- Testing of all laboratory samples including raw materials, in-process, finished products,
- To carry out Validation, stability study of finished product (as per written procedure or as per pharmacopoeia).
- Ensuring all cGMP/GLP requirements are strictly adhered to and that SOP’s are always followed
- Recording of analytical results accurately.
- Operation, maintenance and calibration of laboratory instruments like pH meter, balances, Dissolution
- Maintaining usage of laboratory chemicals and keeping records.
- Ensuring that the laboratory is kept clean, tidy and safe at all times.
- Report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior.
- Verify analytical data and carryout documentation as required
- Participate in internal audits of GMP.
- Ensuring training record is kept up to date.
- Maintaining the good documentation in the quality control department
- Reporting of Out of specification, Deviation and incidents in the laboratory to manager.
- Support in daily routine analysis and adhere to GMP at all times.
- Handling of samples as per procedure
- Knowledge of Microsoft word and Excel
- Preparation of SOPs and Operating instructions
- Hands on HPLC, UV, IR and Dissolution is must
Job Types: Full-time, Part-time
Experience:
Work Location: In person
