1+ months

Sr. Manager Manufacturing Science & Technology

Salt Lake City, UT 84111

Company Info

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve 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 our facility in the International Center, near the Salt Lake City International Airport (4745 Wiley Post Way, 84116).

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

Job Description

 

POSITION SUMMARY

This position is responsible for leading and managing the site MS&T team including the initiation, execution and management of departmental projects (including R&D support, scale up and validation) to support a consistent supply of quality drug product to the market. This position will manage cleaning and process validation activities, technology transfer and provide formulation and process related technical support to groups such as Production, QA, QC and third party personnel for the companys solid dosage commercial products. This position is responsible for ensuring that activities meet critical project deadlines and product launch dates.

 

ESSENTIAL AREAS OF RESPONSIBILITY

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary.  Any non-essential functions are assumed to be included in other related duties or assignments.

 

  • Responsible for the daily management and development of direct and indirect reports.
  • Responsible for providing direction, coordinating project tasks, team responsibilities and timelines and assure results are produced.
  • Responsible for assisting with departmental goal establishment and monitor to effectively accomplish specific team objectives.
  • Responsible for the design and execution of experiments to optimize and scale-up drug process operations such as blending, compression, granulation and coating of solid dose formulations.
  • Responsible for preparing and/or reviewing documents to support projects such as change controls, protocols, master batch records, investigation reports, SOPs, etc.

Qualifications

 

POSITION REQUIREMENTS

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

 

Education/Certification/Experience:

  • Requires BS, MS or PhD degree or equivalent in a scientific or related discipline.
  • Requires a minimum of 10 years relevant progressive pharmaceutical experience in process and cleaning validation/technical services or related experience.
  • Requires a minimum of 3 years managerial experience of a technical group.
  • Requires experience with solid dosage manufacturing with an in-depth understanding of process validation, Quality by Design, quality assurance, quality system and regulatory requirements for global markets.
  • Requires working knowledge of raw material physical properties and relevance to solid dosage forms, equipment and unit operations associated with blending, milling, granulation, drying, compression and coating.

Function

Manufacturing

Sub Function

Technical Transfer

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: 2019-10-04 Expires: 2019-11-24

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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Sr. Manager Manufacturing Science & Technology

Teva Pharmaceuticals
Salt Lake City, UT 84111

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