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Teva Pharmaceuticals Senior Quality Associate (1st shift) in Cincinnati, Ohio

Senior Quality Associate (1st shift)

Date: Oct 15, 2020

Location: Cincinnati, Ohio, US, 45213

Company: Teva Pharmaceuticals

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!

Job Description

Teva is searching for a Sr. QA associate, Quality to join our team in Cincinnati, OH!

As a Sr. QA associate Quality, you will be responsible for being the quality team member on new product initiatives and supporting daily plant operation. Functions include deviation writing/approval, documentation reviews, and validation review/support.

Current Hours: Monday through Friday 8am – 5pm

You will:

  • Be the Quality team member for technical transfer and R&D product teams.

  • Communicate directly with the Manufacturing and Packaging Supervisors throughout the shift to assist in problem solving while providing quality requirements.

  • Identify improvements/new procedures/ compliance gaps based on applicable regulations.

  • Complete and document manufacturing/packaging deviation reports. Ensure all pertinent information is compiled, reviewed and approved prior to any product disposition.

  • Work with Operations to investigate and troubleshoot all routine problems occurring during work assignments.

  • Approve Change controls, review/approve SOPs, and Review/approve specifications, batch records, and qualification documents.


  • 4-year Bachelor’s Degree within a scientific discipline strongly desired.

  • Minimum 5 years of experience in Quality within a pharmaceutical, food, nutraceutical or related manufacturing environment required.

  • Thorough knowledge of cGMP’s required.

  • Working knowledge of US and European Drug Product GMP requirements and associated guidelines with ability to increase others knowledge preferred.

  • Experience in administration of quality systems for drug product development, manufacturing and quality assurance operations required.

  • Ability to make independent decisions and take appropriate actions required.

  • Knowledge of MS Office, including Word and Excel required. SAP preferred.

  • Ability to read, understand and follow written instructions such as SOPs, batch records, cGMPs, etc.

  • Ability to be clear and concise when conveying information, summarizing facts, asking questions, etc.

  • Must effectively work with different departments and communicate with all levels of management.

  • Ability to coordinate several activities at once while ensuring on time releases of finished products.

  • Must work with planning, manufacturing, packaging, and distribution to ensure proper priorities are set and necessary activities are planned to meet these goals.



Sub Function

Manufacturing Quality Assurance

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Teva’s 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.

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