The Quality Control Chemist is responsible for ensuring that all raw materials, in-process materials, finished products, purified water, packaging materials, and environmental samples meet the required quality standards and regulatory requirements. The role involves performing analytical testing, operating laboratory instruments, maintaining GMP-compliant documentation, supporting investigations, and ensuring compliance, GMP and applicable medical device and pharmaceutical regulations. Perform sampling and analysis of raw materials, chemicals, salts, excipients, and packaging materials.

- Verify compliance with approved specifications and pharmacopeial standards (IP, USP, BP, EP where applicable).
- Release or reject raw materials based on analytical results.
- Conduct routine in-process testing during manufacturing.




- Monitor critical quality parameters of dialysis concentrates and consumables.
- Coordinate with Production to ensure process compliance and product quality.
- Perform testing of finished dialysis consumables before batch release.
- Ensure compliance with approved specifications Qualification • B.Sc./M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or a related science discipline.

Experience 0-1 years of Quality Control experience in pharmaceutical manufacturing.

Required Skills • Robust knowledge of GMP, GLP, GDP, and laboratory safety • Familiarity with ISO 13485 requirements for medical devices.

- Documentation accuracy • Time management • Having good knowledge of Laboratory Instrument Operation

📌 Assistant Quality Chemist (Pune)
🏢 PS Human Resources and Consultants
📍 Pune