/BMS stakeholders to align to principles of GVP QMS as it relates to CAPA management, effectiveness checks and deviation management. Ensure all data supporting deviations and open CAPA within the Pharmacovigilance System Masterfile (PSMF) is current and of high quality to enable applicable sections to be generated in a timely manner. Escalates issues to respective functions and management for evaluation and remediation. Show more Show less

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary Develop and/or revise global procedural documents to support the business unit processes in the Quality Management System (QMS) process framework. Procedural management activities include, but are not limited to, working with subject-matter experts to ensure accurate document content and compliance with health authority regulations and expectations. Key Responsibilities This position is responsible for facilitating global procedural documents across areas of the QMS Framework and in association with electronic systems that support maintaining the QMS. This includes, but not limited, to document authoring, coordination of review and comments resolution, approval, issuance, implementation, periodic review, and retirement. Responsible for compliance assessment of procedural documents against evolving global health authority regulations and health authority inspection observations. Maintain a contemporary knowledge of current industry trends, standards and methodologies as it relates to quality systems and management. Support Global Product Development & Supply organization as the SME for BMS electronic document management system. Support strategic initiatives and continuous improvement projects related to QMS Synthesize feedback from SMEs/procedural document teams to identify and resolve issues in order to accurately document current and future processes Effectively manage projects, escalate issues as necessary and identify/meet key milestones Work with limited guidance to manage the development of global procedural documents and, seek input as needed Team leadership skills that contribute to meeting team goals and resolving complex issues Exercise sound judgment, using a risk-based approach, to ensure compliance with procedural document regulations, practices, and policies Collect metrics to identify trends and take appropriate action Responsible for communication of procedural document status to businesses Qualifications & Experience Education: Minimum of a Bachelor’s degree 5+ years experience in the Biopharm/Pharmaceutical industry with cross-functional experience in one or more areas (i.e. research, analytical, quality, engineering, manufacturing, regulatory CMC, or IT) Experience with demonstrated leadership in quality and/or compliance discipline with in-depth knowledge of cGMP requirements and global health authorities’ regulations Experience/Knowledge: In depth knowledge of cGMP requirements and global health authority regulations with ability to interpret, apply and implement. Strong negotiating and influencing skills in a matrixed organization. Ability to drive consensus, performance and to lead strategically. High level of competency in procedural document writing including the appropriate use of grammar, syntax and organization of ideas Demonstrated ability to work independently and mentor team members. Ability to identify, manage, and/or escalate issues and risks to timelines. Fluent in English, with proven professional working proficiency in English for reading, writing and speaking. Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. #DDHYD #HYBRID Show more Show less

Key Responsibilities: Responsible for managing and reporting of accurate and on time Global Quality metrics for Product Quality Complaints (PQC) in a fast-paced environment that support Tier Councils, Product Quality Complaint compliance & trending across the organization, internal & regulatory audits. Expertise with data management and analysis using electronic software solutions, eg VEEVA, Tableau, SpotFire, and Microsoft Office, with focus on Excel, PowerPoint, and SharePoint. Responsible to maintain a high level of knowledge & understanding of Pharmaceutical/Biologic Quality Assurance, Device Quality Assurance, cGood Manufacturing Practices as applicable in global GMP regulations (including FDA, EMA, MHRA, PMDA, ENVISA, TGA). Responsible to develop & maintain tools and dashboards in support of PQC trending, data surveillance and PQC user support. Responsible to provide PQC data assessments, highlighting trends, signals and risks and business critical information related to Product Quality Complaint data to Quality leadership in a timely fashion. Data & trend assessments will be communicated with stakeholders in a manner commensurate with risk, and enabling appropriate action taking to protect BMS and our patients. Responsible to complete required training and provide support for Product Complaints, Product Surety and Quality Serialization business process activities. You are accountable for other key activities that support the business such as: SharePoint design, data requests/analysis, and providing communication of trends, signals and risks in addition to business critical information to leadership Maintain expertise on PQC data management at BMS, including data sources, data quality, data management, data users Report at appropriate intervals (weekly, monthly, quarterly, year-on-year etc) metrics on key compliance indicators related to PQC performance and procedural compliance (for example on-time closure, increasing/decreasing trends by product/defect category/market etc). Review signals and trends that may present a risk to the organization and/or to our patients. Engage with PQC management and appropriate stakeholders to identify corrective actions. Align with PQC management for escalations to Quality leadership. Provide recommendations and communications based on output from analytical tools and visualizations. Provide risk assessment support for PQC processes, data management and related activities Continuously improve process for assessment and reporting PQC data to drive consistency and understanding of Quality compliance-focused metrics Use Operational Excellence and similar approaches to support the design of metric tools that facilitate proactive discussion and provide visibility/transparency to drive continuous improvement, prioritization and product quality related decisions Lead teams in the development of tools and reports to optimize and standardize metrics Lead collection and review of PQC data in response to health authority requests Lead collection and review of PQC data in support of audit requests (internal and external audits) Lead metrics initiatives related to product quality complaint programs and processes Facilitate and drive standards for communication, management and visibility of product quality support metrics Implementation and timely update of information to ensure content is current and accurate Establish appropriate procedural documents for product quality support metrics Cross train in other areas of the Global Quality organization to assist the business in developing its employees Develop and maintain high quality relationships with key stakeholders Work on multiple projects at one time and manage priorities based on timelines Work independently with a high degree of professional integrity, be highly organized, and be detail-oriented Perform duties as aligned with PQC management Qualifications & Experience: Degree/Certification/Licensure Bachelor of Science degree in data analytics/statistics/biostatistics, engineering, chemistry, biology, or other quantitative field. Advanced degree preferred. Required Competencies: Fluent in English, with proven professional working proficiency in English for reading, writing and speaking Excellent communication with management, peers, and other functional areas Excellent ability to analyze data to extract useful information and trends, and to translate data to effective messaging to stakeholders and leaders supporting effective decision-making Ability to work well cross-functionally with stakeholders Ability to influence positively in a matrix environment Proven ability to understand complex processes/problems and propose alternate solutions Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders Demonstrated Enterprise mindset to be able to think and act across functions and divisions Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives Excellent teamwork, interpersonal, and communication skills, with the ability to communicate and collaborate with employees and management at all levels and through various formats Demonstrated strategic thinking capability and ability to balance conflicting priorities Ability to provide innovative ideas or alternatives that create value including seeking new information and external insights without compromising compliance Ability to clearly articulate analytical needs to functional partners Experience – Responsibility and minimum number of years: A minimum of 5 years of experience in a data analytical role, or in a Quality role where data analytics was a key component in the pharmaceutical/ biotech/ device industry Strong working knowledge/experience with systems such as QMS, SAP/ERP, Veeva Experience with understanding how to respond to trend signals within the context of quality surveillance Strong problem solving skills are required Strong program and project management Ability to manage multiple, simultaneous projects Thorough understanding of Quality Risk Management Mastery of relevant Quality compliance processes and regulations Understanding of technical areas related to pharmaceutical and/or biological manufacturing, chemical and/or biochemical analyses, microbiological Show more Show less

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Project Management Office Manage budget, scopes, purchase orders (POs), and invoices in the BMS business systems. Maintain and update budget trackers regularly in COMPASS Handle SAP activities including invoice tracking and approval. Facilitate effective communication and collaboration between Finance teams, IT, and other stakeholders throughout project lifecycle. Develop and maintain comprehensive project plans, timelines, and resource allocation schedule Monitor project progress, identify risks, and implement mitigation strategies Create and maintain project documentation, including requirements, status reports, and executive summaries Support the evaluation and implementation of emerging technologies in finance processes Relationship management and collaboration Build and maintain relationships at all levels throughout the organization, with Hyderabad Hub, global S&O, global Finance leadership and medical PMs Build an external network to ensure regular exposure to new and best practices, technologies, and process governance standards Hold self and others to timelines, quality, and accuracy. Risk management Anticipate needs, assess and manage business risk taking; escalate issues that may impact management reporting process globally; manage through times of crisis and ambiguity Bachelor s degree in business administration, Finance, Accounting, Information Technology, or related field 4-7+ years of experience, with at least 2+ years in a transformation environment Strong understanding of end-to-end finance processes, including both FP&A and Controllership functions Experience in the pharmaceutical or life sciences industry Knowledge of enterprise finance systems (e.g., SAP, Oracle, Hyperion) Scrum Master or Agile certification Experience with process automation tools and technologies Six Sigma certification (Green Belt) Experience with shared service center transformations Experience with Agile and traditional project management methodologies Expert-level proficiency in Microsoft Office Suite and project management tools Experience working for a multinational organization and working with colleagues internationally, especially in a highly collaborative manner and culture Experience with global teams and/or centers of excellence Proficiency in English language Ability and willingness to travel internationally as needed Support Department initiatives and special projects including but not limited to: Newsletters, Lunch and Learns, Dept meetings, Offsites, as directed by S&O Leads Project management software (e.g., Microsoft Project, Jira, Trello) Business process mapping tools Data visualization tools (e.g., Power BI, Tableau) Understanding of RPA (Robotic Process Automation) concepts Knowledge of accounting and financial systems Understanding of internal control frameworks (e.g., SOX) Familiarity with SQL and basic programming concepts Experience with ERP systems and financial applications With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. The Manager, Alliance Accounting, is a key member of the Global Finance organization, supporting the management team in the global consolidation, financial, and external reporting processes. This role involves interacting with our external partners and BMS colleagues across various regions and functions to manage our license and collaboration agreement obligations. The position offers substantial exposure to pharmaceutical industry accounting and reporting practices, enhancing financial reporting and analysis skills, communication skills, and leadership abilities in a global environment. Duties and Responsibilities: Execute monthly and quarterly accounting processes, collaborating with external and internal stakeholders by preparing journal entries, performing balance sheet reconciliations, reporting of results to external and internal partners and managing cash activity. Prepare quarterly royalty statements in compliance with license and collaboration agreements, ensuring accuracy and meeting reporting deadlines. Identify and resolve discrepancies or issues related to royalty reports and payments. Participate in cross-functional projects and support other finance organization teams as needed. Provide support for internal and external audits and control tests related to royalties and alliance practices. Champion process improvement and automation initiatives within the controllership organization Analyze and implement changes to corporate reporting systems, processes, reports, and controls to align with the company s evolving business models. Requirements: 5+ years of accounting experience, preferably with a focus on US GAAP. University degree in Accounting CA (Chartered Accountant) required Public company experience strongly preferred. Exposure to collaboration and license arrangements preferred. Advanced Microsoft Excel skills, including the ability to manipulate large data sets. Experience in the Pharmaceutical/Life Sciences/Biotech industry preferred. Strong analytical skills and critical thinking skills. Ability to prioritize and manage workloads in a complex work environment. Team player with a process-oriented mindset. Accountable, self-motivated, and results-oriented, with a strong sense of ownership. Highly organized, accurate, and detail-oriented, with the ability to manage multiple projects simultaneously, work under pressure, and meet tight deadlines. Excellent communication skills, with the ability to work well with all levels and departments within the company. Working knowledge of SAP and SAP Business Consolidation Systems preferred. Ability to thrive in a fast-growing environment with frequent changes, requiring strong multi-tasking skills and flexibility. With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Data Scientist II, BIA GPS India Operations Summary The Data Scientist II will play a crucial role in supporting operational analytics across GPS to ensure products continue to serve most pressing GPS analytics needs, with potential opportunities to build new advanced analytics capabilities such as predictive modelling, simulation, and optimization. The Data Scientist II should have a strong interest in solving business problems, and an eagerness to work on all parts of the analytics value chain, from partnering with IT on data pipelines to operationalizing analytics in the service of our patients around the world. Roles & Responsibilities Conduct analysis and interpretation of complex data sets to derive meaningful insights and recommendations based on an understanding of GPS priorities, critical issues, and value levers. Collaborate with stakeholders to identify business problems, goals, and KPIs to to design, establish and maintain data pipelines, models and business facing reports and dashboards. Design, develop, and implement a broad array of GPS analytics that solve complex problems in a computationally efficient and statistically valid manner. Identify and implement enhancement and automation of high-value analytics while ensuring they continue to function efficiently. Collaborate proactively with IT teams to develop and enhance data infrastructure, data pipelines, and analytical tools for efficient data collection, processing, and analysis. Prepare reports, dashboards, and presentations to communicate analyses to stakeholders at various levels of the organization. Follow technical best practices in building, maintaining, and enhancing analytics output with scalable solutions, including code version control, pipeline management, deployment, and documentation. Provide training, guidance, and mentorship to junior analysts and team members when required. Work hours that provide sufficient overlap with standard east coast US working hours. Skills and competencies Strong analytical thinking and problem-solving skills with the ability to analyse complex data sets and draw meaningful conclusions. Agile problem-solving ability and desire to learn new things and continuously improve. Proficiency in statistical analysis techniques and methodologies. Strong project management skills and the ability to work independently or as part of a team. Solid understanding of digital analytics tools and platforms and version control. Strong communication skills with the ability to present complex information to non-technical stakeholders in a clear manner. Strong business acumen and strategic thinking, with the ability to translate analytical findings into actionable insights and recommendations. Experience Bachelor's or Master's degree in an analytical, engineering, operations research or scientific discipline. Proven experience (typically 3-5 years) in a data and analytics role, including direct development experience. Experience working with large datasets, data visualization tools, statistical software packages and platforms (specifically R, Python, advanced SQL, Domino, AWS, GitHub, dbt, Tableau) Experience with major GPS applications (SAP, Oracle, LIMS, Infinity, MES) is a plus. Experience with biotech product development, manufacturing operations, supply chain, and quality control is a significant plus. Experience in the biopharma industry a plus. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Show more Show less

About Bristol Myers Squibb: At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Key Responsibilities Functional and Technical: QA Review and approval of validation deliverables associated with various BMS enterprise systems including but not limited to clinical study databases electronic Case Report Forms (eCRF), enterprise commercial manufacturing systems such as electronic laboratory notebooks and manufacturing execution systems, and various VEEVA Vault based configurations. Ensure adequate and timely quality assurance / regulatory compliance support Provide support during regulatory agency and third party inspections Research new technologies, understand existing processes, and reference recognized standards and frameworks Pursue continuous professional development through company paid internal/external training, certifications and/or continuing education. Identify opportunities for continuous improvement Adherence to BMS Core Behaviors Conduct risk & impact assessment to determine the extent of validation and qualification and ensure right sized validation effort for programs Demonstrate critical thinking around interpreting business and industry challenges and recommending best practices-based solutions to improve products, processes, systems Implement organizational IT controls in accordance with applicable regulations and the ability to evaluate and understand the impact of new regulations and requirements Review Periodic Review assignments completions for applications in a timely manner Support responses to application CAPAs and Audits as they relate to health authority investigations and internal audits in a timely manner-in coordination with multiple stakeholder teams Qualifications & Experience: B.E./B.Tech. or equivalent in computer science, engineering, life science field A minimum of 5-7 years of experience in Quality Assurance, IT Compliance and computer systems validation (CSV) in the pharmaceutical industry, including at least 3 years of managing/overseeing IT Compliance and CSV projects Candidate must have a strong understanding of 21 CFR Part 11, EU Annex 11, Data Integrity principles, GAMP and Agile methodologies. Additionally, good understanding of Computer Software Assurance principles desired. Understanding of quality risk-management concepts (ICH Q9) preferred Proven experience in the interpretation and understanding of GxPs for the controlled management of electronic records and signatures Previous experience as a computer system validation / quality assurance / quality control analyst for a life sciences company regulated by the FDA (or equivalent) preferred Familiarity with the drug development process from discovery through to regulatory filing and approval of drug applications as well as commercial manufacturing processes Experience with driving validation strategies across across the end-to-end product lifecycle as well as experience with widely used IT Enterprise platforms (SAP, Veeva, ServiceNOW etc.) General knowledge of IT applications, IT infrastructure, architecture of computer systems including SaaS, IaaS as well as networks, operating systems, databases, and software tools Candidate must have strong knowledge of IT testing practices and methodologies in the pharmaceutical GxP space-and good working knowledge of tools like ALM and Valgensis Ability to make decisions that impact own work and other groups/teams and works with minimal supervision Ability to support various projects, create and work within internal timeliness, solve problems, deliver on commitments and utilize interpersonal skills in a cross-functional team Demonstrates openness to learning and developing. Takes a responsibility for their own and team’s development and growth Demonstrates an understanding of factors driving team performance and how they contribute to?the team's overall success Strong sense of ethics, diplomacy and discretion Commitment to Quality Fluent in English, with proven professional working proficiency in English for reading, writing and speaking. including the ability to deliver clear and articulate presentations Show more Show less

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Data Scientist II, BIA GPS India Operations Summary: The Data Scientist II will play a crucial role in supporting operational analytics across GPS to ensure products continue to serve most pressing GPS analytics needs, with potential opportunities to build new advanced analytics capabilities such as predictive modelling, simulation, and optimization. The Data Scientist II should have a strong interest in solving business problems, and an eagerness to work on all parts of the analytics value chain, from partnering with IT on data pipelines to operationalizing analytics in the service of our patients around the world. Roles & Responsibilities: Conduct analysis and interpretation of complex data sets to derive meaningful insights and recommendations based on an understanding of GPS priorities, critical issues, and value levers. Collaborate with stakeholders to identify business problems, goals, and KPIs to to design, establish and maintain data pipelines, models and business facing reports and dashboards. Design, develop, and implement a broad array of GPS analytics that solve complex problems in a computationally efficient and statistically valid manner. Identify and implement enhancement and automation of high-value analytics while ensuring they continue to function efficiently. Collaborate proactively with IT teams to develop and enhance data infrastructure, data pipelines, and analytical tools for efficient data collection, processing, and analysis. Prepare reports, dashboards, and presentations to communicate analyses to stakeholders at various levels of the organization. Follow technical best practices in building, maintaining, and enhancing analytics output with scalable solutions, including code version control, pipeline management, deployment, and documentation. Provide training, guidance, and mentorship to junior analysts and team members when required. Work hours that provide sufficient overlap with standard east coast US working hours. Skills and competencies Strong analytical thinking and problem-solving skills with the ability to analyse complex data sets and draw meaningful conclusions. Agile problem-solving ability and desire to learn new things and continuously improve. Proficiency in statistical analysis techniques and methodologies. Strong project management skills and the ability to work independently or as part of a team. Solid understanding of digital analytics tools and platforms and version control. Strong communication skills with the ability to present complex information to non-technical stakeholders in a clear manner. Strong business acumen and strategic thinking, with the ability to translate analytical findings into actionable insights and recommendations. Experience Bachelors or Masters degree in an analytical, engineering, operations research or scientific discipline. Proven experience (typically 3-5 years) in a data and analytics role, including direct development experience. Experience working with large datasets, data visualization tools, statistical software packages and platforms (specifically R, Python, advanced SQL, Domino, AWS, GitHub, dbt, Tableau) Experience with major GPS applications (SAP, Oracle, LIMS, Infinity, MES) is a plus. Experience with biotech product development, manufacturing operations, supply chain, and quality control is a significant plus. Experience in the biopharma industry a plus. With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Key Responsibilities Collaborate closely with the business and vendor to provide operational support for system incidents and problems and manage escalations for the supported manufacturing application s . Supporting the business team's interaction with the vendor for enhancements and testing of new patches, third-party BMS software, and upgrades. Participate and collaborate in business meetings with the site and enterprise team, including weekly and monthly operational, COP (Community of Practice), and other relevant meetings . Ensure the Service Now processes, including service support and approval groups, are accurate and current. Collaborate with other members of the IT and business teams to develop and implement business and IT procedures. Work both independently and in a team environment. Work with the local manufacturing and above site teams to raise cost demands and ensure new licenses and renewals are budgeted, requested and processed for the coming year. Support Cyber-Security for periodic review of security reports and audits. Qualifications & Experience Bachelor's degree in Information Technology , Computer Science, Engineering, Life Science, or related field and 2-3 years of relevant experience. Applied knowledge of computerized systems and Systems Development Life Cycle." Knowledge of SaaS systems from planning, implementation, and system release. Ability to work in a diverse work environment, manage multiple priorities, be self-directed. " Excellent written and communication skills are required . " Candidate must have a flexible and creative work style with a goal of attaining excellence. " Ability to work across global sites and cultures. Preferred domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how IT tools and systems support them. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Show more Show less

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Key Responsibilities Accountable for the development and support high-quality software products used by Pharmaceutical Development and Global supplies within GPS. Collaborate with Business and IT Plan functions to develop solutions for business problems including defining business requirements, provide project timelines and budget, develop acceptance criteria, testing, training, and change management plans. Contributes heavily towards developing a plan for development activities and translates those into actionable projects. These include releases, required modifications and discretionary enhancements to support the application life cycle. Collaborate directly with the business clients, IT Business Partners, and other IT functions on delivery of digital capabilities. Take complete ownership of releases from design till deployment and successful production run. This includes coordination with Ops team to deploy applications to various environments. Qualifications Experience: Have a strong commitment to a career in technology with a passion for healthcare. Strong communication still, ability to understand the needs of the business and commitment to deliver the best user experience and adoption. 3+ years of software development experience in full SDLC process, involving Analysis, Design, Development, Testing, and production. Proven experience as a full stack developer or similar role Learn, design, and implement new technologies. Have experience leading and mentoring small teams of highly skilled technical developers. Experience in designing and implementation of business-critical applications within AWS ecosystem. Experience in Cloud platforms such as AWS, Azure, GCP. Experience as a Python/node.js developer Strong knowledge of front-end technologies such as HTML, CSS, JavaScript, and React.js Strong knowledge of relational database technologies such as MySQL, SQL Server, Oracle, and PostgreSQL Strong knowledge of NoSQL databases, such as MongoDB, Amazon DynamoDB, and Cassandra Knowledge of source code repositories like SVN, GitHub, Bitbucket. Knowledge of design and implementation of N- Tier application in both cloud and on-prem environments. Ideal candidates would also have: Have a strong commitment to a career in technology with a passion for healthcare. May lead initiatives related to continuous improvement or implementation of new technologies. Works independently on most deliverables. Participates in decision making and brings a variety of strong views and perspective to achieve team objectives. Knowledge of Software Development Lifecycle (SDLC) and computer systems validation (CSV) Ability to quickly learn new technologies and incorporate them into a solution. Knowledge of Project Management skills, and experience with agile and scrum methodologies

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Position Summary The Project Analyst will support Portfolio and PMO governance lead in providing financial management, Operational oversight and Strategic insights that optimize the services GPS IT function provides our customers. He/She will assist in overseeing the health and performance of GPS IT projects . Closely monitoring, analyzing data, actuals, forecasting, and advising on opportunities that increase the financial position and/or operational efficiencies of the organization. Support Portfolio Governance lead to proactively identify risks and barriers to project goals and monitor the overall health of the portfolio and drive initiatives to optimize. He/She will support the development of reporting capabilities for GPS IT to provide analytics that contribute to developing and implementing improvements that optimize the performance across GPS IT function. On demand and periodically provide metrics and data for consumption by Portfolio Governance in reporting progress to GPS IT and IT PMO Leadership. Responsible for development of reporting including actuals, resource allocations for projects, and cross-functional alignment opportunities. Produce reports and statistics of the Portfolio and PMO that ensure transparency & predictability of execution & financial performance. This role will support financial planning, budgeting, forecasting through each budget cycle and develop reporting capabilities for GPS IT functions to support transparent financial management. He/She will support the organization through technical expertise, financial analytics, and operational excellence capabilities to drive positive outcomes and data improvements. Promote opportunities for improvement that will streamline and automate operations Collaborate with Delivery leads as required on transactional execution of the projects. He/She will assist the Project Managers for project coordination activities. Position Responsibilities Supports to measure and track qualitative and quantitative benefits realization from investments. Assist in the development and maintenance of project management processes, tools, and templates. Support project managers in project planning, tracking, and reporting activities. Collect and analyze project data, ensuring accuracy and completeness. Prepare regular reports, Executive Slides dashboards to provide project status updates to stakeholders. Conduct periodic project audits to ensure compliance with established processes and guidelines. Creating frameworks to collect, cleanse and consume data into our target reporting tools/repositories. Identify actionable results through data correlation findings. Support ad-hoc projects and requests that are assigned to the GPS IT PMO function. Research, identify and resolve root causes driving financial variances. Assist in the development and implementation of process improvement initiatives within the PMO. Stay updated with industry trends and best practices in project management, contributing to the continuous improvement of the PMO. Identify and communicate project risks and issues, assisting in the development of mitigation strategies. Collaborate with project teams to ensure adherence to project management standards and best practices. Assist in the development and implementation of process improvement initiatives within the PMO. Desired Experience Qualifications And Experiences A bachelor's degree or higher or equivalent experience is required. Field of study in mathematics, statistics, Business Administration, Project Management or in computer science and information management are preferred. Proven experience as a Project Analyst or in a similar role, preferably in a fast-paced environment. Experience translating and correlating complex/disparate data points into summarized consumable material. Ability to identify and improve the quality of data used in analytical reporting. Good understanding of project management financials, methodologies and processes. Proficiency in project management tools and software (e.g., Microsoft Project, JIRA, Service Now, PowerBI, Excel, MPP, Spotfire,Azure DevOps). Experience with software development methodologies and requirements gathering techniques such as Agile, (Scrum, AUP, SAFe etc.) and Waterfall is preferred. Skills Desired Proficiency in Excel, including advanced functions, formulas, and data manipulation techniques. Strong experience in developing and implementing macros to automate tasks and improve productivity. Strong analytical and problem-solving skills, with the ability to interpret and present data effectively. Strong communication and collaboration skills to effectively work with cross-functional teams. Demonstrated success working in a matrix team structure to drive collaborative outcomes that meet organizational objectives. Self-motivated with validated personal integrity, judgement and professional maturity and ability to collaborate. Confirmed ability to use structured problem solving and available tools to quickly evaluate problems, identify root causes, create action plans, assess impact and develop resolution options. Strong communicator via all media collaboration technologies (SharePoint, MS Teams, etc.) and presentations written, emails, verbal - with a wide variety of audiences. Excellent teamwork and interpersonal skills, with the ability to communicate and collaborate with employees and management at all levels. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Show more Show less

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . Position Summary- This is a global role which supports the Patient Safety (PS) Mission and Vision through understanding the impact of daily work on all stakeholders of Safety Management Plans (SAE MP's) and Pharmacovigilance Agreements (PVA's).This role provides oversight of quality and process optimization working with multiple global stakeholders across PS and external functions to ensure business critical support to the management of and reporting associated with SAE MPs and PVAs. Major responsibilities will be the drafting, review, negotiation, execution and maintenance of SAE MPs and PVAs as assigned. Duties/Responsibilities Demonstrate strong teamwork skills to ensure accurate production of SAE MPs and PVAs including the processes, procedures, and best practices are consistent across PS and that regulatory requirements are met in a timely manner and with high quality Periodically review and update SAE MPs and PVAs per internal process Builds and maintains strong relationships with other BMS functional areas to complete and facilitate implementation of SAE MPs and PVAs Identifies ways to improve productivity and quality standards for SAE MP and PVA-related deliverables and actively participates in efforts to remedy non compliance situations Review and evaluate integrity of CRO SAE management processes for inspection readiness. Apply knowledge of specific work practices, Standard Operating Procedures (SOP), and regulations to maintain oversight of SAE MPs and PVAs and ensure successful execution of tasks. Engage and develop working relationships with Preferred CROs and Business Partners to ensure alignment with BMS processes. Maintain a customer service focus with internal and external colleagues. Take personal initiative by proactively identifying innovative ways to accomplish tasks and drive toward process efficiencies. Utilize effective organizational skills to prioritize deliverables to accomplish work in established timeframes. Contribute to continuous quality improvement process through projects and other related departmental initiatives. Develop expertise in associated applications and web systems (e-TMF, Veeva Vault, PVA and SAE MP Management system. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Show more Show less

About Bristol Myers Squibb: At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. The Manager, Alliance Accounting, is a key member of the Global Finance organization, supporting the management team in the global consolidation, financial, and external reporting processes. This role involves interacting with our external partners and BMS colleagues across various regions and functions to manage our license and collaboration agreement obligations. The position offers substantial exposure to pharmaceutical industry accounting and reporting practices, enhancing financial reporting and analysis skills, communication skills, and leadership abilities in a global environment. Duties and Responsibilities: Execute monthly and quarterly accounting processes, collaborating with external and internal stakeholders by preparing journal entries, performing balance sheet reconciliations, reporting of results to external and internal partners and managing cash activity. Prepare quarterly royalty statements in compliance with license and collaboration agreements, ensuring accuracy and meeting reporting deadlines. Identify and resolve discrepancies or issues related to royalty reports and payments. Participate in cross-functional projects and support other finance organization teams as needed. Provide support for internal and external audits and control tests related to royalties and alliance practices. Champion process improvement and automation initiatives within the controllership organization Analyze and implement changes to corporate reporting systems, processes, reports, and controls to align with the company’s evolving business models. Requirements: 5+ years of accounting experience, preferably with a focus on US GAAP. University degree in Accounting CA (Chartered Accountant) required Public company experience strongly preferred. Exposure to collaboration and license arrangements preferred. Advanced Microsoft Excel skills, including the ability to manipulate large data sets. Experience in the Pharmaceutical/Life Sciences/Biotech industry preferred. Strong analytical skills and critical thinking skills. Ability to prioritize and manage workloads in a complex work environment. Team player with a process-oriented mindset. Accountable, self-motivated, and results-oriented, with a strong sense of ownership. Highly organized, accurate, and detail-oriented, with the ability to manage multiple projects simultaneously, work under pressure, and meet tight deadlines. Excellent communication skills, with the ability to work well with all levels and departments within the company. Working knowledge of SAP and SAP Business Consolidation Systems preferred. Ability to thrive in a fast-growing environment with frequent changes, requiring strong multi-tasking skills and flexibility Show more Show less

About Bristol Myers Squibb: At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary: The GPS Data & Analytics Sr. Software Engineer (AI/ML) role is accountable for developing AI/ML & Gen AI Solutions, you will play a pivotal role in designing, developing, and deploying advanced AI/ML Models & Gen AI solutions in Global Product Development and Supply – Data and Analytics Enablement organization. Position Responsibilities Key Responsibilities: Design, develop, and implement machine learning models and AI algorithms to solve complex business problems. Implement Retrieval-Augmented Generation (RAG): Design and develop systems that combine retrieval-based methods with generative models to enhance the accuracy and relevance of AI-generated content. Utilize Vector Embeddings: Develop and optimize vector embeddings for various applications, including semantic search, recommendation systems, and natural language understanding. Leverage LLMs: Integrate and fine-tune ChatGPT or similar large language models to create conversational AI solutions, enhancing user interactions and automating customer support. Collaborate with other engineers to understand requirements and deliver high-quality solutions. Optimize and fine-tune machine learning models for performance, scalability, and accuracy. Conduct research and stay up-to-date with the latest advancements in AI and machine learning technologies. Worked/ Posses Knowledge on Agentic Design Patterns & any one of the frameworks like Bedrock, Crew AI, Langsmith, Agnos, Autogen, etc Mentor and guide junior engineers, providing technical leadership and fostering a culture of continuous learning. Participate in code reviews, design discussions, and contribute to best practices for software development. Develop and maintain documentation for AI/ML models, algorithms, and processes. Work with large datasets, perform data preprocessing, feature engineering, and model evaluation. Deploy and monitor machine learning models in production environments, ensuring reliability and robustness. Experience with natural language processing (NLP), computer vision, or other specialized AI domains. Show more Show less