Address
Form of workWho are we?
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Job Description
This position requires knowledge, experience and skills to manage quality control analytical operations with respect to biological product development, focusing on routine GMP testing, method qualification/verification/validation/transfer, and any corresponding lab investigations associated with these activities. Primary activities center on raw materials testing, product in-process testing and oversight of contract lab testing, as appropriate. The incumbent may also participate in/oversee activities related to biological product release and stability testing, reference standard establishment and management, product specification generation and maintenance and support of regulatory filing authorship/review. Assessing, improving and maintaining local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, etc.) are integral responsibilities of this position. The position will supervise resources and assets that could include a small team and multiple simultaneous development projects. The position requires demonstrated application of standard principles, theories and techniques to solve specific problems in a productive manner and the ability to manage multiple projects. Developing staff, creating opportunities for technical and personal development of the team and supporting the growth of the next generation of Teva leaders are also essential aspects of this position.
Qualifications
Required: Minimum of BS Degree in Analytical Chemistry or Biochemistry
Required: Minimum of 7 years experience in Analytical Chemistry within the Pharmaceutical industry
Required: Minimum of 3 years managerial or supervisory experience directly managing, evaluating and coaching direct reports
Preferred: MS or PhD in Analytical Chemistry or Biochemistry
Preferred: 12 years or more experience in Analytical Chemistry within the pharmaceutical industry with deep technical experience in one or more areas of biologics drug development
Function
Research & Development
Sub Function
Drug Development and Preclinical Studies
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva's Equal Employment Opportunity Commitment
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.
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Job Description
This position requires knowledge, experience and skills to manage quality control analytical operations with respect to biological product development, focusing on routine GMP testing, method qualification/verification/validation/transfer, and any corresponding lab investigations associated with these activities. Primary activities center on raw materials testing, product in-process testing and oversight of contract lab testing, as appropriate. The incumbent may also participate in/oversee activities related to biological product release and stability testing, reference standard establishment and management, product specification generation and maintenance and support of regulatory filing authorship/review. Assessing, improving and maintaining local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, etc.) are integral responsibilities of this position. The position will supervise resources and assets that could include a small team and multiple simultaneous development projects. The position requires demonstrated application of standard principles, theories and techniques to solve specific problems in a productive manner and the ability to manage multiple projects. Developing staff, creating opportunities for technical and personal development of the team and supporting the growth of the next generation of Teva leaders are also essential aspects of this position.
- Oversee QC laboratory operations:
- Support and manage release of raw materials and in process testing of biologic products and provide review and approval of documentation.
- Support and manage release of and stability testing associated with biologic products and provide review and approval of the corresponding documentation, as needed.
Qualifications
Required: Minimum of BS Degree in Analytical Chemistry or Biochemistry
Required: Minimum of 7 years experience in Analytical Chemistry within the Pharmaceutical industry
Required: Minimum of 3 years managerial or supervisory experience directly managing, evaluating and coaching direct reports
Preferred: MS or PhD in Analytical Chemistry or Biochemistry
Preferred: 12 years or more experience in Analytical Chemistry within the pharmaceutical industry with deep technical experience in one or more areas of biologics drug development
Function
Research & Development
Sub Function
Drug Development and Preclinical Studies
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva's Equal Employment Opportunity Commitment
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.
