1+ months

Validation Engineer

Davie, FL 33314
Apply Now
Apply on the Company Site
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


  • Provide assistance in troubleshooting to manufacturing and packaging areas
  • Interface with Quality Assurance and Research and Development (R&D) on process requirements for new and current products
  • Work in conjunction with maintenance department to identify, recommend and implement the upgrade of current equipment and the purchase of new equipment within regulatory requirements
  • Analyze new and existing equipment, recommends equipment modifications as needed for validation optimization
  • Perform studies to support necessary equipment and system IQ, OQ, and PQ's to assure compliance in all manufacturing and support areas
  • Assist with on-site transfer projects and product scale-up activities
  • Recommend improvements in manufacturing and control systems
  • Review mechanical, specifications in manufacturer and blue print form, and identify critical parameters
  • Analyze statistical data, product or functional specifications to determine conformance with standards and established quality requirements.
  • Review and approve protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment
  • Assure that protocols are approved through proper channels. Write and revise validation protocols.
  • Execute validation protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
  • Analyze data to ascertain if it meets related protocol acceptance criteria; writes deviation reports 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
  • Provide timely updates to management on the status of various projects
  • Provide technical training and assistance to others
  • Bachelors degree from an accredited college or university
  • Minimum of 3 years  pharmaceutical formulation or pharmaceutical process development or pharmaceutical pre-validation experience
  • Experience preparing all types of pharmaceutical and regulatory documentation (e.g., BR, BOM, CC, protocols, summary reports, evaluation reports) 
Sub Function
Technical Transfer
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: 2020-05-18 Expires: 2020-10-24

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.

  • Salary Questions

    Find out how your paycheck compares by industry, function, location, and more.

    Check Right Now

  • Tips for ABLE Grads

    From creating the perfect resume to nailing the interview, this article is a must-read before you start your Job Hunt.

    Get Started Now

  • Set Up Your Job Alerts

    Be alerted when a job is posted that fits your professional criteria.

    Set Up Your Alerts Right Now

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Validation Engineer

Teva Pharmaceuticals
Davie, FL 33314

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast