Stability Associate – 12 month contract
Date: Mar 7, 2023
Location:
Toronto, Ontario, Canada, M1B2K9
Company: Teva Pharmaceuticals
Job Id: 46066
Who are we?
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
Working independently under the supervision of the Stability Supervisor, the incumbent having a solid knowledge of statistic concepts, analytical chemistry, and regulatory stability requirements, administers and coordinates activities associated with Teva Canada Stability Programs in a timely, cost-effective, and compliant manner.
Tasks and responsibilities include but are not limited to:
Execute and coordinate the activities of the Teva Canada QC Stability Program by GMPs, cGMP, and standard operating procedures. Ensure stability requirements for various markets are met and programs are administered compliantly. Receives and processes all the stability samples in the Quality Control Laboratory.
Execute the stability program with QC Planners to ensure all samples are tested compliantly.
Maintain the offshoring stability program.
Support the completion of Annual Product Reviews.
Support QA in product release, third-party markets, and private label business.
Qualifications
Minimum College Diploma in Chemistry or Related Science Discipline
Minimum (3) years of chemistry lab experience in applied statistics, preferably in a chemistry lab environment.
In-depth knowledge of technical requirements for USP/NF, BP/EP, in-house methods, and general laboratory procedures. Good understanding of GMP/cGMP regulations as they apply to laboratories—knowledge of analytical instrumentation.
LIMS (Laboratory Information Management System), MSOffice, Oracle, SmartQC, Statistical software applications / LIMS statistical functions
In-depth knowledge of, and experience with, ICH guidelines GMP/cGMP about laboratories.
Good knowledge of RA / QA business processes
Good knowledge of the business process of laboratory and Quality / Compliance departments
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 (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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