Assist in batch manufacturing processes such as granulation, compression, coating, filling, and packing under supervision.
Follow Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs).
Ensure cleanroom hygiene, gowning practices, and compliance with GMP norms.
Support in equipment cleaning and line clearance activities as per protocol.
Learn basic operation of production equipment and understand process flow.
Quality (QA/QC) Support:
Assist in sampling and testing of raw materials, in-process materials, and finished products (under guidance).
Support in review and preparation of documentation such as BMRs, logbooks, deviation reports, etc.
Learn and follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
Participate in calibration, equipment qualification, and validation processes.
Compliance & Documentation:
Ensure proper documentation of records, logs, and reports as per regulatory and company standards.
Support audit preparation and compliance with USFDA, WHO, MHRA, and other regulatory guidelines.
Required Skills
Basic understanding of pharmaceutical manufacturing and quality systems
Knowledge of GMP, GLP, and ICH guidelines
Good observation, communication, and documentation skills
Willingness to work in a regulated, team-based environment
Basic computer skills (MS Word, Excel)
Required Qualification:- B.Pharm/M.Pharm Salary :- Upto 2.00 LPA If you are interested for this opening please send updated resume on cv@qualityhr.co.in or revert on same mail with following details. Total No. of Years Experience :- Current CTC :- Expected CTC :- Notice Period :-