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Teva Pharmaceuticals Analytical Chemist II - 1 year contract in Toronto, Ontario

Analytical Chemist II - 1 year contract

Date: Jan 14, 2022

Location: Toronto, Ontario, CA, M1B2K9

Company: Teva Pharmaceuticals

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

The Quality Control Laboratory Analytical Chemist II is responsible to work independently with minimal or no supervision under the direction of the QC Manager/Chemist 5 performing analytical testing dealing with moderately complex chemical and physical analyses associated with commercial production and stability samples. As an Analytical Chemist 2, responsibilities also extend to providing technical and analytical support when necessary to the QC Laboratory.

Tasks and responsibilities will include but are not limited to:

  • Performs analytical testing of materials associated with commercial production and stability samples.

  • Assists with the execution and completion of analytical investigations carried out by QC Laboratory as required.

  • Assists in the new technology implementation as required.

  • Performs all planning functions that are integral to the overall operation of the laboratory and in so doing, ensures that execution of work can be carried out in most cost effective and productive manner.

  • Performs all QC project management activities associated with new product launches, alternate sourcing, site transfer and, other company initiatives as they relate to cost savings and continuous improvement.

  • Performs other related duties as required

Qualifications

  • College Diploma or University Degree in Chemistry or a related science.

  • 2+ Years Laboratory Experience

  • LIMS (Laboratory Information Management System), CDS (Chromatography Data System), Trackwise, MSOffice, Oracle, SQC (SmartQC)

  • Knowledge of, and experience in a Quality Control Laboratory and working knowledge of GMP/cGMP as they pertain to QC laboratory unit.

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

Manager Quality Control Laboratory

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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)

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.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

EOE including disability/veteran

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