Sun Pharma is the fourth largest generic pharmaceutical company in the world. It' is also India's largest and most valuable pharmaceutical enterprise by size and market capitalization. The company provides high-quality medicines trusted by customers and patients in over 150 countries and has multiple manufacturing facilities and R & D centres. Our leadership is approachable, recognizes people's passion for growth, gives them a voice and empowers them to make a positive change.
Sun Pharma Hiring
MS&T - Injectable
Job Location : Halol
Qualification : M.Pharm
Experience : 2-10 years
Brief Job Description : 1) Responsible for executing technology transfer activities for injectable dosage forms, including planning and performing Scale-up, Exhibit and Process Validation batches with optimal utilization of manpower, materials, and equipment. 2) Provide technical support for troubleshooting during batch execution, conduct data comparison, and perform root cause investigations for deviations and process issues at Sun Pharma or CMOs. 3) Ensure compliance with cGMP and regulatory requirements while preparing and reviewing all related documentation, and coordinate effectively with cross-functional teams to achieve seamless technology transfer and validation outcomes.
MES Engineer
Job Location : Halol
Qualification : M.Pharm
Experience : 8-11 years
Brief Job Description :
1) Responsible for configuring, maintaining, and providing application support for PAS|X MES, including designing and developing Master Batch Records (MBRs) tailored to site-specific manufacturing requirements. Ensure seamless integration of PAS|X with ERP, SCADA, and PLC systems for efficient data flow
2) Guarantee compliance with GMP, GxP, and Computer System Validation (CSV) standards, and prepare and execute validation protocols using tools like KNEAT or equivalent.
3) Collaborate with cross-functional teams to deliver robust, validated MES solutions that enhance operational efficiency and regulatory compliance
Regulatory Affairs (US group)
Job Location : Vadodara
Qualification : M.Pharm
Experience : 8-14 years
Brief Job Description :
1) Develop and implement regulatory strategies for product development, submissions, and commercialization in compliance with FDA, EU, and Health Canada regulations.
2) Prepare, review, and submit regulatory dossiers (ANDA, NDA, ANDS, DCP) to secure approvals in the US, Canada, and Europe. .
3) Oversee post-approval activities including renewals, variations, and supplements for oral and non-oral products.
4) Serve as primary liaison with regulatory agencies, managing communications, briefing documents, meetings, and responses during reviews and inspections
5) Lead a team of 2–3 members, ensuring efficient performance in CMC and labeling activities; monitor submissions, query responses, and post-approval tasks.
Email your resume at : Rosemary.varghese@sunpharma.com
Last Date : 25th December 2025
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