Teva Hiring B Pharm & M Pharm Professionals | S&T Specialist Role | Apply Now
Looking for a B Pharm Job in pharmaceutical manufacturing, technology transfer, and process validation? Teva Pharmaceuticals is hiring an S&T Specialist I in Goa. This Teva Career opportunity is ideal for B Pharm and M Pharm professionals with experience in Manufacturing Science & Technology (MS&T), new product launches, process validation, and pharmaceutical operations. Candidates seeking an advanced M Pharm Job in a global pharmaceutical organization should explore this opportunity.
- Job Title: S&T Specialist
- Job Location: Goa, India
About the Company
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, combining innovative medicines with a world-class generics business. The company develops and delivers high-quality medicines across multiple therapeutic areas while serving patients worldwide. A Teva Career provides professionals with opportunities to work on innovative pharmaceutical technologies, global product launches, regulatory projects, and advanced manufacturing processes. For candidates seeking a rewarding B Pharm Job or M Pharm Job, Teva offers a collaborative environment focused on innovation, quality, and professional growth.
Job Description
The S&T Specialist I will support new product launches, process validation, technology transfer, scale-up activities, and manufacturing troubleshooting. This B Pharm Job involves the preparation of technical documentation, execution of validation batches, handling quality systems, and the support of regulatory submissions while ensuring compliance with GMP and global regulatory requirements. Through this Teva Career opportunity, professionals will gain exposure to advanced pharmaceutical manufacturing and product lifecycle management.
Key Responsibilities
- Support new product launches and site transfer activities.
- Execute scale-up, transfer, and validation batches.
- Troubleshoot manufacturing and process-related issues.
- Prepare batch records, protocols, and technical reports.
- Manage Change Controls, Deviations, CAPA, and Investigations.
- Ensure GMP and regulatory compliance.
- Coordinate with manufacturing, quality, and regulatory teams.
- Support regulatory submissions and technical documentation.
- Handle TrackWise and SAP documentation activities.
Eligibility Criteria
- Education: B. Pharm, M. Pharm
- Experience: 3–4 years of experience in MS&T or pharmaceutical manufacturing operations
- Required Skills: TrackWise, SAP, Risk Assessment, technical Documentation, Granulation, Compression, Encapsulation, Coating Operations, GMP Compliance, Regulatory Documentation, Global Market Requirements
Why Join Teva Pharmaceuticals?
- Join a globally recognized pharmaceutical company.
- Gain exposure to new product launches and technology transfer.
- Work on scale-up and process validation projects.
- Build expertise in pharmaceutical manufacturing and regulatory operations.
- Grow your career through a rewarding Teva Career pathway.
