MS&T Co Op

Teva Pharmaceuticals • Cincinnati, OH

6d • Onsite

About The Position

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.

Requirements

• Applicants must be currently enrolled in an accredited college or university program preferably pursuing a chemical, mechanical, or biomedical engineering degree (other majors will be considered)
• Strong interpersonal and communication skills will be required to engage with other departments within the site.
• Strong time management skills.
• Proficient in Microsoft Office programs
• Works independently and receives minimal guidance.

Nice To Haves

• Previous Co-Op experience preferred, but not required

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level