Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

The incumbent should possess a practical understanding of bio-pharmaceutical Raw material sampling, testing and GxP requirements. This analytical laboratory position requires demonstrated application of standard principles, theories and techniques to solve specific problems in a productive manner. Assessing, improving and maintaining local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc) are integral responsibilities of this position. The position requires independence, technical expertise, ability to perform complex work as well as routine work following written procedures and ability to work on multiple projects. The position will develop, validate and perform analytical testing activities within a GxP-compliant laboratory to support pre-clinical studies, clinical development, method transfer and validation for quality control operations.

How you’ll spend your day

• Participate in method transfer and validation activities.
• Hands on experience with Change controls, Deviations and CAPA is required.
• Perform Raw material sampling, testing, record data as per GxP requirements.
• Lead and support GMP compliances and general QMS activities.
• Respond to technical questions and problems.
• May develop/perform analytical method optimization and process optimization testing.
• Maintain compliance with applicable ICH, GMP and safety regulations. Notify management of unexpected results, procedural deviations and equipment problems.
• May participate in the writing and review of standard operating procedures, work instructions, protocols and reports.
• Maintain a collaborative working relationship with external manufacturing/testing partners and other Teva departments during transfer and routine analysis.
• Actively contribute to the maintenance of a clean, safe working environment in the laboratories.
• Ensure activities are performed//completed using current Good Manufacturing Practices.
• Participate in laboratory investigations.

Your experience and qualifications

• Bachelor’s degree in scientific discipline (Chemistry, Biochemistry, Biology) + At least 5 years of experience in GMP pharmaceutical environment.

OR

• Master’s degree in scientific discipline (Chemistry, Biochemistry, Biology) + At least 2 years of experience in GMP pharmaceutical environment.

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Reports To

Senior Manager, Quality Control

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Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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