Quality Analyst Role at Teva Pharmaceuticals USA
Looking for a rewarding quality analyst job in the life sciences field? Teva Pharmaceuticals is hiring a Quality Analyst II for the manufacturing floor in West Chester, Pennsylvania. Join a global leader in generic medicines and play a crucial role in ensuring quality, compliance, and excellence in biologics manufacturing. This is your chance to grow your career in Teva Pharmaceuticals careers.
Job Details:
- Job Title: Quality Analyst II – Quality on the Manufacturing Floor
- Location: West Chester, Pennsylvania, United States, 19380
- Company: Teva Pharmaceuticals
- Job Id: 65480
- Experience Required: Minimum 2 years in cGMP documentation and biologics/large molecule products
- Work Environment: Manufacturing floor, supporting cell bank, bulk drug substance, and drug product production
- Tools Used: Veeva, SAP, TevaDoc, LIMS, TevaLMS, Microsoft Word, Excel
5. About Teva Pharmaceuticals:
Teva Pharmaceuticals is a global leader in generic medicines and biologics, committed to making health more affordable and accessible. Operating in nearly 60 countries, Teva’s medicines are taken by over 200 million people worldwide daily. Joining Teva means contributing to a mission that directly improves global health and impacts millions of lives. Learn more in the official website of teva pharmaceuticals careers. Explore more offers similar to quality analyst job in the USA.
Educational Requirements:
- BS/BA (or higher) in a relevant life science discipline
- Preferred: Experience in biologics, large molecule products, or biopharmaceutical manufacturing
Key Responsibilities for Quality Analyst Role:
- Perform QA on the manufacturing floor for cell bank, bulk drug substance, and drug product production
- Ensure manufacturing activities follow and are documented using cGMP standards
- Support product and equipment changeovers with QA oversight
- Review and approve executed batch records and deviations/CAPAs
- Approve controlled documents, SOPs, Work Instructions, and Forms
- Support site compliance with Teva policies, regulatory requirements, and GMP guidelines
- Use Veeva, SAP, TevaDoc, LIMS, and TevaLMS to execute GMP QA activities
Skills Required for Quality Analyst Role:
- Knowledge of GMP regulations and quality compliance (cGMP, ICH, FDA, EMA, MHRA, USP/EP)
- Excellent oral and written communication skills
- Detail-oriented and highly organized
- Team player, able to collaborate across QA and Manufacturing personnel
- Proficiency in Microsoft Word and Excel
Benefits of the Quality Analyst Role:
- Comprehensive health insurance (Medical, Dental, Vision, Prescription)
- Retirement savings: 401(k) with employer match up to 6% + 3.75% Defined Contribution
- Paid Time Off: vacation, sick/safe time, caretaker time, holidays
- Life and Disability Protection: Company-paid coverage
- Additional benefits: Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Paid Parental Leave, Virtual Physical Therapy, and more
- Total compensation may include restricted stock units and discretionary awards
