29 Pharmaceutical Manufacturing Jobs

As a Production Manager at Kanath Engineering, you will play a crucial role in overseeing and managing the production processes at our Atgaon site. Your responsibilities will involve ensuring the efficiency of operations, maintaining quality assurance standards, and upholding safety protocols. You will be tasked with planning and organizing production schedules, collaborating with various departments, supervising production staff, and optimizing resource allocation to achieve production targets effectively. To excel in this role, you should bring a wealth of experience in production management and a strong background in process optimization. A solid grasp of manufacturing standards and safety protocols is essential, along with proficiency in utilizing production management software and tools. Your exceptional leadership qualities, adept team management skills, and effective communication abilities will be key assets in fulfilling the responsibilities of this position. Moreover, your ability to swiftly analyze and address production-related challenges will be invaluable. While prior experience in the pharmaceutical manufacturing industry is advantageous, it is not mandatory. However, a Bachelor's degree in Engineering, Manufacturing, or a related field is required to be considered for this opportunity. If you are driven by the prospect of making a significant impact in the pharmaceutical industry and possess the qualifications and skills outlined above, we encourage you to apply for this exciting position at Kanath Engineering.,

As a valued member of our team, you will play a crucial role in ensuring the delivery of safe and effective products to patients. Your dedication to quality, coupled with our customer-oriented culture, rooted in science and compliance, will directly impact patient care. You will contribute to upholding a quality culture that evolves to meet patient needs, guaranteeing that our products meet the highest safety and efficacy standards. In this role, your responsibilities will include creating, reviewing, and approving test method transfer and validation protocols, reports, and equipment qualification records. You will maintain compliance with Good Manufacturing Practices in Quality Control and Stability laboratories, support media preparation, handle Bio ball cultures, and conduct microbiology-related investigations. Additionally, you will perform testing on various samples, manage Laboratory Information Management System builds, review laboratory data, serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and provide training to junior colleagues. To excel in this role, you must possess a Master's degree in microbiology with a minimum of 6 years of relevant experience. Strong technical skills in method validation and testing, along with experience in microbiological testing of water, are essential. A deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations, coupled with attention to detail and robust knowledge of quality systems, will be key to your success. Effective written and verbal communication, interpersonal skills, and familiarity with research unit clinical and analytical laboratory environments are also necessary. Preferred qualifications include relevant pharmaceutical experience, a strong understanding of computer system hardware, infrastructure, and networks, as well as experience with Laboratory Information Management Systems (LIMS). Proficiency in data analysis and interpretation, knowledge of regulatory requirements and guidelines, strong problem-solving abilities, effective time management, organizational skills, and the ability to mentor and train junior colleagues are considered advantageous. Your work location will be on premise, and Pfizer is proud to be an equal opportunity employer that complies with all applicable equal employment opportunity legislation in each jurisdiction where it operates. Join us in upholding quality assurance and control to make a meaningful difference in patient care.,

A well known Special purpose machinery manufacturing company located in Turbhe MIDC,Navi Mumbai is looking for suitable candidate in the role of Industrial Automation Engineer Desired Candidate : Male,BE/B.Tech in Electrical Engineering or equivalent with knowledge of Industrial Automation Proven experience in working with PLC systems, VFDs/drives , PLC Programming Strong understanding of safety standards and regulatory requirements in the pharma environment welcome Electrical design and automation, preferably in the machine-building industry Residing in Navi Mumbai or adjoining areas Age below 50 years Key Responsibilities : Design, develop, and implement electrical systems for fully automated pharmaceutical machinery. Program and troubleshoot PLC systems , drives , and HMI interfaces (e.g., Siemens, Allen-Bradley, Mitsubishi, etc.). Collaborate with mechanical and software engineers in the design and integration of automation systems. Work closely with the production and commissioning teams to ensure seamless equipment functionality. Prepare electrical documentation including wiring diagrams, cable schedules, and BOMs. Ensure compliance with GMP, FDA, and other pharma-industry-specific standards. Provide technical support during installation, commissioning, and after-sales service. Coordinate with clients and internal stakeholders; effective communication and interpersonal skills are essential. Salary : As per the industry standards Holiday : Sunday and Alternate Saturday If interested kindly mail us your updated resume with salary details and notice period to os.consultancy@hotmail.com

As the Senior Vice President, Global Head of Commercial Operations at our Global CDMO, you will play a pivotal role in driving key commercial aspects of the business and leading strategic initiatives to ensure continued growth and success. Your responsibilities will involve overseeing various commercial functions, aligning strategies with growth objectives, and building strong client relationships across multiple markets. Your primary focus will be on developing and executing a comprehensive global commercial strategy that aligns with corporate goals and drives revenue growth. You will collaborate with internal teams such as Business Development, Finance, and Regulatory Affairs to enhance operational efficiency and effectiveness. Additionally, you will be responsible for managing client relationships, ensuring customer needs are met, and implementing customer-centric strategies to foster long-term partnerships. In this leadership role, you will oversee key functions including Commercial Strategy, Proposal Management, Marketing, Pricing, and Analytics. You will drive initiatives to optimize business processes, enhance pricing strategies, and improve commercial operations. Your role will also involve leading marketing and lead generation efforts to increase brand awareness and customer acquisition. As the Global Head of Commercial Operations, you will be instrumental in managing the sales pipeline, aligning proposals with market demands, and implementing competitive pricing models based on market analysis. You will lead strategic projects aimed at improving commercial performance and decision-making, while fostering a culture of continuous improvement within the commercial team. Furthermore, you will play a key role in talent development by building and mentoring a high-performing team, establishing onboarding programs, and implementing learning and development initiatives. Your leadership will be crucial in driving operational excellence, enhancing customer satisfaction, and supporting the long-term growth objectives of our organization. If you are a seasoned leader with over 20 years of experience in commercial operations, sales leadership, or business development within the CDMO or pharmaceutical manufacturing sector, and possess a strong track record of success in a global leadership role, we invite you to join our team at Piramal Pharma Solutions (PPS) and contribute to our mission of providing end-to-end development and manufacturing solutions across the drug life cycle.,

Candidate should be capable of independently executing Turnkey project/ HVAC / Cleanroom / Modular and MEP Projects with specialization in Pharmaceutical Machineries. Should have good team management skill. Required Candidate profile Through knowledge of designing of HVAC/ Modular Partition panels Knowledge of pharmaceutical utilities with detailed knowledge of process and validation. Education UG: B.Tech/B.E. in Any Specialization PG: M.Tech in Mechanical About company A leading Pharma Equipment manufacturing company based out of Mumbai

Role & responsibilities With 5-6 years of experience in sourcing and procurement of pharmaceutical formulations, APIs and Packaging Materials, The position will be accountable for the entire procurement process. Sourcing Vendor development, Price negotiation and procurement. The position is based at Mumbai. Graduates with strong techno-commercial knowledge will be preferred Arranging advance payment to vendor wherever applicable, Co-ordination with logistics for vehicle arrangement for material pick-up wherever applicable, Follow-up, tracking of materials & ensure that material should reach as per given scheduled. Developing and sustaining long-term relationships with suppliers. Travelling to different places as and when required. Arranging samples as per requirement for New Product Development. Arranging DMF/COPP/COA for support to Regulatory Department Interested can Send CV at hr@denamrkpharma.com

SENIOR QUALITY CONTROL ANALYST Job Objective: The Quality Control (QC) Analyst specializing in Method Validation and Method Development is responsible for developing, validating, and transferring analytical methods for pharmaceutical raw materials, intermediates, and finished products. The role ensures compliance with regulatory requirements and contributes to continuous improvements in analytical methodologies. Qualifications: Bachelors/Masters degree in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or related field. Experience: More than 8 years of experience in method validation, method transfer, and regulatory compliance within a pharmaceutical QC or analytical development environment. Job Responsibilities: Method Development & Optimization: Develop and optimize analytical methods for assay, dissolution, related substances, and residual solvents using techniques like HPLC, GC, UV-Vis, FTIR. Establish and refine chromatographic conditions, mobile phases, and detection parameters for improved sensitivity and reproducibility. Conduct forced degradation and stability-indicating method development as per ICH Q1A guidelines. Method Validation & Transfer: Perform method validation as per ICH guidelines covering accuracy, precision, specificity, linearity, robustness, and system suitability. Prepare and review method validation protocols and reports. Execute method transfer activities between R&D, QC, and manufacturing sites following GMP requirements. Regulatory Compliance & Documentation: Ensure analytical methods meet US FDA, EU GMP, MHRA, WHO, and other regulatory expectations. Maintain accurate documentation as per Good Documentation Practices (GDP). Support regulatory filings by preparing analytical method validation reports and technical dossiers. Assist in responding to regulatory queries and audits related to analytical methods. Instrumentation & Troubleshooting: Operate and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and dissolution testers. Troubleshoot chromatographic issues related to retention time shifts, peak tailing, and resolution problems. Participate in instrument qualification (IQ/OQ/PQ) as needed. Collaboration & Process Improvement: Work closely with R&D, Manufacturing, and Quality Assurance teams for seamless method transfer. Investigate out-of-specification (OOS) and out-of-trend (OOT) results to identify root causes. Contribute to continuous improvements in analytical techniques and laboratory efficiency. Technical Skills: Strong expertise in HPLC, GC, UV-Vis, FTIR

Job Description: You will be joining a renowned organization, Piramal Group, which has been thriving for three decades through a strategic approach of both organic and inorganic growth. At Piramal Group, we are committed to inclusive growth driven by our core values, ensuring that ethical and values-driven practices are at the forefront of all our endeavors. Equal employment opportunity is a cornerstone of our work culture. All employment decisions are based on merit, taking into account qualifications, skills, performance, and achievements. We are dedicated to providing equal opportunities to all applicants and employees in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions. We also offer reasonable accommodation for qualified individuals with disabilities and those with specific needs related to their religious observance or practice. Join the team at Piramal Pharma Solutions (PPS), a Contract Development and Manufacturing Organization (CDMO) that provides comprehensive solutions throughout the drug life cycle. Our globally integrated network of facilities in North America, Europe, and Asia enables us to offer a wide range of services, including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Additionally, we specialize in the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also caters to the development and manufacturing services for biologics such as vaccines, gene therapies, and monoclonal antibodies, facilitated by Piramal Pharma Limited's investment in Yapan Bio Private Limited. With a proven track record as a trusted service provider across various technologies, we are the preferred partner for innovators and generic companies globally. Job Info: - Job Identification: 9041 - Job Category: Supply Chain - Posting Date: 07/15/2025, 03:58 PM - Apply Before: 07/26/2025, 03:57 PM - Degree Level: Bachelor's Degree - Job Schedule: Full time - Location: Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN,

QA Chemist - API Pharmaceutical Industry.Responsible for monitoring & compliance of Self-Inspection and Quality Audits conducted at site.Responsible for the preparation & monitoring of HACCP & its related activity.

Company Description GLOBELA PHARMA PVT LTD, located in Bharuch district, is an ISO 9001:2015, WHO cGMP accredited pharmaceutical manufacturing company. We specialize in producing high-quality pharmaceutical formulations in various forms such as tablets, capsules, and dry powder ORS. Our products are registered in multiple overseas countries, including Bolivia, Costa Rica, Panama, Venezuela, and Kenya, among others. We have dedicated facilities for contract manufacturing, party-to-party manufacturing, and loan license manufacturing. Role Description This is a full-time on-site role as a Production Manager at GLOBELA PHARMA PVT LTD in Bharuch district. The Production Manager will be responsible for overseeing day-to-day manufacturing operations, ensuring compliance with quality standards, managing production schedules, coordinating with various departments, and optimizing production processes to meet production targets and deadlines. Qualifications Experience in pharmaceutical manufacturing or a related industry Knowledge of cGMP guidelines and quality management systems Strong leadership and team management skills Excellent problem-solving and decision-making abilities Good communication and interpersonal skills Attention to detail and ability to work under pressure Bachelor's degree in Pharmacy, Chemical Engineering, or a related field Prior experience as a Production Manager is a plus,

As a Production Manager, you will be responsible for overseeing and managing day-to-day production operations to ensure quality, cost efficiency, and on-time delivery of products. You will develop and implement production schedules while ensuring compliance with Good Manufacturing Practices (GMP) and USFDA regulations. Your role will involve maintaining regulatory compliance with USFDA, WHO, and other standards, coordinating with the Quality Assurance (QA) team for audits, and ensuring proper documentation of manufacturing processes. Leading and mentoring the production team will be a key aspect of your job to drive optimal performance and regulatory awareness. You will be expected to foster a culture of continuous improvement, accountability, and teamwork. Identifying and implementing process optimizations to enhance productivity, efficiency, and quality will be essential. Collaboration with cross-functional teams such as R&D, Quality Control (QC), and Supply Chain will be required to address production-related issues effectively. In terms of equipment and facility management, you will need to ensure proper maintenance and calibration of production equipment and facilities. Implementing safety protocols to uphold a hazard-free work environment is crucial. Resource planning will also be part of your responsibilities, involving managing raw material inventory and maintaining uninterrupted production. You will also be tasked with preparing and managing the production budget to optimize costs without compromising quality. For this role, a Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Biotechnology, or a related field is required. A minimum of 5-7 years of experience in pharmaceutical manufacturing in a managerial capacity is necessary, along with a proven track record in USFDA-regulated environments and knowledge of cGMP, CAPA, and regulatory submissions. Your technical skills should include a strong understanding of pharmaceutical production processes, familiarity with validation protocols, exceptional leadership and communication skills, as well as strong analytical and problem-solving abilities. The ability to work under pressure, meet tight deadlines, and collaborate effectively with various teams will be critical to your success in this role.,

Walk-in at Matoda Were currently recruiting for multiple positions at our SANAND manufacturing facility. If any role aligns with your experience, please bring your updated resume and walk in during the scheduled drive. Please find our current job requirements and venue details mentioned. Requirement : Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Time and Venue : 12th June 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Walk-in at Matoda Were currently recruiting for multiple positions at our SANAND manufacturing facility. If any role aligns with your experience, please bring your updated resume and walk in during the scheduled drive. Please find our current job requirements and venue details mentioned. Requirement : Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Time and Venue : 12th JULY 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a world where ,Health for all, Hunger for noneis no longer a dream, but a real possibility Were doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining impossible There are so many reasons to join us If youre hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, theres only one choice Executive, Process & Plant safety POSITION PURPOSE: Responsible for Process and Plant safety ensuring minimum risk to people, property and community Responsible for leading Process and Plant safety risk assessments MAJOR TASKS AND RESPONSIBILITIES: Interpret Process and Plant safety policy as laid down by Bayer Group and implement using Best Practices (PPS guidelines) Perform risk assessments for management of change with site management team and provide recommendations for the safe implementation of management of change in line with accepted Bayer guidelines Carry out periodic revalidation to ensure that safety concepts as agreed and documented during previous risk assessments are in place and suggest improvements, if possible, to reduce the risks further using state of the art technology Perform Acceptance safety review to verify that all action items from the detailed safety review revalidation have been implemented Prepare Explosion Prevention and Protection Document (EPPD) to prevent or mitigate explosions which could lead to serious consequences, both on site & off site and carry out technical inspection WHO YOU ARE: A degree in Chemical Engineering/Postgraduate in organic chemistry preferably with first class having total industrial experience of minimum 3 years in chemical/pharmaceutical manufacturing plants Preferably 1/2 yearsexperience in performing PHA and/or as a PHA facilitator for AI manufacturing and/or Formulation set up Communicative and motivating Aptitude for Process and Plant Safety Ever feel burnt out by bureaucracyUs too Thats why were changing the way we work for higher productivity, faster innovation, and better results We call it Dynamic Shared Ownership (DSO) Learn more about what DSO will mean for you in your new role here https://www bayer com/en/strategy/strategy Bayer does not charge any fees whatsoever for recruitment process Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext Please dont rely upon any unsolicited email from email addresses not ending with domain name bayer com or job advertisements referring you to an email address that does not end with bayer com YOUR APPLICATION Bayer is an equal opportunity employer that strongly values fairness and respect at work We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc We are committed to treating all applicants fairly and avoiding discrimination Location: India : Gujarat : Vapi Division: Enabling Functions Reference Code: 847763 Contact Us 022-25311234

Ready to build the future with AI At Genpact, we don&rsquot just keep up with technology&mdashwe set the pace. AI and digital innovation are redefining industries, and we&rsquore leading the charge. Genpact&rsquos AI Gigafactory, our industry-first accelerator, is an example of how we&rsquore scaling advanced technology solutions to help global enterprises work smarter, grow faster, and transform at scale. From large-scale models to agentic AI, our breakthrough solutions tackle companies most complex challenges. If you thrive in a fast-moving, innovation-driven environment, love building and deploying cutting-edge AI solutions, and want to push the boundaries of what&rsquos possible, this is your moment. Genpact (NYSE: G) is an advanced technology services and solutions company that delivers lasting value for leading enterprises globally. Through our deep business knowledge, operational excellence, and cutting-edge solutions - we help companies across industries get ahead and stay ahead. Powered by curiosity, courage, and innovation, our teams implement data, technology, and AI to create tomorrow, today. Get to know us at genpact.com and on LinkedIn, X, YouTube, and Facebook. Inviting applications for the role of Manager or Senior Manager, Regulatory affairs- Responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance and defined regulatory strategies along with the preparation and review of information required for development of regulatory CMC dossiers for commercial products. Responsibilities: . Leading project teams, providing technical guidance, ensuring maintenance of team records and process-related documentation i.e process maps, job aids, project trackers, checklists, etc. . The core responsibility will be to review the authored documents, compare them with source documents, ensure there are no transcription or formatting errors, no quality errors, and ensure compliance with regulatory guidelines. . Maintaining the quality of documents through quality reviews ensuring &ldquoNo Queries received from Health Authorities . Work on authoring CMC documentation for worldwide marketing of pharmaceutical products for initial registration and life-cycle management under the direction of team scientists. . Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. . Ability to lead client meetings and managing project governance. . Deliver on agreed SLAs with clients at contract and account/ project level. Meet all monthly reporting/business metrics/KPIs requirements and manage internal control processes. . Planning the project by understanding the client needs, channelizing appropriate resources, managing project deliverables, training team as well as client on a need-basis and providing solutions in real time. . Improvise the process and outcomes by implementing continuous improvement initiatives leveraging six-sigma methodologies, RPA/AI opportunities for harmonization, simplification, and automation . Assess and communicate potential regulatory risks and propose mitigation strategies. . Ability to prioritize & execute the project according to the project plan/ timelines/ schedules. . Ensure established policies and procedures of the organization/client are followed and ensure compliance. . Work with cross-functional teams to track and follow up outstanding documentation, coordinate project status & report to stakeholders using different communication channels. . Contribute to draft Request for information and/ or Request for proposals for new client/ business opportunities. Provide inputs to project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks. . Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills. . Superior attentiveness to detail & has a strong regulatory background. . Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance). . Demonstrated ability to generate innovative solutions to problems and effectively collaborate with and communicate to key stakeholders. . Demonstrated flexibility in responding to changing priorities, multi-tasking and dealing with unexpected events. . Demonstrated effective leadership, communication, and interpersonal skills. Qualifications we seek in you! Bachelor&rsquos or master&rsquos degree required in science, engineering or related field (advanced degree preferred). Why join Genpact . Lead AI-first transformation - Build and scale AI solutions that redefine industries . Make an impact - Drive change for global enterprises and solve business challenges that matter . Accelerate your career&mdashGain hands-on experience, world-class training, mentorship, and AI certifications to advance your skills . Grow with the best - Learn from top engineers, data scientists, and AI experts in a dynamic, fast-moving workplace . Committed to ethical AI - Work in an environment where governance, transparency, and security are at the core of everything we build . Thrive in a values-driven culture - Our courage, curiosity, and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress Come join the 140,000+ coders, tech shapers, and growth makers at Genpact and take your career in the only direction that matters: Up. Let&rsquos build tomorrow together. Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values respect and integrity, customer focus, and innovation. Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way. Examples of such scams include purchasing a %27starter kit,%27 paying to apply, or purchasing equipment or training.

Who We Are Applied Materials is the global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world like AI and IoT. If you want to work beyond the cutting-edge, continuously pushing the boundaries ofscience and engineering to make possiblethe next generations of technology, join us to Make Possible a Better Future. What We Offer Location: Bangalore,IND At Applied, we prioritize the well-being of you and your family and encourage you to bring your best self to work. Your happiness, health, and resiliency are at the core of our benefits and wellness programs. Our robust total rewards package makes it easier to take care of your whole self and your whole family. Were committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits . Youll also benefit from a supportive work culture that encourages you to learn, develop and grow your career as you take on challenges and drive innovative solutions for our customers.We empower our team to push the boundaries of what is possiblewhile learning every day in a supportive leading global company. Visit our Careers website to learn more about careers at Applied. Unique Opportunity As a Field Service Engineer Lead er , you will play an integral role in supporting the first private semiconductor FAB in India and in building the semiconductor ecosystem within the country. This position offers the prospect of advancing your career alongside the industry while establishing a high-performing team from the ground up. To learn more about life as a Field Service Engineer, visit the Field Service Engineer page. Responsibilities Building the OrganizationResponsible for creating the Field Service Organization, which includes hiring, onboarding, and upskilling talent to meet business requirements. LeadershipProvides direction, coaching, and development for team members. Problem Solving Identifies and resolves technical, operational, and organizational issues. Customer Relationship Management Maintains and develops relationships with customers. Operational ManagementManages financial, manpower , and operational requirements. CommunicationEffectively communicates business progress, goals, and updates. Safety PracticesEnsures appropriate safety practices among team members. Quality ImprovementPromotes processes to reduce cycle time and drive continuous improvement. Additional Requirement Candidates must be willing to relocate to Singapore/Taiwan for up to 6-9 months upon employment and subsequently be based in Ahmedabad, Gujarat after the initial 12 months. Domain Skills Sound Industrial Engineering practices related to the Semiconductor Domain (e.g., preventive and corrective maintenance). Comprehensive understanding of the semiconductor industry, wafer FAB equipment, and chip manufacturing processes. In the absence of semiconductor domain experience, an equivalent background in biotechnology manufacturing or pharmaceutical manufacturing is preferred. Education Bachelors/ Masters in Engineering or Equivalent . Preferably in Mechanical, Electrical, Mechatronics, Industrial, Chemical and M etallurgy . Additional Certifications complementing the Semiconductor, Pharma or Biotechnology domain will be a value add . Applied Materials is an Equal Opportunity Employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.To learn more about our commitment to DEI visit the Applied Materials Inclusion page. Additional Information Time Type: Full time Employee Type: Assignee / Regular Travel: Yes, 25% of the Time Relocation Eligible: Yes Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.

Location- Novo Nordisk Global Business Services (GBS), Ahmedabad, India Department- GCM Operations Drug Product Are you ready to take charge and make a difference in the pharmaceutical industryIf you’re a dynamic person with a passion for quality and operational efficiency, you might be our new Operations Manager. The position is based in Ahmedabad in India and will report directly to GCM organization based in Denmark. Apply today and get life changing career! Apply now! The position As an Operations Manager, you will be responsible for ensuring Novo Nordisk’s interests with regards to short to midterm capacity, compliance, quality, manufacturing readiness and activities at the CMO. You will have a substantial impact on the business with the CMO with regards to strategy input, prioritization and following up on agreed actions and improvements. Your other responsibilities will be to: Responsible for short to midterm capacity, compliance, quality, manufacturing readiness and activities at selected CMOs ensuring timely delivery of products to downstream customers with a strong focus on production performance and quality. Developing and following up on joint KPI’s and creating a robust working relation with the CMOs. Identify and implement changes and process improvements at CMOs in order to create a strong and solid foundation for future growth in this area. Develop new work standards and setups for collaboration between GCM DP and relevant CMO’s delivering aseptic manufacturing activities. Participate in project work to the extent needed to ensure new projects/CMOs enter operations in a satisfactory manner. Approximately 3–5 weeks of travel per year is expected as part of this role. Qualifications To be successful in this role, you should have: Master’s or Bachelor’s degree in Engineering, Pharmacy, or a Supply Chain-related field, with excellent written and verbal communication skills and a strong command of English 10 years of experience within pharmaceutical manufacturing / packaging and cGMP and 5 years of experience with outsourcing or managing global CMOs. Experience in Production, Manufacturing Operations, Project management or Supply Chain management. Experienced in handling Changes, Deviations, and Customer Complaints, with strong knowledge of regulatory guidelines in the pharmaceutical industry, excellent relationship management skills, and a solid understanding of GxP principles. Team player demonstrating collaborative behavior, effective communicator providing clear and timely information to stakeholders, with a technical, analytical, and structured approach to problem-solving. About the Department Global Contract Manufacturing Drug Products (GCM DP) oversees all aspects of commercial external production, including filling, assembly and packaging. We prioritize diversity, encourage empowerment, and pride ourselves with a varied workforce, comprising a range of professional profiles such as project managers, supply chain professionals, specialists and operation managers.

Job Role: Coordinate and ensure timely payment collection from pharma tooling customers across PAN India . Work closely with the Accounts Team/ recovery team for reconciliation, ledger maintenance, advances, and resolving payment-related issues. Conduct regular follow-ups and reviews with Regional Coordination Teams/Field Executives (FEs) to strengthen the collection process. Guide and monitor Collection Coordinators for effective payment follow-up, tracking, and accurate data management. Prepare and maintain reports related to outstanding payments, collection status, and escalation cases. Liaise with customers and internal teams to resolve disputes and ensure smooth financial operations. Skills Required: Strong coordination, follow-up, and negotiation skills. Proficient in Excel, Tally, GST Banking knowledge and SAP . Good knowledge of Collections from the manufacturing/engineering industry/ , and financial documentation. Excellent communication and drafting skills (both verbal and written) and professional drafting ability. Strong analytical and problem-solving abilities.

Job Description: Data Scientist with Pharma Background Role Overview: The Data Scientist will leverage expertise in pharmaceutical manufacturing data, particularly Electronic Batch Records (EBR), to develop predictive models, ensure data integrity, and drive analytics initiatives that enhance manufacturing compliance and efficiency. This role requires collaboration with cross-functional teams including manufacturing, quality assurance, regulatory, and IT to transform raw EBR data into actionable insights aligned with Good Manufacturing Practices (GMP) and Pharma 4.0 initiatives. Core Responsibilities Analyze and interpret large-scale EBR and manufacturing datasets to identify trends, anomalies, and opportunities for process improvement and risk mitigation. Develop and deploy advanced statistical models and machine learning algorithms to predict batch quality outcomes, detect deviations, and optimize production workflows. Ensure data integrity and compliance by working closely with quality and regulatory teams to maintain audit trails, electronic signatures, and documentation standards as per cGMP requirements. Integrate EBR data with other enterprise systems such as MES, LIMS, and ERP to create unified data models supporting end-to-end manufacturing analytics. Collaborate with IT and software developers to implement data pipelines, dashboards, and visualization tools that provide real-time insights to manufacturing and quality stakeholders. Lead efforts in digital transformation projects aligned with Pharma 4.0, including automation, real-time monitoring, and advanced analytics. Communicate complex analytical findings effectively to both technical and non-technical stakeholders to drive data-driven decision-making. Participate in validation and qualification activities for analytics solutions to ensure compliance with regulatory standards. Provide training and support to manufacturing teams to facilitate adoption of analytics tools and foster a data-driven culture. Required Skills and Experience Strong statistical and mathematical background with expertise in data mining, predictive modeling, and causal analysis. Hands-on experience with pharmaceutical manufacturing data, especially Electronic Batch Records (EBR), and understanding of batch production processes. Knowledge of regulatory compliance requirements related to data integrity, cGMP, and audit readiness in pharma manufacturing. Proficiency in programming languages such as Python and/or R for data analysis, modeling, and automation. Experience with cloud platforms (e.g., AWS) and big data technologies for scalable analytics solutions. Familiarity with integrating and analyzing structured and unstructured data from MES, LIMS, ERP, and EBR systems. Ability to manage complex data integration challenges and maintain secure, compliant data environments. Excellent problem-solving skills and ability to work collaboratively across geographies and functions. Prior experience in pharma or biotech industry analytics roles, preferably involving Medical Affairs or manufacturing data analytics. Knowledge of natural language processing (NLP) and advanced visual analytics is a plus. Preferred Qualifications 4+ years of advanced analytics experience, including machine learning and statistical modeling. 7+ years of experience with a strong focus on pharmaceutical data science. Experience in causal inference, AI/ML applications, and predictive modeling in pharma contexts. Familiarity with electronic signature systems, digital audit trails, and EBR software platforms. Strong communication skills to translate analytics into business insights and influence decision-making.

managing & maintaining liquid vial filling lines & lyophiliser. Maintaining cRABS &/or Isolators. Handling Indian, Chinese or European equipment used in the process, Handling , process vessels and other process equipment’s, Working on QMS aspects Required Candidate profile B. Tech- Electric or instrumentation, Should have good Exp in Pharma Process and Production, Should have exposure to regulatory audits such as EU-GMP, ANVISA, INVIMA, USFDA, Good Communication Skill

To ensure that all raw materials (API & excipients) are sampled, tested, and released. Key Responsibilities: 1. Sampling & Receipt 2. Testing & Analysis 3. Documentation & Release 4. Compliance & Audit Readiness 5. Instrument Handling Required Candidate profile Candidate must have experience in handling team of minimum 10 members. Candidate must have experience into routine analysis of raw material and QMS knowledge.

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD – Manufacturing / QMS (Senior Officer / Officer / Executive) Experience - 02 to 07 Years Qualification – B. Pharmacy/ M Pharmacy Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification – BE / B Tech Time and Venue : 14th June 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Driving revenue growth, expanding market presence, building a strong sales team, targets, ensuring high customer satisfaction. Exp in Containment Solution Technologies (CST), Powder Handling Technologies (PHT), Particle Size Technologies (PST). Required Candidate profile Must handle sales Hyderabad and South India . The candidate should hv exp in selling Isolators and pharmaceutical process equipment, including granulation, coating, and liquid manufacturing systems.

Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Manufacturing Engineering MES Good to have skills : NAMinimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 5 to 7.5 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-This position is based at our Kolkata, Bengaluru, Pune, Mumbai, Chennai, Hyderabad and Ahmedabad office.-A full-time 15 years of education is required. Qualification 15 years full time education

ensure the reliable & efficient operation of utility systems (water, gas, electricity & HVAC systems) minimizing downtime & maximizing production Perform routine maintenance & repairs, troubleshoot equipment failure, safety & environmental compliance Required Candidate profile electrical engineer 3+ years' experience as a utility maintenance engineer in a mfg. co Strong knowledge of utility systems - power generation, distribution, water treatment, HVAC, & compressed air