Teva Career Opportunity | MS&T Specialist Role | Apply Now
Teva Pharmaceuticals is hiring for the role of MS&T Specialist I, offering a strong opportunity for pharmacy professionals to work in a high-impact manufacturing science and technology environment. This pharma job focuses on real-time process validation, product launches, and technical support for global pharmaceutical operations. It is a valuable opportunity within the growing Teva career ecosystem for candidates looking to strengthen their expertise in manufacturing, quality systems, and process development.
- Job Title: MS&T Specialist I – Manufacturing Science & Technology
- Location: Goa, India
About the Company – Teva Pharmaceuticals
Teva Pharmaceuticals is a leading global biopharmaceutical company known for its strong generics portfolio and innovation in specialty medicines. A Teva career offers exposure to global manufacturing standards, regulatory compliance, and advanced pharmaceutical technologies. This pharma job provides an opportunity to work in a high-performance environment focused on quality, safety, and continuous improvement.
Job Description
In this pharma job, the MS&T Specialist I will be responsible for supporting new product launches, process validation, troubleshooting, and product robustness programs. The role involves ensuring quality compliance, process understanding, and technical documentation support across manufacturing operations within a Teva career environment.
Key Responsibilities
- Prepare technical documentation, including batch records, protocols, and reports
- Plan and execute scale-up, transfer, and validation batches
- Support new product launches and process validation activities
- Coordinate with cross-functional manufacturing and quality teams
- Ensure GMP compliance and regulatory adherence in all operations
- Handle investigations, including deviations, CAPA, and OOS cases
- Perform root cause analysis and ensure closure of quality events
- Work with TrackWise and SAP for quality and material management
- Support regulatory submissions with technical documentation
Eligibility Criteria
- Education: B Pharm / M Pharm
- Experience: 3–4 years in MS&T or related pharmaceutical manufacturing roles
Required Skills
- Experience in new product submissions and launches
- Knowledge of material change and site transfer activities
- Strong understanding of process validation and scale-up activities
- Hands-on experience with TrackWise and SAP systems
- Knowledge of GMP and regulatory compliance requirements
- Experience in granulation, compression, encapsulation, and coating processes
- Strong documentation and technical reporting skills
- Ability to work in cross-functional manufacturing teams
- Understanding of global regulatory markets (US, EU, Canada, etc.)
This pharma job at Teva Pharmaceuticals (Teva Pharmaceuticals) offers a strong Teva career opportunity for experienced pharmacy professionals in MS&T. The role provides exposure to advanced manufacturing science, process validation, and global quality systems, making it ideal for professionals looking to grow in pharmaceutical production and technology-driven environments.
