1+ months

Process Engineer

Davie, FL 33314
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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 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

 

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we have 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

  • Innovate, optimize and troubleshoot commercial manufacturing processes throughout lifecycle to improve process/product robustness, reduce cost and eliminate waste in oral solid dosage manufacturing of modified release products using conventional and novel technologies.
  • Design, develop and optimize process simulation techniques for process optimization and scale up.
  • Providing process engineering expertise for technology transfer, from pre-validation through commercial lifecycle for modified release solid oral dosage form manufacturing including scale up, validation and lifecycle changes
  • Perform technical analysis to understand and reduce technology transfer risk, estimate cycle time, improve equipment fit, and implement required technologies
  • Provide continued technical leadership to commercial operations and ensure cost effective and robust manufacturing processes for various unit operations including blending, sizing, compression, coating, fluid bed processing, and novel technologies.
  • Maintain product during lifecycle (stage 3 CPV) using appropriate statistical tools 
  • Implement and lead use of new pharmaceutical manufacturing technologies including melt extrusion, spray drying, extrusion spheronization, spray congealing, laser drills, nano particulates, continuous manufacturing, NIR, PAT, etc
  • Lead and execute material changes, process changes, cost reduction projects and CPV

Qualifications

  • Master of Science or PhD degree in Chemistry, Pharmaceutical Engineering, Pharmaceutical Manufacturing, or Pharmaceutical Technology is required
  • Proficiency with statistics (using JMP or Minitab), SPC, NIR, PAT and project management is necessary
  • Experience using Excel for data mining and analysis is required
  • Experience with novel manufacturing technologies (at least two) melt extrusion, extrusion spheronization, spray drying, spray congealing, laser drills, nano particulates, continuous manufacturing, NIR or PAT
  • Minimum 7 years experience; out of which at least 3 years in modified release oral solids manufacturing
  • Excellent verbal, written, and interpersonal skills required
  • Understanding of various unit operations used in conventional and novel oral solid dosage manufacturing
  • Comply with FDA regulations at all times
  • Skill levels in MS Office including proficiency in Word, PowerPoint, Excel and SharePoint
  • Must be able to maintain the highest levels of confidentiality, integrity and discretion

Function

Manufacturing

Sub Function

Technical Transfer

Reports To

Senior Director MS&T

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 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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to  support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. 

Posted: 2021-03-16 Expires: 2021-06-12

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

Teva Pharmaceuticals
Davie, FL 33314

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