Job Description

Key Responsibilities:

Lead and manage QC operations for raw materials, in-process, and finished products.

Oversee analytical testing methods: HPLC, UV Spectrophotometer, Kjeldahl, KF Titrator, SDS-PAGE, Hydroxyproline test, Protein content analysis.

Review and approve COAs, protocols, and reports in compliance with GMP, ISO 13485, and 21 CFR Part 11.

Ensure calibration and preventive maintenance of QC instruments.

Train and mentor QC team to maintain accuracy, compliance, and data integrity.

Handle deviations, OOS/OOT investigations, and implement CAPA.

Ensure audit readiness and regulatory compliance at all times.

Prepare, review, and control QC documents (SOPs, protocols, reports, records).

Approve test protocols and reports; ensure proper record keeping.

Plan and utilize manpower, equipment, and consumables effectively.

Oversee method validation, verification, and transfer for chemical and microbiological tests.

Qualifications & Experience:

M.Sc. (Chemistry / Biochemistry) or B.Pharm / M.Pharm.

5-8 years of QC experience in pharmaceuticals / medical devices / biotech,

Strong knowledge of analytical techniques and regulatory requirements.

Experience in handling customer and regulatory audits preferred.

Job Type: Full-time

Pay: From ?35,000.00 per month

Benefits:

Paid sick time Paid time off
Experience:

hr: 2 years (Preferred) HR sourcing: 1 year (Required)
Language:

English (Required)
Work Location: In person