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Biotech QA Analyst/Executive Jobs, Softgel Healthcare Jobs
Professionals looking for stable and rewarding roles in pharmaceutical quality systems will find the latest update on Biotech QA Analyst/Executive Jobs, Softgel Healthcare Jobs especially valuable. These opportunities are ideal for candidates aiming to build a strong career in QA within the biotech and nutraceutical manufacturing sector, offering hands-on exposure to GMP compliance, documentation, and quality processes.
Soft gel Healthcare private limited
Company name: Soft Gel Healthcare Private Limited (Chennai)
Job Role: Quality Control Analyst / QC Executive
Salary Range : ₹4.0 LPA to ₹6.0 LPA
Location: Chennai (On-site)
Company: Soft Gel Healthcare Private Limited
Experience Required: Minimum 3 years in QC / Life-sciences / Pharma environment
Employment Type: Full time (shifts / day shift depending on production needs)
Application Mode: Walk-in Interview
Key Responsibilities
• Perform routine and non-routine analytical tests (chemical, physical, microbiological — depending on product line) on raw materials, in-process samples, finished products, packaging materials etc.
• Perform and document instrument calibrations, validation checks, and maintenance logs of QC instruments.
• Maintain and follow SOPs, test methods, analytical procedures, and internal QC verification.
• Analyze and interpret test data; prepare test reports, Certificates of Analysis (CoA), and ensure accuracy & completeness of records.
• Identify, document and report Out-Of-Specification (OOS), Out-Of-Trend (OOT) results; assist in investigations, root-cause analysis, and corrective/preventive actions (CAPA).
• Participate in raw-material sampling, environmental monitoring, stability testing, and release testing as required.
Required Qualifications & Experience
• B.Sc. / B.Pharm / B.Tech (Biotechnology / Chemistry / Life Sciences) or equivalent. M.Sc. / M.Pharm / relevant post-graduate qualification is a plus.
• Minimum 3 years’ experience in QC in pharmaceutical / nutraceutical / life-sciences manufacturing environment. Experience in soft-gel manufacturing facility is preferable.
• Sound knowledge of analytical techniques (HPLC/UPLC, UV-Vis, IR, wet chemistry titrations, dissolution, pH, microbial testing if applicable).
• Understanding of cGMP, documentation practices, good laboratory practices (GLP), stability protocols, sampling procedures.
• Experience in performing OOS/OOT investigations and CAPA documentation.
Interview Process
walk – in – interview
