Quality Assurance (Pharmacy)

Roles & Responsibilities

• Review and approval of MBR, APQR, and QA documentation
• Handle deviations, change control, CAPA, complaints, and QMS activities
• Execute and review media fill studies, process simulations, and equipment qualification
• Ensure cGMP and regulatory compliance (USFDA, EU, CDSCO)
• Coordinate with cross-functional teams for compliance and audit readiness
• Use QA systems such as Trackwise, SAP, LIMS, DMS, and Minitab

Available Positions

• QA – Documentation (Team Leader / Manager)
Qualification: B.Pharm / M.Pharm
Experience: 10–13 years

• QA – QMS (Executive / Sr. Executive)
Qualification: B.Pharm / M.Pharm
Experience: 3–7 years

• QA – Media Fill / Validation (Asst. Manager)
Qualification: B.Pharm / M.Pharm
Experience: 8–10 years

• QA – Media Fill / Validation (Executive / Sr. Executive)
Qualification: B.Pharm / M.Pharm
Experience: 3–7 years

Skills

• Sterile QA operations
• QMS (Deviation, CAPA, Change Control)
• Media fill & validation activities
• Regulatory compliance
• Documentation & audit handling

About the Organization

Micro Labs Limited is a reputed Indian pharmaceutical company with strong expertise in sterile manufacturing and global regulatory compliance, offering stable growth and exposure to advanced quality systems.