Assistant/Deputy Manager – Production

Pon Pure Chemicals Group; Bavla; On-site; INR 700,000 - 950,000; Full time

Job summary

Pon Pure Chemicals Group is seeking an experienced professional in production validation with a Gujarat FDA approved certification. You will review BMR/BPR, ensure GMP compliance, verify materials, coordinate with QC, and manage validation activities in a pharma manufacturing setting.

Applicants should hold an MSc/BSc in Chemistry or B.Pharm/B.Tech Chemical Engineering with 4–5 years of API/bulk drugs experience. Strong documentation and analytical skills, plus good teamwork, are essential.

Qualifications

• M.Sc./B.Sc. in Chemistry is required.
• B.Pharm or B.Tech in Chemical Engineering is required.
• Gujarat State FDA approved technical person in production certification is mandatory.
• Minimum 4–5 years of API/Bulk Drugs/pharmaceutical manufacturing industry experience.

Responsibilities

• Review and endorse Batch Manufacturing Records (BMR) & Batch Packing Records (BPR).
• Ensure compliance with GMP and regulatory requirements.
• Verify raw materials, in-process materials & finished goods as per specifications.
• Coordinate with QC for testing and product approvals.
• Monitor critical process parameters and validated processes.
• Execute validation protocols and reports (IQ, OQ, PQ).
• Maintain Validation Master Plan (VMP) and revalidation schedules.
• Develop and review SOPs related to validation activities.
• Ensure documentation compliance and data integrity.
• Support internal, customer & regulatory audits.
• Ensure safety, hygiene & environmental compliance.
• Strong knowledge of GMP & regulatory requirements.
• Good documentation & analytical skills.
• Strong problem-solving and decision-making ability.
• Effective communication & teamwork skills.

Education

M.S.C. in Chemistry

B.S.C. in Chemistry

B.Pharm / B.Tech Chemical Engineering

Gujarat State FDA Approved Technical Person in Production Certification

Job description

Qualifications

Gujarat State FDA Approved Technical Person in Production Certification is mandatory

• M.Sc. / B.Sc. in Chemistry


• B.Pharm / B.Tech Chemical Engineering


• Minimum 4–5 years of experience in API/Bulk Drugs/ Pharmaceutical Manufacturing Industry

Salary:

As per industry norms

Responsibilities

• Review and endorse Batch Manufacturing Records (BMR) & Batch Packing Records (BPR)


• Ensure compliance with Good Manufacturing Practices (GMP)


• Verify raw materials, in-process materials & finished goods as per specifications


• Coordinate with QC for testing and product approvals


• Monitor critical process parameters and validated processes


• Execute validation protocols and reports (IQ, OQ, PQ)


• Maintain Validation Master Plan (VMP) and revalidation schedules


• Develop and review SOPs related to validation activities


• Ensure documentation compliance and data integrity


• Support internal, customer & regulatory audits


• Ensure safety, hygiene & environmental compliance


• Strong knowledge of GMP & regulatory requirements


• Good documentation & analytical skills


• Strong problem-solving and decision-making ability


• Effective communication & teamwork skills