54 Qa Management Jobs - Page 2

Role & responsibilities Lead a team of QA professionals to manage QA oversight to Manufacturing process operations. Provide leadership for lot release, incoming quality, manufacturing, and labs investigations, change control and corrective and preventative action review/approval, manufacturing support, record review/approval, and ongoing projects support etc. Support team by guidance and coaching and provide direction/approval of activities and decisions. Coordinate planned external audits and drive Internal Audit plan and share reports and outcome to the Site Management Team proposing continuous improvement action plan Analyze trends, quality metrics and other data to identify quality and compliance gaps. Manage release of product batches, including owning the QA product release workflow in SAP. Develop and maintain a Quality Management System in accordance with domestic and international regulatory requirements Manage Quality Control related activities regarding all in-process checks, deviations, RM release, and finished product release. Ensure that products conform to specifications and regulatory requirements. Approve or reject all formulations, procedures, specifications, test methods, raw materials, packaging materials, and finished products, including products manufactured at third parties , based on conformance / non-conformance to respective specifications that affect the purity, quality, and composition of each product. Oversee complaint handling, corrective and preventive actions, internal audit program, supplier quality assurance, product inspection and release, equipment calibration, and control of nonconforming material. Maintain Master formulations, Change Control, and history records. Develop & make a master formula for all new registrations. Identify and analyze issues related to in-process manufacturing and resolve them. Maintain and improve product quality by completing product and company system, compliance, and surveillance audits; investigating customer complaints; collaborating with other members of management to develop a new product, and manufacturing and training methods. Responsible for periodic review of SOP s, specification and standard operating procedure. Responsible for trouble shutting of analytical instruments. Responsible for Quality training initiative (GMP) across the site. Candidates must have experience HVAC validations . Candidates must have experience in microbiology sections . Candidates must have experience in handling of BMR, BPR,IPQA. Candidate worked regulatory environment like WHO-GMP, MHRA,EU-GMP etc. Candidates must have experience FDA license registration process Candidates must have experience in dossiers preparation.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. QA Manager What you will do Role Description: In this role you will be serving patients through internal collaboration with Amgen’s global quality teams, manufacturing sites and external engagement with contract manufacturing organizations. You will make key contributions to fulfill Amgen’s missions of serving patients by ensuring supply of high-quality product produced at contract manufacturers to patients. The QA Manager will support implementation and management of quality assurance activities at the Amgen Technology and Innovation Center, supporting oversight and maintenance of external suppliers and contract manufacturers. You will be responsible for leading a team of quality professionals who will be maintaining and approving various quality documents including but not limited tosupplier documentation, analytical results investigations, CAPA and audit records. This role will involve collaboration with various Amgen teams to ensure seamless handoffs between teams Roles & Responsibilities: Oversee a team of approx. 6 staff, ensuring their activities and priorities are managed in a compliant and structured manner. Ensure team members are appropriately qualified and trained to perform needed activities per company procedures. Conduct goal setting, performance reviews, and compensation planning to align with organizational goals. Develop, implement, and maintain quality records in compliance with industry standards, GMP practices, and regulatory requirements. Continuously improve processes to enhance efficiency and quality, by applying lean principles and automation. Develop, monitor and report metrics to senior management to assess the health of the team’s performance. Develop solutions that are thorough, practical, and consistent with functional objectives. Work cross functionally with various Amgen teams and stakeholders to ensure seamless transition of tasks and continuity across groups. Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations. This role may require working in shifts or extended hours within the same shift to support global time zones. What we expect of you Basic Qualifications and Experience: Doctorate degree OR Master’s degree with 4 to 6 years of experience in quality management systems or a related field OR Bachelor’s degree with 6 to 8 years of experience in quality management systems or a related field OR Diploma with 10 to 12 years of experience in quality management systems or a related field. Experience managing staff in a GXP environment Functional Skills: Must-Have Skills: Working foundation in quality assurance roles and proven team leader. Minimum of 6 years working in a cGMP manufacturing environment with a strong understanding of regulatory requirements and expectations. Ability to have a positive impact on others; the ability to affect the behaviors of others by connecting with and inspiring them Good-to-Have Skills: Experience in investigations, project management and trending and analysis Relevant experience in Supplier Management, raw materials, packaging components, and/or device manufacturing. Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes). Proven experience in designing and/or improving processes at conceptual level Desire to partner with internal and external stakeholders across teams Understanding of industry requirements/expectations of a robust Quality Management System and documentation. Soft Skills: Excellent analytical and troubleshooting skills. Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals Strong presentation and public speaking skills. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

• AS9100D and QMS implementation. • Hands on exposure to Wire Harness for Aerospace and Defense QA • RCCA by using 8D, Fish Bone, WHY_WHYs. • People management. • Lean Manufacturing. • FAI as per AS9102. • PFMEA and APQP.

We are looking for a highly skilled and proactive Technical QA Project Manager to lead Quality Assurance initiatives across complex programmes and multi-team work packages. This role requires a strong blend of technical expertise, client-facing capabilities, project management skills, and leadership acumen to ensure the successful delivery of quality solutions, on time and within scope Roles and Responsibilities Mandatory Attributes: A problem-solver with attention to detail and a commitment to quality. A leader who can inspire and influence both clients and internal teams. Comfortable navigating ambiguity and taking ownership of delivery outcomes. Project & Delivery Management: Plan, track, and ensure on-time delivery of QA work packages. Lead daily/weekly stand-ups to monitor progress and resolve blockers. Key responsibilities: Client & Stakeholder Liaison: Serve as the main point of contact for clients and internal teams. Communicate status, risks, and priorities clearly and proactively. Quality Metrics & Reporting: Track QA KPIs (e.g., defect leakage, automation coverage) and deliver regular dashboards and executive summaries to drive improvement. Risk & Change Management: Identify testing risks early and plan mitigation. Assess impacts of scope changes and adjust QA plans accordingly. Automation Strategy: Align automation goals with business value and release cycles. Track ROI and continuously optimize coverage. Team Development: Mentor QA engineers, promote best practices, and foster a quality-first mindset. Conduct performance reviews and knowledge-sharing sessions. Process & Governance: Ensure QA process adherence (Agile, DevOps, CI/CD). Perform RCA for production issues and embed learnings. Release Readiness: Lead Go/No-Go decisions based on test coverage and readiness. Ensure environments and test data are in place.

Manager, Quality Assurance Position Overview As a Manager, Quality Assurance Engineer, you be strategic thinker on how to move the QA teams to the next level by investing and investigating on people, process and procedures. You will play a key role in developing the QA teams and helping with QAEs growth of their career pathing, as well as collaborate with stakeholders to identify and improve departmental best practices and processes. Responsibilities and Deliverables Manage team in delivery of test planning, preparation and execution activities. Accountable for all project/release testing of multiple complex initiatives cutting across multiple products. Ensure effective planning and support coordination with stakeholders Oversee creation of testing strategies, plans and project documentation using risk analysis methodologies and tools that align with a project's development approach. Manage documentation creation, review, sign-off (e.g. strategies, plans, schedule, cost estimates, test cases, dashboards, defect logs, test phase closure reports, entry/exit criteria, gating), ensure artifacts adhere to standards and audit requirements. Communicate, address scope changes that may impact testing. Develop, manage operational processes. ensure QA processes tie into technology delivery practices, standards. Counsel IT and business partners, raise awareness. Accountable for team's adherence to processes, timely issue notification, escalated risks and issue reviews, contingency plan development, risk resolution, facilitates overall escalation process. Provide cost/resource estimates and revisions, track financials, provide forecasts as needed. Provide coaching, development, succession, recruitment, resource management, team leadership, input into performance and development plans. Organizational Alignment: Reports to the Director, Quality Assurance Qualifications: Skills & Work Traits Required: Strong work ethic with a positive attitude and a passion for Quality Assurance Strategic thinker looking for a big picture view and understand the impact to the department. Ability to manage multiple testing teams for functions/projects with increasing degree of complexity and broad scope Readiness to work independently and often autonomously in the management of teams and operational disciplines and develop strategic thinking and planning in work plan execution. A continuous learner, with knowledge of current industry-standard automation testing techniques and the drive to share knowledge with your colleagues Positively influences teammates. Respond on feedback with a can do attitude Strong analytical and problem-solving skills Excellent time and risk management skills Excellent interpersonal and communication skills (written and oral), willing to help teammates grow along with their career development Flexible, self-motivated, and comfortable working with multiple teams The ability to work effectively under pressure in a rapidly changing environment to meet deadlines Passionate about understanding our clients Committed to building a high quality, secure, high performing product by building training programs and effectively managing change in these areas Flexible with mode of communication, whether it be with coworkers in-person or online. Able to contribute to an inclusive mindset to promote collaboration.

Implementing & monitoring effective Quality Management System process. QA/QC Documentation including calibration, test results, Evaluation of Source of Raw material. . Required Candidate profile The candidate have to coordinate with sales person importantly handle with existing clints with better deals and search for a new clints for growth of business.

Job Summary: The Medical Coding Quality Analyst Manager is responsible for overseeing the quality and accuracy of medical coding operations. This role ensures compliance with industry standards, payer policies, and regulatory requirements, while also leading quality assurance initiatives, training programs, and process improvements to enhance coding accuracy and efficiency. Key Responsibilities: Quality Assurance & Compliance: Oversee and manage the coding quality review process to ensure compliance with ICD-10-CM, ICD-10 PCS, CPT, HCPCS, and HCC risk adjustment guidelines. Develop and implement auditing processes to monitor coder accuracy and adherence to regulatory and payer requirements. Conduct and oversee internal and external audits to assess coding accuracy and identify areas for improvement. Develop corrective action plans for coders who do not meet accuracy benchmarks. Maintain and analyze coding quality reports, identifying trends and areas requiring training. Training & Development: Provide feedback and coaching to improve coder performance. Collaborate with the Education and Training teams to enhance ongoing learning opportunities. Leadership & Team Management: Supervise a team of quality analysts, auditors, and medical coders. Conduct performance evaluations and provide professional development opportunities. Foster a culture of continuous improvement and compliance. Process Improvement & Documentation: Identify inefficiencies and implement strategies to enhance coding workflow and quality. Maintain detailed documentation of coding audits, quality control measures, and compliance reports. Work cross-functionally with HIM, Compliance, and Revenue Cycle teams to optimize coding accuracy. Stakeholder Collaboration: Serve as a key point of contact for providers, payers, and regulatory agencies on coding-related issues. Assist in the development of policies and procedures to ensure coding integrity. Communicate audit findings and best practices to leadership and stakeholders. Experience: 8+ years of experience in medical coding and auditing. 2+ years of experience in a leadership or managerial role. Strong knowledge of HCC, Risk Adjustment, DRG, CPT, HCPCS, and ICD-10 coding guidelines. Experience with EMR/EHR systems, coding software, and claims processing .

Job Summary: The Medical Coding Quality Analyst Manager is responsible for overseeing the quality and accuracy of medical coding operations. This role ensures compliance with industry standards, payer policies, and regulatory requirements, while also leading quality assurance initiatives, training programs, and process improvements to enhance coding accuracy and efficiency. Key Responsibilities: Quality Assurance & Compliance: Oversee and manage the coding quality review process to ensure compliance with ICD-10-CM, ICD-10 PCS, CPT, HCPCS, and HCC risk adjustment guidelines. Develop and implement auditing processes to monitor coder accuracy and adherence to regulatory and payer requirements. Coding Audits & Performance Monitoring: Conduct and oversee internal and external audits to assess coding accuracy and identify areas for improvement. Develop corrective action plans for coders who do not meet accuracy benchmarks. Maintain and analyze coding quality reports, identifying trends and areas requiring training. Training & Development: Provide feedback and coaching to improve coder performance. Collaborate with the Education and Training teams to enhance ongoing learning opportunities. Leadership & Team Management: Supervise a team of quality analysts, auditors, and medical coders. Conduct performance evaluations and provide professional development opportunities. Foster a culture of continuous improvement and compliance. Process Improvement & Documentation: Identify inefficiencies and implement strategies to enhance coding workflow and quality. Maintain detailed documentation of coding audits, quality control measures, and compliance reports. Work cross-functionally with HIM, Compliance, and Revenue Cycle teams to optimize coding accuracy. Stakeholder Collaboration: Serve as a key point of contact for providers, payers, and regulatory agencies on coding-related issues. Assist in the development of policies and procedures to ensure coding integrity. Communicate audit findings and best practices to leadership and stakeholders. Experience: 8+ years of experience in medical coding and auditing. 2+ years of experience in a leadership or managerial role. Strong knowledge of HCC, Risk Adjustment, DRG, CPT, HCPCS, and ICD-10 coding guidelines. Experience with EMR/EHR systems, coding software, and claims processing .

1. HEAD FINANCE Position: Head Finance Manager Qualification: CA or ICWA Experience: minimum 2-3 years Budget: (As per company standard) Key Responsibilities: 1) Closing of Monthly Financial Accounting with all Schedules. 2) Monthly Financial MIS Preparation 3) Budget Preparation 4) Product Costing 5) Direct Taxation 6) GST Rules and Regulations 7) AR and AP 8) Coordinating with Auditor for yearend audit. 2. MANAGER - QUALITY ASSURANCE FOR QUALITY DEPARTMENT Position: Manager - Quality Assurance Qualification: B.E. / B.Tech. (Mech.) Experience: minimum 8-10 years Budget: (As per company standard) Key Responsibilities: 1) Metallurgical quality of the Final products (castings) delivered to the customers. 2) Process Control of inward receiving materials, core making, molding process, melting process, pouring and knock out. 3) Statistical Quality Control of the processes mentioned in Cl 2. 4) Calibration of Measuring and Testing Equipment. 5) Coordinate for preparing the ISO-9000-2015 and IATF 16949:2016 internal audit plan, schedule. 6) Conducting ISO9000-2015 and IATF 16949: 2016 Internal audit as per schedule. 7) Coordinate the ISO9000-2015 and IATF 16949:2016 Internal audit NC and getting actions, evidence with concerned persons 8) Inspect and certify the quality of incoming raw materials and consumables used for production. 9) Prepare SOP, inspect and ensure Process Parameters for the following. 10) Core sand for core making, coatings and finished cores. 11) Prepared Green sand and molds 12) Molten metal from Induction Melting Furnace 13) Inspect and ensure adherence to process parameters as per Control Plan while pouring and Knock Out. 14) Test the Metallurgical quality of the produced castings from each Batch (Heat) as per Sampling Plan and certify the quality of castings from each Batch. 15) Issue Test Certificate of Materials for each Batch of Finished castings with traceability to heat no and Invoice no. or as per Customer Requirement as the case may be. 16) Liaise with Customers regarding complaints due to Metallurgical deviations and solve the issues. 17) Organize and arrange for timely and periodic calibration of the measuring and test equipment. 18) Maintain record and monitor the calibration status of measuring and test equipment. AUTHORITIES: 19) Take decision on Customer Returned / Rejected Material. 20) Approve Incoming / Final Inspection Reports, Calibration Reports. 21) Stop production and implement corrective action in case of non- compliance of QMS or quality parameters. 22) Improve MIS Data & reference sample 3. JE / SUPERVISOR - PROCESS QUALITY- (QUALITY ASSURANCE Position: JE / Supervisor - Process Quality Qualification: Diploma in Mechanical Engineering or B.E. / B.Tech. (Mech.) Experience: 2 or 3 years in relevant field Budget: (CTC 25 K) Key Responsibilities 1) Receiving Inspection, In process inspection, Final Inspection/Report preparation 2) Approval of deviation which does not affect the customer requirements in consultation 3) Analysis of in-house Quality problem for corrective / preventive action coordination with Production 4) Participating in the Management Review Meeting 5) Preparation of inspection plan / Check list in connection with QC requirements 6) To stop production if there is serious quality problem / take corrective action when non-conformity is noticed / to inform 7) Corrective preventive action with supplier for incoming material quality related issues 8) Calibration of inspection and test measuring equipment. 4. Junior Engineer – Dimensional Accuracy (QA) Position: JE / Supervisor - QA Qualification: Diploma in Mechanical Engineering or B.E. / B.Tech. (Mech.) Experience: 2 or 3 years in relevant field Budget: (CTC 25 K) Key Responsibilities : 1) Dimensional conformance of New pattern equipment and New components. 2) Dimensional conformance of Existing pattern equipment and existing components. 3) Conformance to specification of molding and core making equipment. 4) Defect analysis and defect prevention of internally rejected castings and customer rejected castings. 5) Resolving customer complaints due to dimensional deviation at customer premises. 6) Lay out inspection of a) new pattern equipment b) New castings 7) Periodic inspection of existing pattern equipment as per inspection plan. 8) Periodic Lay Out inspection of current production components as per inspection plan 9) Design and preparation of gauges for Critical dimensional inspection for Final inspection of castings as and when required 10) Periodic inspection of Match plate bushes, mold box bushes, Mold box pins, mold process and core process equipment and inspection gauges for Final inspection 11) Defect analysis of rejected and rework-able castings defect-wise and initiating corrective preventive action to minimize rejections. 12) Defect analysis of rejected/rework-able castings from customers and co-ordinate with QMS personnel to fix the Root cause and initiate CAPA to enable QMS personnel to communicate to customer. 13) Record all corrections/alterations to pattern equipment in Pattern History Card. 14) Use ERP for maintaining data and records related to your job. 5. JE / Supervisor – PPC Key Responsibilities 1) To prepare monthly, weekly and daily production plan for molding, melting and 2) Core shop based on customer requirements. 3) To issue daily production plan, at least 24 hours in advance to the concerned 4) Departments. 5) To monitor the daily production and maintain the stock record of finished goods. 6) To plan monthly material requirement based on BOM and inform purchase 7) Department. 8) To ascertain the availability of cores, chills, sleeves, and other materials required 9) for moldings and core making before issuing the production plan. 10) To prepare MIS reports and inform concerned persons and management. 11) To attend weekly production meeting and maintain minutes of the meeting. 12) Co-ordinate with shop floors line supervisors for ensuring actual daily production Plan. 13) To coordinate with customer regarding production plan and inform customers 14) About daily production of castings. 15) To coordinate with customer regarding customer plan and inform customers 16) About daily dispatch of castings. 17) Co-ordinate with Dispatch team for ensuring the actual daily dispatch planning. 18) Follow outstanding payment from customer. Role & responsibilities

Role & Responsibilities: As a QA Manager , you will lead the Quality function across multiple departments, including Quality Assurance (QA), Quality Control (QC), and Microbiology. This critical role ensures that manufacturing operations are fully compliant with international regulations and consistently meet high-quality standards. You will drive continuous improvement initiatives, manage audits, and oversee the development and implementation of strategies to enhance product quality. Key Responsibilities: Leadership & Quality Culture: Lead, mentor, and inspire the Quality teams, promoting a culture of quality across the organization. Ensure audit readiness at all times and foster a proactive, quality-driven environment. Regulatory Compliance & Audits: Ensure strict adherence to international regulatory requirements such as WHO GHP, Revised Schedule M, and other relevant standards. Manage successful audit outcomes to maintain compliance. Manufacturing Operations: Oversee cGMP-compliant operations, focusing on the production of Oral Solid Dosage (OSD), Small Volume Parenteral (SVP), Beta Lactam, and External Preparations. Manage scale-up processes, new product development, and product lifecycle. SOPs & Documentation: Ensure all Standard Operating Procedures (SOPs) align with WHO GHP, Revised Schedule M, and regulatory guidelines. Work closely with cross-functional teams on new product registrations and updates. Quality Management Systems (QMS) & Continuous Improvement: Strengthen and enhance the QMS across the organization. Drive continuous improvement initiatives, ensuring that quality is maintained and improved at all levels of operation. Risk Management & Compliance: Conduct regular compliance reviews, facilitate facility and equipment qualifications, and manage quality risk assessments to mitigate potential risks to product quality. Dossier Filing for Exports: Oversee and manage the preparation and filing of dossiers for export markets, ensuring that all documentation meets regulatory and quality standards. Key Skills & Experience: Experience in Regulated Environments: Extensive experience in manufacturing environments, particularly in the production of injectable products, with a deep understanding of regulatory standards and compliance processes. Audit & Compliance Management: Strong background in audit management, ensuring successful audit outcomes while maintaining the highest standards of compliance. Leadership & Team Management: Proven leadership ability to manage cross-functional teams, mentor staff, and build a cohesive and effective Quality function. Analytical & Negotiation Skills: Strong analytical skills to assess compliance and quality issues, with the ability to negotiate and resolve challenges effectively. Communication & Collaboration: Excellent verbal and written communication skills, with the ability to collaborate effectively with internal teams and external regulatory bodies. Travel Flexibility: Open to travel up to 50% of the time, managing various scheduling requirements across different sites.

Job Title: QA Manager Department: Quality Assurance Location: Surendernagar, Gujarat. Qualification: M.Pharm / B.Pharm / M.Sc Experience: 8 - 10 years in pharmaceutical QA Reporting To: Head Quality / Plant Head Key Responsibilities: Lead QMS activities: deviations, change control, CAPA, risk assessments, and quality audits. Manage validation activities: process, cleaning, equipment qualification. Review and approve SOPs, BMRs, BPRs, and validation protocols. Handle regulatory inspections and customer audits; ensure effective CAPA implementation. Drive compliance with data integrity and continuous improvement initiatives. Supervise and mentor QA team; collaborate with cross-functional departments. Mandatory Requirements: Must have hands-on exposure to regulatory audits like EU-GMP, MHRA, TGA, and USFDA. Deep understanding of cGMP, quality systems, and global compliance expectations. Skills & Competencies: Strong leadership in quality assurance and regulatory compliance. Excellent communication, documentation, and team management skills. Should Be able to handle the Team .

Position Deputy Manager - Quality Assurance Experience: 7 - 14 Yrs Function: Product & Technology Development Primary Responsibilities: The incumbent will be responsible for the design, implementation, and verification of quality systems across food manufacturing units. Key duties include centralized monitoring of key process and quality performance indicators and reporting through the Management Information System (MIS). The role also involves preparing detailed product trial quality reports and compiling comprehensive documentation (dockets) to facilitate technology transfer to production units. Requirements: Proven knowledge and experience in food quality system design, implementation, and verification. Strong understanding of process control validations in relation to product performance. Familiarity with food safety standards and protocols, including HACCP, ISO, GMP, and related frameworks. Exposure to process automation and quality automation systems is highly desirable. Proficiency in preparing and managing documentation related to quality systems and food safety plans, including procedures and standardized formats. Prior experience in a production environment will be considered an advantage. Competency in using software applications for effective MIS reporting is essential.

Develop and implement QA strategies and systems. Lead and mentor the QA team. Ensure compliance with regulations and standards like ISO. Drive process improvements, manage audits, collaborate with teams, maintain documentation.

Lead Quality function for Forged & machined Auto Components. System / Process Audit. Process improvement ,Supplier Evaluation, IATF, ISO Certification handling. Report to CEO. Required Candidate profile B.E.Mech/ Metallurgy Exp :10-15 Yrs in QA/QC from Auto Components Mfg Cos. for Hot / Cold Forged Components. Supplier Evaluation, IATF, ISO Certification. Prefer Local candidates Tamil speaking Perks and benefits EMAIL CV IN MS WORD WITH SALARY. NO WHATSAAP PLS

JOB DESCRIPTION 1. Formulation & Implementation of project-specify Quality Plan 2. Maintaining Records for Incoming Material Inspection 3. Maintaining Records for Tests on construction materials 4. Records for Labour contractor Evaluation 5. Maintaining Records for Process Control & related inspections, tests 6. Calibration & Validation of Inspection, Measuring & Test Equipment 7. Corrective actions for Non-conformities 8. Inculcation of Quality Awareness in all Engineers 9. Coordination with clients Quality control Engineer 10. Maintaining all Quality records 11. Sample approval and connected Records 12. Document Control for quality plan and site procedures CANDIDATE PROFILE 1. B.Tech/B.E. (Civil)/Dip-Civil with 05 -12 years of experience in QA/QC function 2. Should have exp in QA/QC function from buildings / commercial / IT Parks / Residential projects. 3. Should have sound knowledge of QA/QC procedures right from initial stage to finishing. Interested Candidates may also send their resumes to smita.wadkar@shapoorji.com

Key Responsibilities: - Lead and manage a team of QA engineers, providing mentorship and support. - Develop and implement comprehensive QA strategies and processes. - Collaborate with cross-functional teams to define test objectives and prioritize efforts. - Design, develop, and maintain automated test suites using Java and Selenium. - Conduct code reviews, analyze test results, and optimize test coverage. - Define and track KPIs to measure QA process effectiveness. - Stay current with industry trends and implement relevant tools and techniques. - Establish strong relationships with stakeholders and provide regular updates. - Troubleshoot and resolve complex technical issues. - Foster a culture of quality and collaboration within the QA team. Requirements: Bachelors or Master’s degree in Computer Science, Engineering, or related field. 12-15 years of experience in quality assurance, with at least 5 years in a leadership role. Extensive experience in automation testing using Java and Selenium. Proven track record of managing and mentoring QA teams. Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Experience with Agile/Scrum environments and familiarity with CI/CD pipelines preferred. ISTQB certification and experience with other automation tools (e.g., Cucumber, TestNG) is a plus. Ownership of communicating with the clients and different stakeholders. Ownership of end to end Automation/Manual/Performance Testing activities

*Looking for immediate joiner* Position : SQA Manager Location : Remote Exp :- 7+ Years Required Qualification and Professional Experience: Bachelors or Master’s degree in Computer Science & Engineering or an equivalent degree. 7-10 years experience in manual and automation testing of different domains, mandatorily experienced in SAAS testing on cloud. Experience with web and mobile testing preferred. Should have managed independently the testing strategy of a platform/product. Automation testing with Selenium, Appium etc. will be added advantage. Experience with performance, security, load, stress testing preferred. Sound knowledge on different types of testing, development methodologies and testing life cycle and able to derive maximum test cases for the features under test. Should possess strong knowledge in database like MySQL, MongoDB, ElasticDB. Should have experience in creating test deliverables like test plan, test execution and defect summary report, release notes. Excellent written and verbal communication skills. Experience with Agile development methodologies, JIRA. Responsibilities : Analysing requirements (stories) along with the dev team & identifying test scenarios. Creating detailed, comprehensive and well-structured test plans and test cases. Writing tests based on scenarios identified and creating test data. Executing the tests in multiple environments as per the plan. Writing automation scripts for testing in web, API and mobile automation tools. Exploratory, ad-hoc and negative testing as well as API testing. Using Test Management tools like QC ALM, Jira, Zoho, TestRail etc. Understanding the application framework and architecture of the application and follow through for implementation. Reviewing quality specifications and technical design documents to provide timely and meaningful feedback. Estimating, prioritizing, planning and coordinating quality testing activities. Good understanding of the software testing process (STLC). Good understanding of Test Driven Development (TDD). Good understanding of the business approach (Requirement Understanding & Analysis). Good knowledge of Client-Server Technology and Web Technology. Strong experience in Manual testing by handling all Test Life Cycle activities. Good practice of Quality process standards and Strategies. Understand the functions, interactions and dependencies among components within the application. Knowledge on performance tools like JMeter, Neo Load, Load Runner. Exposure on API tools like Soap UI, Postman, Rest. Strong experience in defect management and able to participate in bug triages. Implements work-plans and schedules as assigned. Seeks assistance when needed, demonstrates self-initiative. Sphere of influence primarily limited to immediate work group. Mandatory to possess clear communication skills, outspoken, sharp business focus, collaborative nature.

The Associate General Manager – Operations will lead end-to-end supply chain, inventory, and production operations Purchase, Inventory, Warehouse & Logistics cross-functionally work with R&D, BD & Mktg, Accounts & Finance/ external partners Required Candidate profile New Product Development Purchasing & Procurement Production Mgmt QA,supply chain alignment Departmental Oversight & Functionality Strategic Leadership & Reporting

Job Title: QA Manager Department: Quality Assurance Location: Surendernagar, Gujarat. Qualification: M.Pharm / B.Pharm / M.Sc Experience: 8 - 10 years in pharmaceutical QA Reporting To: Head Quality / Plant Head Key Responsibilities: Lead QMS activities: deviations, change control, CAPA, risk assessments, and quality audits. Manage validation activities: process, cleaning, equipment qualification. Review and approve SOPs, BMRs, BPRs, and validation protocols. Handle regulatory inspections and customer audits; ensure effective CAPA implementation. Drive compliance with data integrity and continuous improvement initiatives. Supervise and mentor QA team; collaborate with cross-functional departments. Mandatory Requirements: Must have hands-on exposure to regulatory audits like EU-GMP, MHRA, TGA, and USFDA. Deep understanding of cGMP, quality systems, and global compliance expectations. Skills & Competencies: Strong leadership in quality assurance and regulatory compliance. Excellent communication, documentation, and team management skills. Should Be able to handle the Team .

JOB DESCRIPTION 1. Formulation & Implementation of project-specify Quality Plan 2. Maintaining Records for Incoming Material Inspection 3. Maintaining Records for Tests on construction materials 4. Records for Labour contractor Evaluation 5. Maintaining Records for Process Control & related inspections, tests 6. Calibration & Validation of Inspection, Measuring & Test Equipment 7. Corrective actions for Non-conformities 8. Inculcation of Quality Awareness in all Engineers 9. Coordination with clients Quality control Engineer 10. Maintaining all Quality records 11. Sample approval and connected Records 12. Document Control for quality plan and site procedures CANDIDATE PROFILE 1. B.Tech/B.E. (Civil)/Dip-Civil with 05 -12 years of experience in QA/QC function 2. Should have exp in QA/QC function from buildings / commercial / IT Parks / Residential projects. 3. Should have sound knowledge of QA/QC procedures right from initial stage to finishing. Interested Candidates may send their resumes to ban.hrd@shapoorji.com

Role Overview As QA Project Lead, you manage the QA plan for a game title or major service/feature. You will be involved in functional test planning, execution, and reporting on the project under management. You will be involved in process improvement plans and improve on level of quality. You will also be the user of data and Indicators and bring it into practice. Responsibilities • Manage the planning, execution, and reporting processes of QA team. • Complete testing for projects and comprehensive bug tracking and reporting. • Measure on quality assurance metrics. Use metrics to anticipate issues affecting the health or quality of the game, and to some extent, the team. • Work on day-to-day tasks and actively engaged with team members; quickly voice concerns or issues that need to be addressed. • Monitors the use of existing processes and provide feedback on areas of improvement. Participate in process optimization tasks as directed by the manager. • Identify risks and take necessary actions to address them or raise concerns to the management team. • Work with other teams (Game Development, Compliance, Certification) and the project owner to ensure the teams are working as efficiently as possible. • Help in monitoring team members performance. • Help manage the capacity plan; scheduling and tracking; and change requests. • Communicate issues, concerns, and successes to partners. Have Experience • 5+ years of experience in Quality Assurance including 1 or more years in leading a project. 1+ years of experience in people management. • Experience with project management and bug tracking tools (e.g. Jira) in an agile environment. • Game development experience especially full cycle experience on shipped titles and familiarity with FPS game are plus. • Experience as a vendor or outsourcing manager over-seeing a AAA game/s through the full development cycle, from concept to live service is a plus

Role & responsibilities Hands-on experience in managing Quality Assurance activities in Manufacturing Sheet Metal / Other Fabricated products. To Develop and implement quality control plans, procedures, and standards for Sheet metal fabricated products esp. for the Electrical Industry. Handling a team of Engineers and Responsible for quality assurance at all stages viz., Inward, In-process & Final inspection and testing of the products. To handle customer complaints and identify areas of improvement and implement corrective actions. Responsible for Monitoring and controlling all the process parameters to be maintained to get good quality product. To have Strong knowledge in ISO 9001:2015 requirements and responsible for quality management system (QMS) compliance across all departments. To Handle Internal & External ISO Audits, Customer audits and other Product Test & certifications. candidate must have In depth knowledge in Analysis of Quality parameters and SPC tools. To Collaborate with cross-functional teams to resolve quality issues and improve product and process reliability. To Provide training on QMS principles, tools, and best practices to employees at all levels. Preferred candidate profile Candidate with 8-13 years of experience in QA Management and a B.Tech/B.E. degree in Electrical or Mechanical stream is preferred. Candidate having experience in Paint / Powder coating Quality assurance is added advantage. Candidate having exposure on Enclosure IP/NEMA testing and UL certification will be an added advantage.

Perform maintenance of company SOPs in compliance with ICH-GCP, international and national regulations Review, approval and archival of company SOPs in compliance with ICH-GCP, international and national regulations Review and maintain company archives of clinical protocols and study documents Conduct QA internal audits of all aspects of the Clinical Research Departments activities to ensure compliance with ICH-GCP and applicable international and company procedures Perform QA reviews of protocols and other documents and data in preparation for submission to IRB/IEC, regulatory health authorities and publications Provide training to research staff on GCP, ICH and local regulations (as required) Generate, maintain and manage documents and training records of the activities of the Clinical Research Department Document Control & Issuance Preparation of Master Index to all QAU files & Documents Filling of all Master documents after approval in a sequential way so that it can be easily identified Skills and Knowledge needed on the following guidelines ICH-GCP ISO9001:2015 ISO14155:2011 ISO13485:2016

Department: Quality Assurance Role Overview: The Quality Assurance (QA) Manager will oversee all aspects of quality assurance within the electronic or electrical assembling unit. This includes developing and implementing quality management systems, ensuring compliance with industry standards and regulations, and leading a team of quality professionals. The QA Manager will work closely with production, R&D,engineering and supply chain teams tmaintain high-quality standards and drive continuous improvement initiatives. Role & Responsibilities: 1. Quality Management System (QMS): Develop, implement, and maintain the Quality Management System (QMS) in compliance with industry standards such as IS9001, IPC-A-610, IATF or similar. Ensure all quality processes, procedures, and documentation are up tdate and effectively communicated across the organization. Monitor and evaluate quality assurance processes across all functional areas tensure adherence tindustry standards and client requirements. Conduct regular audits and reviews tassess the quality and effectiveness of deliverables and processes. 2. Compliance and Audits: Ensure compliance with all applicable regulations, standards, and customer requirements. Prepare for and lead internal and external audits, including those by regulatory bodies, customers, and certification organizations. 3. Inspection and Testing: Oversee the inspection and testing of raw materials, in-process products, and finished goods tensure they meet established quality standards. Develop and implement inspection protocols, sampling plans, and testing procedures. 4. Root Cause Analysis and Corrective Actions: Investigate quality issues, identify root causes, and implement corrective and preventive actions (CAPA). Monitor the effectiveness of CAPAs and adjust processes as needed tprevent recurrence. 5. Supplier Quality Management: Collaborate with the supply chain/Purchase team tevaluate and approve suppliers based on quality criteria. Conduct supplier audits and assessments tensure compliance with quality standards. 6. Continuous Improvement: Lead continuous improvement initiatives tenhance product quality, reduce waste, and improve overall efficiency. Implement lean manufacturing principles and Six Sigma methodologies where applicable. 7. Team Leadership: Manage and develop the QA team, including hiring, training, and performance management. Foster a culture of quality, accountability, and continuous improvement within the team. 8. Customer Interface: Serve as the primary point of contact for customer quality-related inquiries and concerns. Collaborate with customers tunderstand their quality expectations and ensure satisfaction. 9. Reporting and Documentation: Prepare regular reports on quality performance, including key metrics such as defect rates, audit results, and customer feedback. Maintain accurate and organized records of all quality activities and documentation. Qualifications: Bachelors degree in Engineering, Quality Management, or a related field. Minimum of 10 years of experience in quality assurance, preferably in the electronics/electrical manufacturing industry. Candidate MUST have experience working in tier 1 autcomponent OEM companies like Schneider, Schaeffler etc in Electrical/Electronic related fields. Strong knowledge of industry standards such as IS9001, IPC-A-610, IATF and other relevant regulations. Experience with quality management systems (QMS) implementation and maintenance. Strong leadership and interpersonal skills, with the ability tmotivate and lead cross functional teams Excellent problem-solving and analytical skills, with the ability tidentify and resolve quality issues Excellent verbal and written communication skills, with the ability tpresent complex information tstakeholders at all levels Certification in Six Sigma, Lean Manufacturing, or similar quality-related programs is a plus

Experience: 16+ yrs in purely technical leadership (no managerial experience to be considered), in QE large part of that must be in automation Strong domain SNVC skills. Strong test automation background and skills; Python + Java is preferred; however at least Python is must have. Automation experience must cover framework design/development, creating test strategies and handling frequent changes in test requirement Excellent QE aptitude and experience in providing technical leadership to medium to large teams. Experience working in Agile environment Excellent communication skills (verbal and written both)