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
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
About Tecknotrove Systems Tecknotrove Systems is fast growing technology company headquartered in Mumbai. Tecknotrove is Asias leading developer and manufacturer training testing and research on critical applications in industries like Automotive, Aviation, Mining and construction, Defence,
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
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
Quality Specialist (QS)Location Becharaji - Gujarat, India FORVIA HELLA is a listed international automotive supplier. As a company of the FORVIA Group, FORVIA HELLA stands for high-performance lighting technology and vehicle electronics and, with the Lifecycle
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
Description: Manage User Access Management (UAM) activities for Production Shop Floor GxP applications, including user provisioning, modification, deactivation, periodic access reviews, and compliance with regulatory requirements. Handle IT-related QMS activities such as Deviation, CAPA, Change Control, Incident Management,
Thorough study and review of project drawings, BOQ, contract specifications, and quality requirements. Responsible for the effective implementation, maintenance, and continual improvement of AELs Quality Management System (QMS) to ensure compliance with organizational, contractual, and regulatory requirements.
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical
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
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
Lead and maintain the Pharmaceutical Quality System (PQS) by establishing, implementing, monitoring, and continuously improving quality systems in compliance with ICH Q7, ICH Q9(R1), ICH Q10, applicable cGMP regulations, and company quality policies to ensure a
About the Company Ajanta Pharma is a specialty pharmaceutical company committed to developing, manufacturing, and marketing high-quality, affordable medicines. Headquartered in Mumbai, India, the company has a strong presence across India and international markets, with operations
Were Hiring | Quality Assurance Professionals (IVD Industry) Position: Officer / Executive / Assistant Manager – Quality Assurance (IVD) Location: Vapi, Gujarat Company: Meril Diagnostic Pvt. Ltd. Are you passionate about driving quality excellence in the