7 days old

Quality Control Analyst I - Micro

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 Cinicinnati, Ohio production sites are 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!

Job Description

Teva is searching for a Quality Analyst I to join our team in Cincinnati, OH! As a Quality Analyst I you will be responsible for performing Environmental monitoring of manufacturing environment and critical Utilities (water and gas systems) and Performing Microbiological Examination of Raw materials, finished product, and media growth promotion per USP or applicable internal methods.

You will:

  • Participate in microbial method validation and special projects related to improvement and validation projects.
  • Perform general laboratory duties, in house media preparation, and housekeeping
  • Documentation of data/reports per local procedures and GMP/regulatory requirements and experience with a technical writing is a plus. Knowledge of Aseptic Techniques, GLP, and GMP environment.
  • Works independently and with the team effectively to achieve individual, team and organizational goals
  • Create and maintain lab record documentation (notebooks and computer based) according to GMPs
  • Identify and provide feedback on systems and processes to promote continuous improvement
  • Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives
  • Shares information with others keeping management informed and helping department to meet the goals
  • Actively participate in regular one-on-one meetings with direct supervisor
  • Prioritize assigned work to maximize time and equipment efficiency
  • Occasionally solve more complex problems - these may involve less familiar procedures or incomplete information
  • Limited scope for independent decision making, the greater emphasis is placed on the identification of issues in own role and communicating same to line management.
  • Be responsible for the accurate, timely and compliant execution of work assignments, testing and related documentation


  • Bachelors Degree, with Microbiology or Biology coursework
  • 0-2 years of experience in pharmaceutical or other FDA industry or related field
  • Able to operate basic software like Microsoft Office, LIMS, and EDMS.
  • Ability to wear respiratory equipment (PAPR), as needed.
  • Ability to work occasional overtime and weekends to support business needs
  • Actively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions
  • Ability to cope with a rapidly changing work environment



Sub Function

Manufacturing Quality Control

Reports To

In process of validation

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.


Posted: 2021-04-29 Expires: 2021-06-05

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 Control Analyst I - Micro

Teva Pharmaceuticals

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