Executive – Analytical Development at Sun Pharmaceutical Industries Ltd, Vadodara
Sun Pharmaceutical Industries Ltd is hiring an Executive for Analytical Development in the R&D1 Regulatory Affairs business unit at Tandalja, Vadodara. This Sun Pharma hiring opening for an analytical development role requires an M.Pharm and 1 to 5 years of experience.
About the Company
Sun Pharmaceutical Industries Limited (Sun Pharma) is one of India’s largest pharmaceutical companies and a leading global speciality generics company. Founded in 1983 by Dilip Shanghvi, the company is headquartered in Mumbai, Maharashtra, and operates across more than 100 countries. Sun Pharma develops, manufactures, and markets a wide range of pharmaceutical formulations, including generic medicines, branded generics, speciality medicines, and active pharmaceutical ingredients (APIs). Its key therapeutic areas include dermatology, cardiology, psychiatry, neurology, gastroenterology, and oncology. With a strong focus on research and development, quality manufacturing, and innovation, Sun Pharma is committed to providing affordable, high-quality medicines to patients worldwide.
Job Details
- Title: Executive – ADD
- Job Title: Executive-Analytical Development
- Company: Sun Pharmaceutical Industries Ltd
- Business Unit: R&D1 Regulatory Affairs
- Job Grade: G12A
- Location: Tandalja – R&D, Vadodara
- Date: 21 October 2026
Key Responsibilities
- Strong analytical skills with a thorough understanding of performing analytical API activities in cGMP as well as Development Laboratory environments.
- Ability to work in compliance with cGMP requirements, ensuring adherence to current regulatory guidelines and established SOPs.
- Responsible for performing Method Development, Validation and Plant troubleshooting analytical activities by using HPLC, GC & Ion Chromatography techniques
- Responsible for performing the Calibration of Lab instruments like Balance, pH meter, KF Titrator, HPLC, GC and Ion Chromatography.
- To work as per cGMP and ensure its compliance as per current guidelines and SOPs
- Accountable for preparation of Validation Study Protocols and Reports, Calibration reports, Documentation as per ALCOA++, SOPs, Trainings etc.
- Systematic familiarity with digital Training and QMS tools like LMS, EDMS, LIMS & Track wise.
- Sound Knowledge about QMS activities like incidents and deviations, etc.
- Responsible for taking training before execution of allotted work.
- Responsible for understanding any non-compliance/event that occurs during execution of GMP activities
- Responsible for following safety precautions as per laboratory procedure.
- Responsible for timely archival of documents as per SOP.
- Responsible for ensuring proper handling and disposal of waste.
- Responsible for following safety precautions as per laboratory procedure
Eligibility Criteria
- Educational Qualification: M. Pharm
- Experience: Tenure 1- 5 years of experience. Sun Pharma hiring analytical development candidates should also check the full eligibility list below.
Required Skills
- Technical Competencies
- M.Sc. in Analytical Chemistry / M. Pharm in Analytical or Pharmaceutical chemistry/science
- Instrumentation knowledge of Balance, KF, GC, HPLC, IC, pH meter, UV, etc.
- Good analytical and documentation skills.
- Knowledge of MS Office (Word, Excel and PowerPoint)