1+ months

Manager, Manufacturing Science and Technology (MS&T)

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!

 

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!

Job Description

As a Manager, MS&T, we will count on you to:

  • 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
Qualifications

 

Education/Experience:

 

  • 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) 

 

Function
Manufacturing
Sub Function
Technical Transfer
Reports To

Senior Director, Manufacturing Science and Technology (MS&T)

Tevas Equal Employment Opportunity Commitment
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.

Categories

Posted: 2019-10-03 Expires: 2019-12-01

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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Manager, Manufacturing Science and Technology (MS&T)

Teva Pharmaceuticals
Davie, FL 33314

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