Teva Pharmaceuticals is seeking candidates for the position of MS&T Technician II in Goa, India. The role focuses on manufacturing science and technology activities, including scale-up batches, technology transfers, new product launches, process validation, technical documentation, and shop-floor support.
Candidates with 1–5 years of experience in Manufacturing Science and Technology (MS&T) and experience in process validation, new product submissions, and launches are encouraged to review the opportunity. An M.Pharm qualification is preferred.
Job Details
| Particulars | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Job Title | MS&T Technician II |
| Job ID | 69880 |
| Location | Goa, India |
| Experience | 1–5 years in MS&T |
| Preferred Qualification | M.Pharm |
| Functional Area | Manufacturing Science & Technology (MS&T) |
Position: MS&T Technician II
The MS&T Technician II will support new product projects, process validation, scale-up activities, product launches, and market support programs. The role requires technical documentation, cross-functional coordination, quality system management, and compliance with GMP and regulatory requirements.
Roles and Responsibilities
1. Technical Documentation
- Prepare batch records, protocols, and technical reports.
- Maintain complete documentation for scale-up, technology transfer, new product launch, and validation batches.
- Provide technical documentation and responses to Regulatory Affairs for submissions and variations.
2. Scale-Up and Process Validation
- Prepare and execute scale-up batches, transfer batches, new product launches, and validation batches.
- Support process validation activities using knowledge of unit operations, analytical techniques, and statistics.
- Identify critical process parameters and material attributes that influence final product quality.
- Assess process parameters and material attributes to establish process understanding and design space.
3. New Product Projects and Market Support
- Support new product projects and process validation activities.
- Provide market support on the shop floor.
- Coordinate with cross-functional teams to support project execution.
4. Quality Systems and Investigations
- Manage change controls, deviations, investigations, CAPA, and Out-of-Specification (OOS) cases.
- Perform root cause analysis and support timely investigation closure.
- Handle quality system documentation.
5. GMP and Regulatory Compliance
- Ensure compliance with GMP guidelines, safety procedures, and regulatory requirements.
- Support Regulatory Affairs activities through technical documentation and responses.
- Use relevant systems, including TrackWise and Veeva.
Eligibility and Qualifications
Candidates should have the following qualifications and experience:
- Experience: 1–5 years in Manufacturing Science and Technology (MS&T).
- Preferred qualification: M.Pharm.
- Relevant experience: New product submissions and launches, scale-up activities, and process validation documentation and execution.
- Systems experience: TrackWise, Veeva, Glorya, and SAP.
Required Skills
- Manufacturing Science and Technology (MS&T)
- Scale-up and technology transfer batches
- New product submissions and launches
- Process validation documentation and execution
- Technical report and batch record preparation
- Critical process parameter identification
- Material attribute and process risk assessment
- Change control and deviation management
- Root cause analysis and CAPA
- Out-of-Specification (OOS) handling
- GMP and regulatory compliance
- TrackWise, Veeva, Glorya, and SAP
Benefits at Teva
Teva describes the following employee benefits and development opportunities:
- Annual leave and reward plans
- Flexible working schedules, depending on the role
- Access to tailored health support
- Community involvement opportunities
- Career development through the Twist platform, including learning programs, short-term projects, and internal growth opportunities
