5 days old

Manager Q.C. Raw Materials

West Chester, PA 19380
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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!
Job Description

This Manager Q.C. Raw Materials position requires knowledge, experience and skills to manage an analytical group for a quality control operation, focusing on release and raw materials testing and 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, manage release and raw materials testing 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:

BS in Chemistry or related sciences required, MS a plus

 

Experience:

Required: At least 5+ years of GMP QC Lab experience,

1 + year experience as a Lead or Manager desired in Analytical Chemistry within the pharmaceutical industry.

Experience with Raw Materials required.  Strong leadership and collaboration skills required. 

Function
Research & Development
Sub Function
Pharma R&D Project/Program Management
Reports To
In process of validation
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.

Posted: 2020-02-15 Expires: 2020-03-16

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Manager Q.C. Raw Materials

Teva Pharmaceuticals
West Chester, PA 19380

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