Position: QC Head / Approved Chemist

We are looking for an FDA-approved/authorized Chemist with a minimum of 7 years’ experience in a WHO-GMP pharmaceutical manufacturing unit.

Key Responsibilities:

- Manage and supervise all day-to-day Quality Control (QC) activities.
- Perform and review testing of Raw Materials, Packaging Materials, In-process Samples and Finished Products.
- Operate and handle laboratory instruments including HPLC, UV-Visible Spectrophotometer, Gas Chromatography (GC) and other QC testing equipment.
- Conduct testing as per applicable IP, BP and other approved pharmacopoeial standards/specifications.
- Ensure proper documentation, SOP compliance, laboratory records and data integrity.
- Handle method validation, analytical procedures,



calibration and qualification of QC instruments.
- Ensure compliance with WHO-GMP, Schedule M and applicable FDA/Drug Control requirements.
- Lead the QC team and ensure timely completion of all testing and reporting activities.
- Coordinate with Production, QA and regulatory authorities during inspections and audits.

Experience: Minimum 7 years in pharmaceutical QC, preferably with hands-on experience in a WHO-GMP compliant unit. Essential: Valid eligibility/approval as Chemist from the concerned Drug Control/FDA authority.

Pay: Up to ₹500,000.00 per year

Work Location: In person

📌 QC Chemist (Siltara)
🏢 OPG Pharma
📍 Siltara