The opportunity
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! This Co-Op position would be assigned to the Manufacturing Science & Technology (MS&T) group working with Validation Engineers in designing, planning, and implementing validation projects in an FDA regulated cGMP pharmaceutical/medical device manufacturing plant. This individual will work with cross functional teams such as R&D, Engineering, Operations, and Quality in launching women’s hormonal products improving patient’s health.
How you’ll spend your day
Essential Duties & Responsibilities
· Work closely with the validation staff to become familiarized with applicable codes and standards in the pharmaceutical and medical device industries.
· Implement validation projects supporting the validation team
· Work with Engineers to present project proposal, justification, timeline and status to cross-functional teams and site management.
· Work with Engineers, R&D, and other sites to transfer new products to the facility
· Work with Engineers to identify and develop solutions to improving existing manufacturing processes.
· Write Protocols and Reports supporting Process Validation, Packaging Validation, and Cleaning Validation
· Use statistical software under validation engineer’s guidance.
· Contribute to continuous improvement and participate on teams to understand current and future states for better quality, safety, compliance, and efficiency outcomes.
