MS&T Specialist

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Mainly Responsible for New product Launch projects, process validation, Troubleshooting execution of the product robustness program and Market support program on the shop floor. Risk assessment of process parameters and material attributes with combination of prior knowledge of experiments to establish a design space or other representation of process understanding. Identify the critical process parameters and input material attributes that must be controlled to achieve quality attributes of the final product.

Utilization of Knowledge of unit operations, analytical and statistics for process validation activity. Handling of investigations and quality system documents.

• Technical documentation such as batch records, protocols, and technical reports.
• Planning, preparation, and execution of scale‑up batches, transfer batches, new product launches, and validation batches with end‑to‑end documentation compliance.
• Coordination with cross‑functional teams.
• Support to the Regulatory Affairs team by providing technical documentation and responses required for regulatory submissions and variations.
• Ensuring strict compliance with GMP guidelines, safety procedures, and regulatory requirements in all operational activities.
• Hands‑on experience with Track Wise and SAP for quality events, materials, and documentation management.
• Active involvement in Change Control, Deviations, Investigations, CAPA, and Out‑of‑Specification (OOS) handling, including root cause analysis and closure.

• Experience in MS&T about 3-4 years.
• Qualification :
  
  B.Pharm/M.Pharm
• Experience in:
  • New submissions & launches
  • Material change
  • Site transfer activities
  • Scale up & process validation documentation and execution.
  • Handling of Trackwise & SAP.

• Good experience in handling Granulation, Compression, Encapsulation & Coating process and equipment.
• Knowledge on Regulatory requirements of different markets like, Europe, Canada, US and Internation markets.

At Teva India, care is at the heart of how we work. From your first day, you’ll be welcomed into a people‑first culture built on inclusion, respect, and belonging.

That support extends to you and your loved ones through benefits designed for real life. These include comprehensive medical insurance, OPD coverage, annual health checkups, term life and accident insurance, and confidential emotional wellbeing support through our Optum Employee Assistance Program. You’ll also enjoy healthy meals at work, holistic wellbeing initiatives, and volunteering programs that help you give back to the community.

Your growth matters too. You’ll have opportunities to build future‑ready skills, collaborate on projects with global teams, explore internal career opportunities, and learn through programs such as our AI‑enabled Teva Twist program, R&D Academy, continuing education, and mentorship.

Join our vibrant workplace, where we celebrate milestones, festivals, achievements, and community impact together.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all.

If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.