Teva Pharmaceuticals, a global leader in generic and biopharmaceutical medicines, is currently conducting walk-in interviews for multiple Supervisor positions within our Production Department across India. We’re seeking highly motivated and experienced professionals to join our dynamic and inclusive team. If you’re passionate about production excellence and possess the necessary qualifications, we encourage you to attend our upcoming interview event.
Why Choose Teva Pharmaceuticals?
For over 120 years, Teva has been a pioneer in the pharmaceutical industry, consistently striving to improve global health through innovative and accessible medicines. As a global leader with a presence in 58 markets and approximately 37,000 employees worldwide, we offer a unique opportunity to contribute to a significant and impactful organization. At Teva, we foster a collaborative and inclusive work environment where every voice is heard and valued. We are committed to providing our employees with opportunities for growth and development, within a stimulating and rewarding career path.
Supervisor Production Opportunities at Teva: A Detailed Look
We are currently seeking Supervisors for several key areas within our Production Department. These roles offer the chance to lead and mentor teams while contributing to the manufacturing of high-quality medications.
Key Responsibilities:
The specific responsibilities will vary slightly depending on the assigned area (Encapsulation & Coating, Compression & Coating, or Granulation/Blending), but all positions will encompass the following core duties:
- Team Supervision and Leadership: Overseeing and managing a team of production associates, providing guidance, training, and support to ensure efficient and safe operations. This includes performance management, addressing employee concerns, and fostering a positive team dynamic.
- Production Optimization: Implementing strategies to optimize production processes, improve efficiency, and reduce waste. This may involve analyzing production data, identifying bottlenecks, and implementing solutions to maximize output while maintaining the highest quality standards.
- Quality Control and Assurance: Ensuring adherence to strict quality control standards throughout the production process. This includes reviewing and updating Standard Operating Procedures (SOPs), conducting regular quality checks, and identifying and resolving any quality-related issues.
- Documentation and Record Keeping: Maintaining accurate and up-to-date production records, including batch records, quality control reports, and other relevant documentation. This is crucial for regulatory compliance and traceability.
- Equipment Maintenance and Upkeep: Collaborating with maintenance teams to ensure that production equipment is functioning properly and is maintained according to established protocols. This helps prevent equipment downtime and ensures continuous production.
- Regulatory Compliance: Maintaining strict adherence to all relevant Good Manufacturing Practices (GMP) regulations and company policies.
Specific Area Responsibilities:
- Supervisor Production – Encapsulation & Coating: Specific expertise and experience in encapsulation and coating processes are required. You will have responsibility for the upkeep and supervision of the encapsulation and coating areas.
- Supervisor Production – Compression & Coating: Specific expertise and experience in tablet compression and coating processes are required. You will be responsible for the upkeep and supervision of the compression and coating areas.
- Supervisor Production – Granulation/Blending: Specific expertise and experience in granulation and blending processes are required. You will have responsibility for the upkeep and supervision of the granulation and blending areas.
Job Requirements
- Education: Diploma in Engineering, D.Pharm, B.Pharm, M.Pharm, B.Sc., or M.Sc.
- Experience: 4-7 years of experience in a pharmaceutical production environment, ideally in a supervisory role.
- Skills: Strong leadership, communication, and problem-solving skills. Experience in GMP and regulatory compliance is essential. Proficiency in relevant production equipment and processes is required. Experience with SOP documentation and review is also essential.
Walk-in Interview Details:
- Date: Sunday, May 4, 2025
- Time: 9:00 AM – 4:00 PM
- Venue: Teva Pharmaceuticals office
- C/O Watson Pharma Pvt Ltd, Plot A3-A6, Phase I-A, Verna Industrial Estate, Verna, Salcete, Goa, Goa- 403722.
Bring your resume and be prepared for an on-the-spot interview. We look forward to meeting you!
