1+ months

Process Engineer

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!

 

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

Job Description

This position will focus on managing the validation processes within site operations in order to facilitate successful on-time productlaunches and lifecycle events (including various pre-requisites and post validation commitments).
Lead and assist project teams responsible for PQ of equipment, pre-validation, validation, CPV and cleaning validation
Author, execute or review or approve documentation for validation (PV and CV)
Create and lead project tracking systems
Lead and support risk management processes for product and processes
Author, review or approve (as needed) investigation reports, protocols batch records and CMC documentation
Knowledge and experience in use of various solid oral dosage manufacturing and packaging technologies Knowledge of current
and advanced validation strategies using statistics, current regulatory landscape and agency expectatio

Qualifications

A Master of Science or PhD degree in Chemistry, Pharmaceutical Engineering, Pharmaceutical Manufacturing, orPharmaceutical Technology is required
Proficiency with statistics (use of Minitab or JMP), NIR and project management tools is required
Experience using Excel for data mining and analysis is required
Experience with novel manufacturing technologies (minimum two) melt extrusion, spray drying, spray congealing, extrusionspheronization, laser drills, nano particulates, continuous manufacturing, NIR or PAT
Minimum 3 years experience in validation of oral solid dosage forms including risk management
Excellent verbal, written, and interpersonal skills required
Work with minimal supervision
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

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 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. 

Categories

Posted: 2021-02-05 Expires: 2021-04-25

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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