tyle="text-align: center;" data-start="254" data-end="737">MSc Analytical Chemistry Jobs at SunPharma | Apply Now for the Executive Role
Sun Pharmaceutical Industries Ltd., India’s leading pharmaceutical company, is hiring a Senior Executive/Executive – Analytical Development for its R&D unit in Baroda. This role is ideal for candidates with an M.Sc. or M.Pharm and 2–8 years of experience in analytical method validation, characterization, and compliance. At Sun Pharma, employees thrive in a culture that values growth, collaboration, and innovation while adhering to global quality and regulatory standards.
- Job Title: Senior Executive / Executive – Analytical Development
- Location: Baroda (Tandalja – R&D), India
- Company: Sun Pharmaceutical Industries Ltd.
- Business Unit: R&D1 Regulatory Affairs
- Date Posted: 04 September 2025
About Sun Pharma
At Sun Pharma, we empower individuals to “Create your own sunshine” by providing opportunities for continuous learning, professional growth, and collaboration. Our culture is built on the values of self-drive, teamwork, and innovation, where every employee is encouraged to thrive and make a meaningful impact.
Job Description
The Executive – Analytical Development will work under cGMP and cGLP compliance to support analytical method validation, characterization, and regulatory submissions for global markets.
Key Responsibilities
- Conduct analytical method validation, raw data, and report review for techniques including LC-MS, GC-MS, ICP-MS, and ICP-OES.
- Perform characterization and GMP batch analysis as per global regulatory standards.
- Ensure compliance with cGLP guidelines, QMS activities, and mandatory training requirements.
- Draft QMS documents and ensure timely closure of activities related to method validation, batch analysis, OOC handling, calibration, and CSV-related tasks.
- Monitor regular backup and archival activities for instrument characterization data.
- Apply knowledge of regulatory guidelines for the US and other advanced markets.
Job Requirements
- Education: M.Sc. (Chemistry/Analytical Chemistry) or M.Pharm
- Experience: 2–8 years in analytical development or related functions
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Desired Skills:
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Strong knowledge of LC-MS, GC-MS, ICP-MS, and ICP-OES techniques
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Familiarity with QMS, cGMP, cGLP, and global regulatory compliance
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Experience in handling method validation and GMP batch analysis
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Disclaimer: This job description outlines the general nature and responsibilities of the role. It may be updated periodically to align with business needs and the incumbent’s experience.
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