- Quality Control & Testing: Analyze raw materials, packaging materials, and finished bulk drugs as per pharmacopeial standards Perform in-process monitoring, stability testing, and sterility/microbiological testing
- Compliance & Documentation: Maintain cGMP, GLP, and WHO-GMP standards within the manufacturing or laboratory facility Prepare and audit reference standards, batch records, Certificate of Analysis (COA), and Standard Operating Procedures (SOP)
- Instrument Calibration & Method Development: Calibrate and troubleshoot analytical instruments,Ensure compliance with FDA, GMP, ISO, and other applicable regulatory requirements.
- Internal Audits & Co-ordination:Manage readiness for customer, FDA, GMP, ISO, and third-party audits.Conduct internal audits, CAPA implementation, and quality improvements.Collaborate with Production, QA, Regulatory, and R&D teams.
Pay: ₹20,000.00 - ₹35,000.00 per month
Benefits:
- Flexible schedule
- Leave encashment
- Paid time off
- Provident Fund
Ability to commute/relocate:
- Thane, Maharashtra (Thane, Thane District): Reliably commute or planning to relocate before starting work (Preferred)
Application Question(s):
- Are you a FDA approved Chemist
Education:
Experience:
License/Certification:
Work Location: In person
