Sample Collection & Testing: Collect and test raw materials, packaging components, in-process samples, finished products, and stability samples, following SOPs.
Instrumental Analysis: Perform chemical and physical analyses using HPLC, UV, FTIR, GC, etc.
Documentation & Reporting: Maintain accurate records, logbooks, and prepare Certificates of Analysis (CoA) as per Good Documentation Practices (GDP).
Stability & In‑Process Checks: Conduct stability studies and perform in-process quality checks during production.
Equipment Management: Ensure calibration and preventive maintenance of QC instruments; report malfunctions promptly.
Compliance & Audits: Adhere to GMP, cGMP, ICH, and regulatory standards; support internal and external audits, and assist with investigations, deviations, OOS handling, and CAPA implementation.
Qualifications & Skills
Educational Qualification: B.Pharm, M.Pharm, B.Sc/M.Sc in Chemistry or related field as applicable.
Experience: Typically ranging from 1 to 3 years in pharmaceutical quality control roles.
Technical Proficiency: Hands on experience with HPLC, UV, GC, FTIR, along with strong understanding of GMP, GLP, and data integrity practices.
Attention to Detail: Excellent accuracy in testing, documentation, and adherence to protocols.
Analytical Mindset: Capable of troubleshooting and identifying root causes for quality incidents.
Soft Skills: Strong communication, teamwork, and ability to work effectively under audit-ready environments.
Benefits & Work Conditions
Job Type: Full-time, Permanent; typically morning/day shift.
Salary Range: Approximately ₹25,000 to ₹30,000 per month (depending on role level and experience).
Perks: Provident Fund, Paid Sick Time, Cell Phone Reimbursement, Health Insurance.