We’re Hiring! Join Our QA – Validation & Qualification Team 🔬
📍 Location: Bavla, Ahmedabad
🔍 Industry: Pharmaceutical Manufacturing (Must have Parenteral background)
At Swiss Parenteral, we are committed to maintaining the highest quality standards across our WHO-GMP, ISO 9001:2008 certified manufacturing units. With facilities aligned to EU, USFDA, TGA, and MCC requirements, we take pride in our robust quality systems and regulatory compliance.
We’re looking for QA professionals who are passionate about validation, documentation, and continuous improvement.
🔧 Key Responsibilities:
✅ Equipment qualification – HVAC, Autoclave, Vial Washing, Tunnel, etc. (IQ/OQ/PQ)
✅ Process validation, cleaning validation & media fill execution
✅ Temperature mapping & calibration monitoring
✅ SOPs – preparation, review, training & implementation
✅ Review of BMRs, protocols, master documents
✅ Participation in internal audits & vendor audits
✅ Ensuring compliance with cGMP and plant hygiene standards
🎯 What We’re Looking For:
✔️ 2–5 years of relevant experience in a regulated pharmaceutical environment
✔️ Must have experience in Parenteral Manufacturing
✔️ Strong understanding of GMP, validation, and documentation practices
✔️ Good communication and cross-functional coordination skills
📩 Apply Now!
If you’re ready to grow your career with a globally recognized pharmaceutical company, we’d love to hear from you.
📧 Email: hr1@swiss.in
📞 Contact: +91 6352978952
🌐 Website: www.swiss.in
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