1+ months

Quality Control Analyst (Method Transfer)

Cincinnati, OH 45202
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 QC Analyst II to join our team in Cincinnati, OH!

 

As a QC Analyst II you will actively participate as a team member supporting the routine and non-routine testing of drug products and raw materials into the QC Laboratory.  The Analyst performs analytical bench chemistry according to established compendia and vendor specifications.  The ideal candidate will have strong problem solving and analytical capabilities and must be able to work independently to achieve team goals and milestones.

 

You will:

  • Perform analyses and tests of drug products, raw materials, in-process materials, release test samples or stability samples, packaging materials, quantitative assays on samples, and/or finished products from manufacturing, to ensure quality standards and compliance with established specifications
  • Perform a variety of qualitative tests or qualitative assays on samples using techniques that vary from standard analytical equipment to modern and automated instrumentation. 
  • Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data 
  • Be responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation
  • Serve as a mentor for more junior analysts within the team providing guidance and direction as needed
  • Stay current on new requirements & making associated recommendations that affect area of expertise.
  • Use risk assessment tools within your own area using knowledge, managing risk and assessing impact to make decisions
  • Promote Quality and GMP by analyzing the implications of deviations, and implement solutions under guidance.
  • 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
  • Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives 
  • Actively participate in regular one-on-one meetings with direct supervisor
  • Troubleshoot problems encountered with methods and instruments - routinely solve, choosing among clearly defined alternatives
  • Applies root cause problem solving principles for identification and implementation of effective corrective and preventive actions
Qualifications
  • BS or higher in science related discipline, chemistry is preferred
  • 5 years of Quality Control experience required.
  • Minimum 2 years of experience in a pharmaceutical environment required.
  • The position requires ability to run and trouble-shoot new chromatographic procedures.
  • 2+ years of experience with HPLC and UPLC required.
  • Thorough knowledge and understanding of USP, cGMP, ICH and FDA guidelines required. Experience with raw material testing for USP Monograph <401> Fats and Fixed Oils, and related testing is preferred.
  • Ability to independently solve analytical problems and view from new perspective using existing solutions required.
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: 2020-06-04 Expires: 2020-07-09

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 (Method Transfer)

Teva Pharmaceuticals
Cincinnati, OH 45202

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