Contracts Associate

2 weeks ago

Toronto, Ontario, Canada Tevapharm Full time
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Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives.

Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List.

Today, at least 200 million people around the world take one of our medicines every single day. Quality Assurance Associate - 6 month contract

The Quality Assurance Associate will provide support to operations by providing oversight to activities associated with the manufacturing and packaging of bulk and finished products by third party suppliers to ensure compliance with GMPs.

Review & approve GMP documentation associated with 3rd party supplied bulk & finished products including release documentation, deviations, validations, change controls, etc.

Liaise with 3rd party suppliers to ensure compliance with GMPs, adherence to Quality agreements & to resolve quality issues
Investigate Product Complaints and ensure the timely closure of the records in Harmony Trackwise
Perform comprehensive and detailed investigations for quality deviations (DR's) related to 3rd party products in a timely manner
Follow up and facilitate the completion of change controls, DRs, CAPAs and CAPAERs in a timely manner
Request stability data from the suppliers and perform stability review for all the third party products;
Draft / revise, negotiate and execute Quality Agreements with manufacturing sites, contract packagers, contract laboratories, etc.
Review internal procedures and Corporate Standards, perform gap assessment and update SOPs accordingly

Perform retain sampling activities:
conduct the receipt of retain samples, updating of Oracle / storage of retain samples and destruction of expired retain samples as per procedures
Support other Compliance functions and projects as required
Lead / Manage special projects that require collaboration with cross-functional teams and Teva Global Affiliates
Perform incident/accident investigations, root cause analysis, and establish appropriate corrective actions.

Role Modeling:
Role modelling of EHS practices to prevent the release of materials/energy, reduce EHS impacts, and ensure adherence to EHS regulatory requirements and procedures
Must have a minimum of 1 (one) year relevant experience in Quality Control, Quality Assurance
~3 (three) + years relevant experience in Quality Control, Quality Assurance or a proven track record within pharmaceuticals is preferred.
~ If you are a current Teva employee, please apply using the internal career site available on "Employee Central". 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.

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.

All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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