Quality Control In-charge

Key Responsibilities & Duties

• Laboratory Operations Management:
• Oversee daily testing schedules for raw materials, packaging materials, in-process samples, and finished products.
• Ensure compliance with cGMP (Current Good Manufacturing Practices) and GLP (Good Laboratory Practices) inside the lab.
• Testing & Validation:
• Review and approve analytical test data, chromatograms (HPLC/GC), and Certificates of Analysis (CoA).
• Supervise method validations, instrument calibrations, and analyst qualifications.
• Investigations & Compliance:
• Investigate OOS (Out-of-Specification) and OOT (Out-of-Trend) results, deviations, and laboratory incidents.
• Implement CAPA (Corrective and Preventive Action) plans for identified lab issues.
• Audit Readiness:
• Maintain audit-ready lab documentation, logbooks, and Standard Operating Procedures (SOPs).
• Face regulatory inspections (e.g., USFDA, MHRA, CDSCO) for the QC domain.

Required Qualifications & Skills

• Education:
• Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm) or Post-Graduation in Chemistry (M.Sc).
• Experience:
• Minimum 5 to 8 years of pharmaceutical QC experience, with at least 2–3 years in a supervisory or in-charge role.
• Technical Skills:
• Hands-on expertise with advanced analytical instruments like HPLC, GC, UV-Spectrophotometer, and dissolution apparatus.
• Strong knowledge of pharmacopeial standards (IP, USP, BP).
• Core Competencies:
• People management, data integrity awareness (ALCOA+ principles), problem-solving, and cross-functional coordination with Production and Quality Assurance (QA).

Pay: ₹8,838.73 - ₹46,451.57 per month

Work Location: In person