Apotex is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines (both generic and innovative pharmaceuticals) for patients around the world.
We are the 7th largest generic pharmaceutical company globally with more than 12,000 employees and estimated sales of approximately $3 billion.
Our fully integrated operation is comprised of four lines of business : Global Generics; Apobiologix; Global Active Pharmaceutical Ingredients (API);
and ApoPharma (Innovative Products). With our worldwide manufacturing sites, Apotex can produce up to 24 billion dosages per year.
We produce 300 medicines in 4,000 dosages and formats that are exported to 115 countries. Apotex will spend $2 billion over the next 10 years on research and development.
Responsible for ensuring root cause analysis is conducted on investigations for Apotex OSD in a timely and efficient manner.
Ensures established procedures are followed for all investigations and corrective and preventative actions are implemented.
Acts as quality technical resource and reviews all investigation reports for completeness and acccuracy, and compliance.
Conducts all Apotex OSD failures or deviations (product, validation, stability, process and procedures) and ensures investigations are initiated following existing procedure.
Conducts investigations for product failures or deviations for both Signet and Etobicoke sites following existing procedures.
Recognize critical path for investigations leading to timely identification of root cause, corrective & preventative actions.
Writes product failure investigation reports for approval by Department Manager.
Notify appropriate Team Leaders of validation, raw material, stability & in-process failures and ensure investigations are initiated and completed as per existing procedure.
Act as quality technical resource and provide support & guidance to groups within Operations.
Ensure identification of most probable root cause, corrective action & preventative action for all completed investigations.
Review all investigation reports for completeness and accuracy prior to approval by Department Manager.
Conduct impact analysis of proposed corrective & preventative actions. Discuss findings with impacted departments (QA, RA, Validation, Production, ect) and prepare recommendations for Department Managers.
Prepare and maintain list of open investigation for Apotex OSD Management.
Review on-going progress on all open investigations with Project Leaders and Coordinators.
Ensure investigations are issued; tasks are appropriately assigned for completion or corrective and preventative actions and are closed in a timely fashion.
Project manages the corrective and preventative actions and assists in both implementation and follow-up.
Bachelors degree in science
5-7 years’ experience in the pharmaceutical industry, preferably in Quality Engineering or QA / QC role.
Experience in project management
Fluency in project management & RCCA tools
Superior organizational, interpersonal communication skills
Ability to manage time effectively
Ability to work independently and manage multiple priorities in a fast-paced and changing environment
Good command of the English language, both written and verbal
Knowledge of GMP
Proficiency with Word, Excel, and SAP.
At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported.
Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.