1+ months

Process Engineer -- MSAT

Davie, FL 33314
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!


Tevas Davie and Sunrise (Florida) production sites are two of our largest launch facilities.   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. For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com




Job Description


As a Process Engineer, we will count on you to:


  •  Lead and execute lifecycle activities from start to end for solid oral dosage form manufacturing (including manufacturing and packaging areas) including scale up, validation and lifecycle changes
  •  Interface with various internal and external stakeholders for process requirements for new and current products
  •  Work in conjunction with maintenance department to identify, recommend and implement r upgrade of current equipment or the purchase of new equipment within regulatory requirements
  •  Lead documentation for equipment, lead FMEAs, recommend equipment modifications as needed for validation optimization, Analyze statistical data from qualification, product or functional specifications to determine conformance with standards and established quality requirements.
  •  Perform studies to support necessary equipment and system PQ's and PPQs to assure compliance in all manufacturing and support areas, analyze data using appropriate statistical tools
  •  Maintain product during lifecycle (stage 3 CPV) using appropriate statistical tools
  •  Assist with on-site transfer projects and product scale-up activities
  •  Recommend improvements in manufacturing and control systems
  •  Review and approve protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment
  •  Write and execute experimental and validation protocols as per related SOPs and assure that acceptance criterion related to experimental, validation and qualification protocols are met.
  •  Lead investigations, write investigation reports with appropriate scientific understanding, as required upon failures to meet protocol acceptance criteria.
  •  Write final reports and assure that they are approved through proper channels
  •  Coordinate resources from Engineering, Research and Development, Technical Services, Quality Assurance and production personnel assigned to specific projects. Furnish direction to engineers and technicians with regard to project requirements. Develop and communicates project timelines and status
  •  Review and critique investigation reports, protocols batch records and CMC documentation
  •  Lead projects by use of appropriate project management tools, provide timely updates to management on the status of various projects
  • Implement and lead use of new pharmaceutical manufacturing technologies including melt extrusion, spray drying, spray congealing, laser drills, nano particulates, continuous manufacturing, PAT, etc.
  •  Lead and execute material changes and cost reduction projects
  •  Lead and support regulatory and internal audits for relevant topics
  •  Provide technical training and assistance to others


  • Master of Science (MS) or PhD degree in Chemistry, Pharmaceutical Engineering, Pharmaceutical Manufacturing, or Pharmaceutical Technology  is required
  • Minimum  2 years  experience with at least two of the following new technologies:  melt extrusion, spray drying, spray congealing, laser drills, nano particulates, continuous manufacturing, or PAT
  • Proficiency with statistics, NIR and project management is a must
  • Experience using Excel for data mining and analysis is must
Sub Function
Technical Transfer
Reports To

Senior Director, Manufacturing Science and Technology (MSAT)

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: 2019-12-20 Expires: 2020-02-08

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 -- MSAT

Teva Pharmaceuticals
Davie, FL 33314

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