Key Responsibilities
- Monitor Cleanrooms: Inspect controlled manufacturing environments to ensure strict sterile protocols are followed. [1]
- Perform Assays: Execute chemical, biological, and physical testing on raw materials, in-process batches, and finished drug products. [1, 2]
- Audit Documentation: Review batch records, laboratory logs, and sterilization records for absolute accuracy.
- Follow Compliance: Enforce strict adherence to Current Good Manufacturing Practices (cGMP), FDA regulations, and standard operating procedures (SOPs).
- Calibrate Equipment: Maintain and calibrate sensitive laboratory instruments such as High-Performance Liquid Chromatography (HPLC) systems, pH meters, and autoclaves.
- Investigate Deviations: Document out-of-specification (OOS) results and participate in root-cause investigations.
Job Requirements
- Education: 12th Pass , ITI , Chemistry, Biochemistry,
- Experience: 1 to 2 years of QC laboratory experience within a regulated pharmaceutical or biotech manufacturing environment.
- Technical Skills: Strong understanding of cGMP, aseptic techniques, microbial testing, and laboratory safety protocols.
- Soft Skills: Exceptional attention to detail, strong analytical thinking, and precise technical writing skills.
Pay: ₹15,000.00 - ₹18,000.00 per month
Work Location: In person
