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Senior Manager R&D Team Leader

Company: Teva Pharmaceutical Industries
Location: West Chester
Posted on: June 12, 2021

Job Description:

Company Info

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!

R&D:

Teva's Global Research & Development (R&D) organization is devoted to the development of new medicines, devices and combination products that provide meaningful therapeutic benefit to patients worldwide. Combining creativity, scientific rigor and our extensive knowledge on a broad range of technologies, our scientists, engineers, medical doctors and project leaders across the globe use their expertise to innovate novel biologics, biosimilars, small molecule specialty medicines, generics and over-the-counter therapies

Job Description

This position requires knowledge, experience and skills to manage an analytical group for a quality control operation in a biologics pharmaceutical team, focusing on release testing, raw materials testing, in process testing for biological products and the corresponding lab investigations. Assessing, improving and maintaining local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, etc) are integral responsibilities of this position. The incumbent 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.

Essential Duties & Responsibilities:

  • Oversee QC laboratory operations, support and manage release, raw materials and in process testing of biologic products and provide review and approval of documentation.
  • May manage method transfer and validation activities.
  • Initiate, prepare, evaluate and recommend actions regarding proposals for improved analytical methods.
  • Maintain compliance with applicable ICH, GxP and safety regulations.
  • Identify, write, revise, manage and implement standard operating procedures, work instructions, standard practices, protocols and reports.
  • Support QC lab investigations, compliance and audits.
  • Develop staff to ensure their skill match roles, improving productivity and efficiency of the department operation.
  • Participate in budget planning including capital equipment budgets. Propose capital purchases and execute purchases.
  • Actively contribute to the maintenance of a clean, safe working environment in the laboratories.

Qualifications

Education:

  • Minimum BS in Analytical Chemistry, Biochemistry or Biology
  • Preferred MS in Analytical Chemistry, Biochemistry or Biology

Experience:

  • Required PhD with 0 years or BS/MS with 10 years experience in Analytical Chemistry within the pharmaceutical industry and a minimum 3 years of supervisory or management experience.
  • Preferred PhD with 2 years experience in Analytical Chemistry within the pharmaceutical industry and minimum 3 years of supervisory or management experience.

Function

Research & Development

Sub Function

Drug Development and Preclinical Studies

Reports To

Dir US Quality Control & Analytical Operations R&D

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.

Nearest Major Market: Philadelphia

Keywords: Teva Pharmaceutical Industries, Wilmington , Senior Manager R&D Team Leader, Other , West Chester, Delaware

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