Research Job at Teva Pharmaceuticals | Apply Now For The Analytical Researcher Role
Teva Pharmaceuticals is hiring an Analytical Researcher I in Goa, India. This is a great opportunity for experienced professionals in analytical chemistry and quality control to work with one of the world’s leading pharmaceutical companies. If you’re passionate about laboratory excellence, regulatory compliance, and innovative research in solid oral dose formulations, this position offers a rewarding career path.
- Job Position: Analytical Researcher I
- Location: Goa, India, 403722
- Job ID: 64158
About the Company
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to making healthcare more accessible and affordable. Operating in nearly 60 countries, Teva manufactures many of the essential medicines listed by the World Health Organization. Every day, more than 200 million people rely on Teva’s medicines. The company continues to innovate and expand its impact on global health, driven by a mission to improve lives worldwide.
Job Description
As an Analytical Researcher I, you will play a crucial role in maintaining laboratory quality standards, ensuring compliance with regulatory requirements, and supporting product development through analytical excellence. This position requires hands-on experience in quality control laboratories, method validation, and regulatory submissions.
Key Responsibilities for Research Job at Teva Pharmaceuticals
- Maintain Good Laboratory Practices (GLP) and laboratory workspace.
- Conduct timely analysis and reporting of finished products and ancillary items according to production schedules.
- Maintain test procedures for raw materials and ancillary items.
- Send samples to external laboratories and conduct vendor approval sample analysis.
- Follow SOPs and instructions per GLP standards.
- Participate in method transfer and validation for new projects within committed timelines.
- Report laboratory investigations of OOS, OOT, action limits, aberrant analytical test results, chromatographic errors, and deviations.
- Maintain and manage the sample storage area.
- Participate in regulatory audit activities (e.g., USFDA, MHRA).
- Demonstrate awareness of ANDA regulatory submission processes.
- Troubleshoot issues in newly developed products.
- Ensure timely disposition of samples and calibration of laboratory instruments.
- Perform additional responsibilities as assigned by the Section Head.
Qualifications for Research Job at Teva Pharmaceuticals
- B.Sc. or M.Sc. in Chemistry.
- 3–10 years of relevant experience in a quality control laboratory.
- Exposure to regulatory audit agencies and familiarity with analytical techniques and regulatory submissions.
Benefits of Joining Teva Pharmaceuticals
- Work with a global leader in the pharmaceutical industry.
- Engage with cutting-edge research, analytical techniques, and regulatory compliance.
- Exposure to international regulatory standards and audits (USFDA, MHRA).
- Inclusive, diverse, and supportive work environment.
- Opportunities for professional growth and learning in a dynamic R&D environment.
- Contribute to medicines that impact over 200 million people globally.
