27 days old

Chemical Process Engineer

Davie, FL 33314
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

    Lead and execute lifecycle activities from start to end for modified release solid oral dosage form manufacturing including scale up, validation and lifecycle changes.
    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
    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.
    Author, review and/or 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, extrusion spheronization, spray congealing, laser drills, nano particulates, continuous manufacturing, NIR, PAT, etc.
    Lead and execute material changes, process changes and cost reduction projects
    Provide technical training and assistance to others

Qualifications
  • A Bachelors or Masters in Chemical or Pharmaceutical Engineering, Pharmaceutical Manufacturing, or Pharmaceutical Technology is required
  • Proficiency with statistics (using JMP or Minitab), SPC, NIR and project management is a must
  • Experience using Excel for data mining and analysis is must
  • 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.
  • Min 3 years experience in modified release oral solids manufacturing
Function
Manufacturing
Sub Function
Technical Transfer
Reports To

Sr Dir 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.

Categories

Posted: 2020-07-14 Expires: 2020-08-14

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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Chemical Process Engineer

Teva Pharmaceuticals
Davie, FL 33314

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