Key Responsibilities of the CQA Executive Candidate should have atleast 6 to 8 years experience in QA or CQA department in Pharma segment only Ensures adherence to global regulatory standards such as GMP, ISO, and FDA guidelines. Should have knowledge of All SOP preparation in CQA Department Monitors changes in regulations and updates company policies accordingly. Quality Audits: For internal and Vendor audits too Conducts regular internal audits to assess compliance with quality standards. Prepares for and facilitates external audits by regulatory agencies. Risk Management: Identifies potential risks in processes and implements strategies to mitigate them. Conducts root cause analysis and implements corrective and preventive actions (CAPA). QMS Activity handdling :- candidate should have whole QMS knowledge Qualification & Experience B. Pharma/ M. Pharma / M.Sc. /B.sc Experience range - 6 - 8 years Candidates with Prior experience in CQA are invited. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Key Responsibilities of the CQA Executive Candidate should have atleast 6 to 8 years experience in QA or CQA department in Pharma segment only Ensures adherence to global regulatory standards such as GMP, ISO, and FDA guidelines. Should have knowledge of All SOP preparation in CQA Department Monitors changes in regulations and updates company policies accordingly. Quality Audits: For internal and Vendor audits too Conducts regular internal audits to assess compliance with quality standards. Prepares for and facilitates external audits by regulatory agencies. Risk Management: Identifies potential risks in processes and implements strategies to mitigate them. Conducts root cause analysis and implements corrective and preventive actions (CAPA). QMS Activity handdling :- candidate should have whole QMS knowledge Qualification & Experience B. Pharma/ M. Pharma / M.Sc. /B.sc Experience range - 6 - 8 years Candidates with Prior experience in CQA are invited. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Key Responsibilities :- Male Candidate Required From Maharashtra Location Strategy & Systems: Develop and implement quality systems (QMS) aligned with GMP, GLP, and regulatory norms (FDA, CDSCO). Leadership: Lead, train, and mentor QA/QC teams, setting department objectives and managing budgets. Operations Oversight: Supervise testing of raw materials, in-process, and finished products; manage documentation, validations, and change controls. Compliance & Audits: Ensure adherence to regulations, prepare for audits, and manage internal/external inspection readiness. Problem Solving: Investigate quality issues, implement Corrective & Preventive Actions (CAPAs), and drive continuous improvement. Cross-functional Collaboration: Work with R&D, Production, and Regulatory teams to integrate quality into all processes. Reporting: Prepare quality reports and present quality performance to senior management. Revised schedule M :- Need to implement inline in factory departments within 1 year Smart and excellent skill person required who tackle all difficult situations Essential Skills & Qualifications Education: B.Pharm/M.Pharm, Life Sciences/M.Sc. B.Sc.Chemistry background. Experience: 17 to 20 years of experience Technical: Deep knowledge of GMP, GLP, validation, analytical techniques (HPLC, GC). Soft Skills: Strong leadership, problem-solving, analytical, communication, and attention to detail. Job Types: Full-time, Permanent Pay: ₹1,400,000.00 - ₹1,600,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Work Location: In person
Key Responsibilities :- Male Candidate Required From Maharashtra Location Strategy & Systems: Develop and implement quality systems (QMS) aligned with GMP, GLP, and regulatory norms (FDA, CDSCO). Leadership: Lead, train, and mentor QA/QC teams, setting department objectives and managing budgets. Operations Oversight: Supervise testing of raw materials, in-process, and finished products; manage documentation, validations, and change controls. Compliance & Audits: Ensure adherence to regulations, prepare for audits, and manage internal/external inspection readiness. Problem Solving: Investigate quality issues, implement Corrective & Preventive Actions (CAPAs), and drive continuous improvement. Cross-functional Collaboration: Work with R&D, Production, and Regulatory teams to integrate quality into all processes. Reporting: Prepare quality reports and present quality performance to senior management. Revised schedule M :- Need to implement inline in factory departments within 1 year Smart and excellent skill person required who tackle all difficult situations Essential Skills & Qualifications Education: B.Pharm/M.Pharm, Life Sciences/M.Sc. B.Sc.Chemistry background. Experience: 17 to 20 years of experience Technical: Deep knowledge of GMP, GLP, validation, analytical techniques (HPLC, GC). Soft Skills: Strong leadership, problem-solving, analytical, communication, and attention to detail. Job Types: Full-time, Permanent Pay: ₹1,400,000.00 - ₹1,600,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Work Location: In person