Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.
Post : Senior Executive / Manager 2 - Analytical Development
Job Description
1. To work as per cGMP and ensure its compliance.
2. Analytical method validation raw data & report review for different techniques like (LC-MS/GC-MS/ICP -MS/ICP OES-MS) for all regulated markets, Characterization & GMP Batch analysis.
3. To ensure that analytical work is carried out in the department in accordance with cGLP compliance/Ensure the training and QMS activities.
4. Desire knowledge of characterisation techniques such as LCMS /GCMS /ICPMS/ICP OES
5. Responsible for drafting of QMS and timely closure of QMS activity related to method validation /Batch analysis in GMP area / Any OOC during execution of calibration and CSV related activity.
6. To verify regular back up & archival activity for instrument related to Characterization.
7. Regulatory guideline knowledge for US & other advanced markets will be desired.
Additional Information
Experience : 6-12 years
Qualification : MSc / MPharm
Location : Tandalja Baroda
Industry Type : Pharma/ Healthcare/ Clinical research
Business Unit : Analytical Development
Job Grade : G11B/G11A
End Date : 30th January 2026
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