1+ months

Process Engineer II (Drug Manufacturing Processes)

Salt Lake City, UT 84111
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!

Job Description

Hands-on engineering position with responsibility for developing drug manufacturing processes, selecting raw material suppliers, producing supplies for clinical trials, and writing documentation for FDA applications. Products are primarily semi-solids and liquids for topical and transdermal drug delivery, including drug/device combination products. Candidate must be self-motivated as this engineer will work under general supervision on a small team.

Essential Duties and Responsibilities
  • Collaborate with formulators to develop small and large scale drug product manufacturing processes
  • Select raw materials and packaging suppliers for pharmaceutical use and maintain specification documents
  • Collaborate with commercial manufacturing groups, including contract manufacturing organizations
  • Participate in design control activites for drug/device combination products
  • Statistical design of experiments and process control
  • Prepare varous documents, including specifications, manufacturing batch records, technical reports, SOPs and FDA applications
  • Coordinate, supervise and participate in manufacturing of batche for use in clinical and stability studies
  • Work within a cGMP quality system
  • Conduct investigations into manufacturing problems and implement corrective and preventive actions
  • Perform risk assessments for manufacturing processes, formulations and device designs
  • Bachelor's degree in engineering or science required
  • 5+ years of experience in laboratories or other technical fields, or an equivalent combination of education and experience required.
  • Time management skills to work on multiple projects simultaneously
  • Excellent communication skills, both written and verbal
  • Strong problem solving skills, especially mechanical, chemical, and logistical
  • Good statistical skills
  • Knowledge of chemistry preferred, experience with aerosols a plus.
  • Ability to work in a manufacturing environment with hazardous materials and industrial equipment
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.


Posted: 2019-09-30 Expires: 2019-11-23

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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Process Engineer II (Drug Manufacturing Processes)

Teva Pharmaceuticals
Salt Lake City, UT 84111

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