1+ months

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 Control Auditor II to join our team in Cincinnati!

 

As a QC Auditor, you will ensure that equipment, solutions, and methods used in the Quality Control Laboratory meet all acceptance criteria and that lab notebooks and related documentation are accurate.

 

You Will:

 

  • Perform routine and non-routine audit of chemical testing documentation for commercial, validation and stability samples in accordance to written methodology.
  • Experience utilizing electronic laboratory information systems such as LIMS and Empower to perform the electronic review of analytical data.
  • Audit Analyst notebooks to ensure the following: Test methods were correctly followed; Verify data against approved specifications, notifying management of any OOS and aberrant results; Ensure that the equipment used during an analysis was within the calibration date; Verify the integrity and expiration date of solutions used to prepare samples.
  • Review lab record documentation (notebooks and computer based) according to GMPs.
  • Demonstrate the philosophy of Right First Time.
  • Maintain a clean and safe work environment and follow safety procedures and policies.
  • Provide feedback on systems and processes to promote continuous improvement and champion selected changes.
  • Grow in the job, accountable for establishing and accomplishing annual personal development goals.
  • Contribute to department and site goals.
  • Communicate clearly and well within a team environment.
  • Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives. Share information with others keeping management informed and helping department to meet the goals.
  • Actively participate in regular one-on-one meetings with direct supervisor.
  • Communicate externally to the department, where applicable.
  • Collaborate effectively to achieve team and organizational goals.
  • Prioritize assigned work to maximize time and equipment efficiency.
  • Work independently with limited supervision for routine assignments.
  • Troubleshoot problems encountered with procedures, methods, and other processes - routinely solve, choosing among clearly defined alternatives.
  • Occasionally solve more complex problems - these may involve less familiar procedures or incomplete information.
  • Provide the accurate, timely and compliant execution of assigned projects, audit of analytical documentation.

Qualifications

  • BS or higher in science related discipline required, chemistry is preferred.
  • Minimum 5 years of experience in a Lab Environment required. Pharmaceutical environment preferred.
  • Auditing or peer review experience is mandatory.
  • Basic knowledge and understanding of USP, cGMP, and FDA regulations strongly preferred.
  • Familiar with the qualitative and quantitative data that is typically generated using analytical instrumentation such as HPLC; GC, UV/Vis, KF and FTIR is a must.

 

Function

Quality

Sub Function

Manufacturing Quality Control

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: 2020-12-02 Expires: 2021-02-13

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.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

QC Auditor II

Teva Pharmaceuticals

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast