1+ months

Sr Pharmaceutical Process Validation Engineer

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Company Info

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.

Tevas Cincinnati production site is one of our solid manufacturing and supply chain operations.

We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success. Be part of it!

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

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

Teva is searching for a Chemical Process Engineer to join our team in Cincinnati, OH!
The Chemical Process Engineer is primarily responsible for non-traditional dosage forms related to polymers. You will serve to act as the bridge between Engineering and Commercial activities, responsible for coordinating excellent processes and their successful hand-off to routine production.

In this role, you will:

  • Prepare process validation and performance qualification protocols, report and analyze data including statistics 
  • Monitor validation/re-validation, and perform qualification processes to ensure strict accordance with documentation
  • Perform routine to complex investigations
  • Assure compliance to GMP requirements for oral solid and other dosage forms including combination products
  • Perform steps to evaluate material changes and alternate materials
  • Perform hands-on process/product scale-up studies on specifically assigned products
  • Utilize knowledge in the areas of formulation development and process optimization using pharmaceutical processes such as polymer processing, terminal sterilization, wet granulation (high shear and fluid bed), pellet processes, direct compression (v-blenders and container blending systems), tablet compression, encapsulation, tablet coating, etc.
  • Contribute to process improvements
  • Resolve problems using existing solutions and new perspectives
  • Provide informal guidance to junior staff
  • Work both independently, and with more experienced mentor
  • Act as a resource for colleagues with less experience
Qualifications
  • Bachelors Degree required
  • 5+ years Pharmaceutical validation required. 10 years preferred.
  • Specialized or Technical Knowledge Licenses, Certifications needed
  • Proficient use of specified computer software
  • Ability to work under minimal supervision and ability to work collaboratively required
  • Ability to present information verbally and in writing to peers, work groups and management
  • Sound interpersonal skills
  • Working knowledge of related equipment and processes required
  • GMP including SUPAC
  • Apply working knowledge of regulatory requirements and other related disciplines.
  • Understanding of departmental working relationships
Function
Manufacturing
Sub Function
Technical Transfer
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: 2020-08-28 Expires: 2020-11-23

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 Pharmaceutical Process Validation Engineer

Teva Pharmaceuticals

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