Description: Independently conduct and prepare investigation reports for Product Quality Complaints, Unplanned Deviations, OOS, OOT, and OOAL events, ensuring timely closure and regulatory compliance. Perform root cause analysis using appropriate tools (5-Why, Fishbone, Risk Assessment, etc.) and
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Description Senior Specialist, Veeva QMS Technical Product Management The Opportunity Based in Hyderabad, join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity, forward momentum, and
Description: Managing overall activity of QMS. Establishing and implementing quality systems to comply cGMP. Handling of Product Complaint, Deviation, OOS (Out of Specification), OOT (Out of Trend), Incident and Change Control. CAPA management, tracking, verification of implemented CAPA
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The main missions of the role are: Perform engineering assignments as part of design /
Department- LAPS Development Company- Novo Nordisk Global Business Services (GBS) Lead the end-to-end delivery of a mission-critical laboratory platform that touches every corner of our global QC and R&ED operations – and ultimately, the patients who
Description: Faurecia clean mobility is looking for a Design Engineer for its Engineering Unit at Pune. The main missions of the role: Follow the work instructions and work descriptions given by the product design leader Follow
Key Responsibilities: 1. CSV Strategy & Governance - Develop and maintain the overall CSV strategy and validation master plans for global systems. - Ensure compliance with GAMP 5, USFDA, EU Annex 11, 21 CFR Part 11,
Drive and coordinate Quality Control activities for Incoming Inspection are to ensure zero shop complaints and to improve in overall inspection processes. Your Role: Knowledge about basic EHS guidelines/Environmental aspect and Risk related to inspection activities
Role: QA Lead – IT Operations (IT QC SME) Location: Hyderabad Summary The IT QA Subject Matter Expert (SME) will serve as the primary expert and point of contact for quality‑related computerized systems, including Veeva DMS,
About Business: Adani Group: Adani Group is a diversified organisation in India comprising 10 publicly traded companies. It has created a world-class logistics and utility infrastructure portfolio that has a pan-India presence. Adani Group is headquartered
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismDeals Management LevelSenior Associate Job Description & SummaryAt PwC, our people in audit and assurance focus on providing independent and objective assessments of financial statements, internal controls, and other assurable information
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismDeals Management LevelAssociate Job Description & SummaryAt PwC, our people in audit and assurance focus on providing independent and objective assessments of financial statements, internal controls, and other assurable information enhancing
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Description: The position provides enterprise leadership for Quality Assurance (QA) governance, regulatory compliance, and Quality Management Systems (QMS) across pharmaceutical manufacturing operations, including combination products in alignment with applicable global regulations and standards. The role defines, implements,
Key Responsibilities To prepare and review of URS, DQ, QRM, FAT, SAT, and vendor/ supplier’s documents related to qualification. To execute Qualification / Re-Qualification and Validation activities of Equipment / System / Facility and Plant utilities
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismRisk Management LevelAssociate Job Description & SummaryAt PwC, our people in audit and assurance focus on providing independent and objective assessments of financial statements, internal controls, and other assurable information enhancing