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Chemical Process Engineer III

Date: Jan 12, 2021

Location: Cincinnati, Ohio, US, 45213

Company: Teva Pharmaceuticals

Company Info

Teva is searching for a Chemical Process Engineer III 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.

Job Description

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


  • Bachelor’s Degree in Science related - required. Engineering strongly preferred.
  • 10+ years Pharmaceutical validation (Process validation) required
  • 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 and FDA guidelines required.
  • Apply working knowledge of regulatory requirements and other related disciplines.
  • Understanding of departmental working relationships



Sub Function

Technical Transfer

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.

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: Cincinnati