Quality Sr Specialist Job at Teva Pharmaceuticals – Apply Now!
Are you passionate about ensuring the highest standards of quality in the pharmaceutical industry? Teva Pharmaceuticals is looking for a dedicated Quality Sr Specialist to join our team in Bangalore, India. If you have a background in QA/QC and a keen eye for compliance, this could be the perfect opportunity for you!
About Teva Pharmaceuticals
At Teva Pharmaceuticals, we are committed to making affordable and high-quality healthcare accessible to millions worldwide. As a global leader in generic medicines and an industry pioneer, our products touch the lives of over 200 million people daily. With a presence in nearly 60 countries, we manufacture a wide range of medicines, including those on the World Health Organization’s Essential Medicines List. Innovation, excellence, and patient-centric solutions drive our mission as we continue shaping the future of healthcare.
Job Description of Quality Sr Specialist Job:
Job Title: Quality Sr Specialist
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job Id: 61074
The Opportunity of Quality Sr Specialist Job
This incumbent ensures that the review of CMC documentation is completed in a timely and compliant manner as per Teva CORP standards and related guidance. The responsibilities include
reviewing Method Development/Validation Protocols & Reports, Stability Protocols & Reports, Instrument/Equipment Qualification records, and more.How You’ll Spend Your Day
Review of CMC Documentation:
- Review of Method Development/Validation protocols & reports
- Review of Stability Study protocol, reports & grids
- Review of Instrument/Equipment Qualification records
- Review of Batch Manufacturing Records
Quality Management Systems
The owner of the function initiates the process of change controls and deviations, prepares local SOPs and related documents, participates in the self-inspection process, and more.
Your Experience and Qualifications for the Quality Sr Specialist Job
- Master’s or Bachelor’s Degree in Pharmacy or Natural Sciences
- Experience: 2-8 years in QA/QC function within the pharmaceutical industry
Skills Required:
- Strong knowledge of cGxP regulations
- Experience in CMC documentation review & compliance
- Excellent communication and documentation skills
Keywords: Teva Pharmaceuticals, Quality Sr Specialist, Pharmacy, QA/QC, Pharmaceutical Industry, cGxP Regulations, SOPs, Quality Management.
