Job Description:
Ind-Swift Laboratories Ltd. is looking for dynamic and experienced professionals to join our
Quality Control department. The ideal candidate will be responsible for ensuring the quality and compliance of
Raw Materials, Packaging Materials, Finished Goods, and Stability Samples in accordance with regulatory guidelines and company SOPs.
APPLY BEFORE: 13 July 2025
Responsibilities:
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Conduct routine analysis of Raw Materials, Packaging Materials, Finished Goods, and Stability Samples as per approved specifications and SOPs.
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Perform sampling, testing, and documentation in compliance with cGMP and regulatory standards.
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Maintain proper documentation of test results, calibration records, and instrument logs.
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Operate and maintain analytical instruments like HPLC, GC, UV-Vis, etc.
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Support investigations related to OOS, deviations, and lab incidents.
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Ensure timely completion of testing to support production and dispatch schedules.
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Collaborate with cross-functional teams to address quality-related concerns.
Preferred Qualifications:
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Educational Background: B.Sc / B.Pharma / M.Pharma / M.Sc (Chemistry)
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Experience: 2–7 years in a pharmaceutical quality control environment
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Strong understanding of cGMP, GLP, and international regulatory standards (e.g., USFDA, WHO-GMP).
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Practical knowledge of testing and documentation for raw materials, packaging, finished goods, and stability samples.
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Proficiency in operating analytical instruments such as HPLC, GC, and UV spectrophotometer.
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Good analytical skills, attention to detail, and ability to troubleshoot lab issues.
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Effective communication and coordination skills.