Research Associate Position at Cadila Pharmaceuticals | MSc Graduates Apply Online
Looking to build a rewarding career in pharmaceutical research? Cadila Pharmaceuticals is hiring an Associate Researcher – Analytical Development Laboratory (ADL) in Dholka, Gujarat. This full-time role offers an exciting opportunity to work on analytical method development, validation, and regulatory compliance for Active Pharmaceutical Ingredients (APIs).
- Job Title: Research Associate – Analytical Development Laboratory (ADL)
- Location: Dholka, Ahmedabad, Gujarat
About The Company
Cadila Pharmaceuticals Ltd. is one of India’s largest privately held pharmaceutical companies, headquartered in Ahmedabad, Gujarat. Established in 1951, the company is known for its strong focus on research, development, and manufacturing of affordable and high-quality medicines across a wide range of therapeutic areas including cardiovascular, oncology, anti-infectives, gastroenterology, and respiratory care. With a presence in over 100 countries, Cadila operates state-of-the-art manufacturing facilities and robust R&D centers that adhere to global regulatory standards. The company is committed to innovation, accessibility, and improving healthcare outcomes worldwide through sustainable and patient-centric solutions.
Position Summary:
Cadila Pharmaceuticals is seeking a highly skilled and detail-oriented Research Associate – ADL to join its API R&D team. The candidate will handle development, validation, and transfer of analytical methods for Active Pharmaceutical Ingredients (APIs). This role ensures product quality, supports process development, and facilitates regulatory compliance across the API lifecycle.
Key Responsibilities:
- Develop and validate analytical methods for raw materials, intermediates, and APIs using HPLC, GC, UV, IR, KF, and titration.
- Support API process development by analyzing in-process samples, final products, and impurities.
- Characterize degradation products and impurities using LC-MS, GC-MS, NMR (if available).
- Perform routine and non-routine analysis to support R&D, stability studies, and method transfer activities.
- Conduct analytical method transfers to QC and manufacturing sites.
- Prepare and review analytical documentation, including method validation protocols, reports, SOPs, and COAs.
- Ensure compliance with GLP, cGMP, and data integrity standards.
- Maintain laboratory instruments and troubleshoot minor issues.
- Participate in OOS investigations, deviations, and CAPA implementations.
- Collaborate with process chemistry, regulatory affairs, and quality assurance teams.
Qualifications:
- M.Sc. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Chemistry, or related discipline.
- 2–5 years of experience in ADL for API R&D.
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