
Coordinator, External Quality
- North York, ON
- Permanent
- Full-time
- Coordinate and perform activities related to reconciliation, inspection and disposal of reserve/retain samples for third party products.
- Coordinate, compile and review documentation to support release of third party products.
- Conduct follow-ups, receives/logs and coordinates shipment of complaint samples for third party products.
- Assist in follow up with Third Party Organizations (TPOs) for documentation, protocols/reports, change controls, deviations and other documents required for Product Compliance File (PCF) to support product launch and product/batch disposition.
- Interacts with external TPOs and internal functional groups for obtaining the required documentation to support product launch and product disposition.
- Organizes the management of the departmental controlled documents.
- Create and perform follow-up on change control records dealing with third party products and departmental controlled documents.
- Participate in creation and updating of departmental procedures.
- Participate and provide support in compilation of data/information to support departmental objectives/projects.
- Performs all work in accordance with all established procedures, regulatory and compliance and safety requirements.
- Performs all work in support of Apotex's Values of Collaboration, Courage, Perseverance and Passion.
- Works as a member of a team to achieve all outcomes.
- Other duties as assigned.
- Education
- Post-secondary education in Business or Science, Administrative or equivalent work-related experience preferred.
- Knowledge, Skills and Abilities
- Effective in communicating (speak, read and write) in English
- Excellent organizational skills and the ability to manage time effectively
- Strong interpersonal skills and very customer focussed
- Must be detail-oriented, accurate and reliable
- Must be able to work independently with minimal supervision
- Ability to follow instructions according to written procedures
- Ability to manage multiple priorities in a fast-paced and changing environment
- Knowledge of GMP and regulatory requirements
- Familiarity with MS Word, Excel and Access is an asset
- Experience
- Three to five years of experience in a pharmaceutical environment