Job Opportunity: Research Associate / Senior Research Associate – ARL (Documentation)
📍 Location: Dholka Plant
🏢 Department: ARL – Documentation
💼 Designation: Research Associate / Senior Research Associate
🕛 Experience Required: 1-5 Years
About Cadila Pharmaceuticals
Cadila Pharmaceuticals is a globally recognized leader in innovative and affordable healthcare solutions. With a strong commitment to R&D, compliance, and quality, we deliver life-changing medicines worldwide. Join our dynamic team and contribute to scientific excellence in the pharmaceutical industry!
Key Responsibilities
✔ Ensure GLP compliance as per regulatory standards.
✔ Maintain records of reference standards, working standards, and impurity standards.
✔ Manage HPLC column records and instrument calibration (HPLC, UV, GC, LC-MS/MS, etc.).
✔ Perform daily calibration of lab equipment (pH meters, refrigerators, thermometers).
✔ Prepare and revise SOPs for the Analytical Laboratory.
✔ Maintain LNB and MRS records for validation & development.
✔ Generate indents for lab supplies (chemicals, solvents, columns, etc.).
Key Requirements
✔ 1-5 years of experience in pharma documentation & compliance.
✔ Strong knowledge of GLP, analytical instruments, and calibration processes.
✔ Experience in SOP drafting & lab record maintenance.
✔ Detail-oriented with excellent organizational skills.
✔ Educational Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm (Relevant Discipline).
Why Join Cadila Pharmaceuticals?
✅ Industry Leader – Work with a globally trusted pharma brand.
🔬 Innovation-Driven – Be part of cutting-edge pharmaceutical research.
📈 Career Growth – Competitive salary & advancement opportunities.
👥 Collaborative Culture – Join a team passionate about scientific excellence.
How to Apply
📩 Send Your Resume To: [drashti.chaudhari@cadilapharma.com]
Important Note
Cadila Pharmaceuticals is an equal-opportunity employer. Hiring is based on merit and qualifications – no recruitment fees are involved. Beware of fraudulent job offers.
