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Chemical Process Engineer I

Date: Jun 22, 2022

Location: Cincinnati, Ohio, US, 00000

Company: Teva Pharmaceuticals

Who are we?

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

Prepare process validation and performance qualification protocols, reports and analyze data.  Review work orders in data stream, review and approve equipment periodic reviews, review and approve equipment qualification protocols & reports. Monitor validation and performance qualification processes to ensure strict accordance with documentation. 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 wet granulation (high shear and fluid bed), pellet processes, direct compression (v-blenders and container blending systems), tablet compression, encapsulation, tablet coating, etc.
 

Qualifications

Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.

  • Associates Degree required
  • Bachelor’s Degree preferred
  • 1 – 3 years pharmaceutical MFG or Validation required 
  • 3 – 5 years pharmaceutical Validation preferred
  • Proficient use of specified computer software.
  • Ability to work under minimal supervision.
  • Ability to present information verbally and in writing to peers, work groups and management.
  • Apply working knowledge of equipment and processes.
  • Apply working knowledge of regulatory requirements and other related disciplines.
  • Understanding of departmental working relationships
     

Function

Manufacturing

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.