1+ months

Associate Director Plant/Site Quality Control

Cincinnati, OH 45202

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!

We offer a competitive benefits package including Medical, Dental, Vision and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 6% match on  the 401(k), Employee Stock Purchase Plan and Tuition Assistance.

 

This position is located at 5040 Duramed Rd, Cincinnati, OH 45213.

 

 

For more on Teva, check us out at www.tevapharm.com or www.tevausa.com.

Job Description

Position Summary:  Direct and oversee the chemical and microbiological testing and auditing of raw materials, work in progress (WIP), finished product and stability samples in the Ohio laboratory in compliance with all standard operating procedures and test methods.  Develop/optimize and validate methods and automated approaches and method transfers as required by regional QC laboratories. Liaise with R&D to coordinate testing of actives excipients and pre-commercial stability samples.

 
 

Essential Duties & Responsibilities

  • Lead the Quality Control Laboratory related activities, including commercial and development products, in order to meet site goals and objectives (quality, safety, cost, and customer service).
  • Ensure the department is supported by experienced, trained and capable management and staff to control and assure the purity, efficacy, quality and strength of product manufactured at the site. 
  • Coach, counsel and mentor staff on issues relating to job activities and career development.
  • Is accountable for the performance and results of multiple related units
  • Develops departmental plans, including business, production and/or organizational priorities
  • Lead a culture of operational excellence.  Provide recommendations for new equipment and processes that lead to an efficient and effective production environment. Continuously look for new, innovative ways to increase productivity and efficiency and decrease cost.
  • Identify new approaches, systems and/or technologies to improve quality and productivity for both the functional and business unit. 
  • Translate the site strategic plan to develop a workforce plan (capabilities, roles, headcount, culture).  Develop the laboratory management team to balance structural effectiveness with flexible capabilities.
  • Empower team to ensure ability to manage the day to day activities and problems as well as uncertainty and changing business needs. Create an environment that encourages individual contributors to raise and lead efficiency ideas.
  • Develop and implement long term goals and objectives for Quality Management to meet the demands of the business while maintaining operational quality and compliance of TUSA with applicable local policies and government regulations.

Qualifications

Education Required:

BS degree in scientific or healthcare discipline, or equivalent combination of education and experience

Education Preferred

R. Ph. or Pharm.D. MS or Ph.D. in scientific or healthcare discipline or equivalent combination of education and related experience.

Experience Required:

Minimum 8 years management level experience in pharmaceutical regulatory environment.

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

In process of validation

Tevas 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.

Categories

Posted: 2019-06-28 Expires: 2019-10-19

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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Associate Director Plant/Site Quality Control

Teva Pharmaceuticals
Cincinnati, OH 45202

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