Are you a passionate chemist seeking a dynamic role in pharmaceutical quality control? Teva Pharmaceuticals, a global leader in generics and biopharmaceuticals, is hiring an Analytical Researcher I (OSD) in Goa. This is your chance to contribute to cutting-edge pharmaceutical research, ensuring high-quality oral solid dosage (OSD) products while advancing your career in a supportive, innovative environment. Join Teva and make a difference in global healthcare.
Job Responsibilities
As an Analytical Researcher I (OSD) at Teva Pharmaceuticals in Goa, you will play a critical role in ensuring product quality and compliance. Key responsibilities include:
- Ensuring adherence to Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).
- Maintaining laboratory workspaces and calibrating instruments for optimal performance.
- Conducting timely analysis and reporting of finished products, stability studies, and ancillary items.
- Updating and maintaining test procedures for raw materials and ancillary items.
- Sending samples to external laboratories and conducting vendor approval sample analysis.
- Participating in method transfers and validation activities for new pharmaceutical projects.
- Investigating Out of Specification (OOS), Out of Trend (OOT) results, action limits, and chromatographic errors.
- Maintaining an audit-ready sample storage area for regulatory inspections (e.g., USFDA, MHRA).
- Supporting ANDA regulatory submissions with a basic understanding of requirements.
- Troubleshooting issues with newly developed products and ensuring timely sample disposition.
- Taking on additional tasks as assigned by the Section Head.
Qualifications & Experience
To excel in this role, candidates must meet the following requirements:
- Education: B.Sc. or M.Sc. in Chemistry from a recognized institution.
- Experience: 3–10 years in a Quality Control Laboratory, preferably in the pharmaceutical industry.
- Strong understanding of GLP, SOPs, and regulatory compliance (USFDA, MHRA).
- Ability to troubleshoot and analyze pharmaceutical products effectively.
- Excellent organizational and communication skills.
Benefits of Working at Teva Pharmaceuticals
Joining Teva Pharmaceuticals offers a range of benefits, including:
- Competitive Salary: INR 4,00,000–8,00,000 per annum, based on experience.
- Opportunities for professional growth in a global pharmaceutical leader.
- Access to cutting-edge laboratory facilities and ongoing training.
- Supportive work environment fostering innovation and collaboration.
- Comprehensive health and wellness benefits.
How to Apply
Ready to take the next step in your pharmaceutical career? Send your updated CV to Apeksha.Shinde01@teva.co.in with the subject line “Analytical Researcher I (OSD) – Goa Application.” Ensure your CV highlights relevant experience in pharmaceutical quality control and GLP compliance. Applications are reviewed on a rolling basis, so apply by October 27, 2025, to be considered.
FAQs
Q: What is the role of an Analytical Researcher I (OSD) at Teva?
A: The role involves conducting quality control analysis for oral solid dosage products, ensuring compliance with GLP, SOPs, and regulatory standards like USFDA and MHRA.
Q: What qualifications are required for this position?
A: Candidates need a B.Sc./M.Sc. in Chemistry and 3–10 years of experience in a pharmaceutical quality control laboratory.
