Pharmaceutical Documentation Associate

9 hours ago

Ahmedabad, Gujarat, India Swiftmed International Private Limited Full time ₹ 9,00,000 - ₹ 12,00,000 per year

As a Pharmaceutical Documents Associate at our company, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your responsibilities will include: - Having experience or sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards, Quality Management, and Quality Control. - Demonstrating knowledge or experience in Quality control tests for various formulations and APIs such as Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc using methods like HPLC, GC, TLC, IR/UV, Disso, etc. - Understanding pharmacopoeia applications and all documentation relevant to QA/QC. - Preparing documents like BMR, SPEC, STP, AMV/PDR Protocol, Report, and other necessary documents. Your duties will involve: - Preparing documents related to QA/QC and regulatory requirements. - Collaborating with regulatory, production, and quality teams to enhance process efficiencies and compliance. - Maintaining accurate and up-to-date documentation following Good Documentation Practices (GDP). The ideal candidate for this role should have: - Diploma in a related field. - At least 1 year of experience in the pharmaceutical industry. Benefits of joining our team include: - Flexible schedule. - Paid sick time. If you meet the above criteria and are located in or willing to relocate to Ahmedabad, Gujarat, we encourage you to apply for this full-time position. Day shift and night shift availability are preferred for this role. Only candidates meeting the specified criteria will be considered for an interview.,

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