25 days old

Group Leader Quality Control - 1311

Cincinnati, OH 45202
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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

As a Quality Control Group Leader you will:

  • Schedule/plan laboratory testing and assign work to maximize effectiveness and reduce cycle time; monitor process, progress, and metrics, and design feedback loops into work.
  • Ensure all testing is conducted according to cGMP and compendial requirements

  • Identify and evaluate opportunities for continuous improvement
  • Assess any analytical or instrumental problems, coach and mentor staff to investigate and resolve by determining the root cause and implementing preventative actions.
  • Demonstrate flexibility in adapting to changing business needs.
  • Troubleshoot instrumental analyses using HPLC, GC, UV/VIS, and FTIR as required.
  • Incorporate communication plan with reports into MILO, including but not limited to monthly one on ones, staff meetings, and floor time (i.e., GEMBA, BOS, etc.).
  • Identify goals in the current performance and reward system that will aid in the development of their staff. Monitor and track status of goals and other development activities

 

Qualifications

Requirements:

  • BS in chemistry or related quantitative scientific discipline
  • Min 7 years progressive pharmaceutical QC laboratory experience including Raw material testing and release
  • Excellent knowledge of cGMPs and their application to a pharmaceutical QC laboratory; thorough knowledge of compendia USP, EP, and ICH guidelines.
  • Excellent knowledge of analytical instrumentation theory/practice and wet chemistry techniques
  • Knowledge of MS Office applications and LIMS
  • Technical writing skills, including technical and deviation reports, and investigations; change controls, SOPs
  • Ability to communicate clearly, verbally and in writing, both within and between departments, and to outside clients.
  • Ability to motivate a diverse group of individuals to deliver maximum performance
  • Ability to assign work to staff to meet overall departmental goals with the flexibility to respond to urgent business needs
  • Excellent ability to identify and troubleshoot any analytical problems (methods, instruments, computer applications, general chemistry)

Function

Quality

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: 2020-12-30 Expires: 2021-01-29

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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Group Leader Quality Control - 1311

Teva Pharmaceuticals
Cincinnati, OH 45202

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