1+ months

Quality Analyst II

Cincinnati, OH 45202
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 Cincinnati production site is one of our solid manufacturing and supply chain operations.

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 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 Quality Analyst II to join our team in Cincinnati, OH!  As a Quality Analyst I you will be responsible for reviewing documentation for batches that are manufactured and packaged, and assure compliance with cGMP before being released for further processing, packaging or commercial market.

 

The hours for this position are Monday Thursday from 6:30am 4:30 pm.

 

You will:

  • Review completed manufacturing and packaging documents and laboratory test specification sheets.
  • Ensure timely releases of bulk product and cGMP compliance of the facility.
  • Ensure all pertinent information is compiled, reviewed and approved prior to any product disposition
  • Identify improvements/new procedures/ compliance gaps based on applicable regulations.
  • Assign QA status (Release/Reject/Quarantine/Impound) to work-in-process and finished product.
  • Investigate and troubleshoot all routine problems that occur during work assignments.
  • Coordinate all necessary paperwork for batch release.
Qualifications
  • 4-year Bachelors Degree in Science-related strongly preferred. (Additional GMP Quality experience may be accepted in lieu of degree).
  • 3+ years experience within heavily regulated (GMP) manufacturing facility required. Pharmaceutical experience preferred.
  • Thorough understanding of cGMPs.
  • Ability to perform basic statistics and understand AQL sampling plans
  • Computer literate, ability to work with MS Office and software programs related to the position.
  • Ability to read, understand and follow instructions written in English for SOPs, batch records, cGMPs, etc.
  • Ability to communicate clearly and concisely when conveying information, summarizing facts, asking questions, etc.
  • Experience working with cross-functional groups such as planning, manufacturing, packaging, and distribution to ensure proper priorities are set and necessary activities are planned to meet these goals.
  • This role may require standing for long periods of time, walking around the facility, and lifting up to 25 lbs.
Function
Quality
Sub Function
Manufacturing Quality Assurance
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.

Categories

Posted: 2020-11-23 Expires: 2021-02-10

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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Quality Analyst II

Teva Pharmaceuticals
Cincinnati, OH 45202

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