Trainee, Gbs-emq

**About Apotex Inc.**

Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products.

**Job Summary**:
Responsible for managing the Quality Product Compliance files for Canada and the U.S. Additionally, acts as the primary Quality contact for products which Apotex acts as a contract manufacturer.
Acts as liaison between Apotex’s manufacturing sites and customer affiliates.

**Responsibilities**:

- Maintain Quality Product Compliance files for all 3rd party contract manufactured product in which Apotex is the Marketing Authorization holder or acts as a distributor for the Canadian market; this includes formally requesting annually with our vendors their current approved master documentation, stability summary reports. Follows up with vendors to ensure all documents are received.
- Develops and maintains Quality Product Compliance files for the US marketplace based on current GMP Regulations.
- Perform assigned Post implementation tasks from TrackWise.
- Initiate the Change Controls in TrackWise, where no RA assessment required.
- Tracking of confirmatory testing & batch record review (Initial launch batches and annual batches).
- Request and obtain vendor APRs as per the schedule on time.
- Maintain and track unique identifier documentation and expiry and ensure up to date.
- Acts as the liaison between external customers and our internal functional groups to provide customer quality requests in a timely manner.
- Interacts with internal functional groups including stability, quality assurance, quality control, regulatory affairs, and quality compliance for obtaining the necessary documentation and handling customer requests.
- Tracks open requests from customers to ensure timely responses. Escalate to senior management any significant delays.
- Responsible for timely compilation of batch release documents under guidance of Global External Manufacturing Quality.
- Responsible for timely updation of batch release tracker associated with batch release activity.
- Coordinate with third party manufacturing sites and internal stakeholders for obtaining required documents for release of batches in US and Canada market.
- Escalate any non-conformance/delay associated with batch release documents compilation to Global Batch Release team.
- Assist External Manufacturing Quality with follow up for new product launch, change control or deviations.
- Performs all work in accordance with all established regulatory and compliance and safety requirements.
- Works in a safe manner collaborating as a team member to achieve all outcomes.
- Demonstrate Behaviors that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
- Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- All other relevant duties as assigned.

**Job Requirements**:

- **Education** Bachelor of Science Degree/Community College Diploma (or equivalent) in a related discipline.
- **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 focused.
- Must be detail-oriented, accurate and reliable.
- Must be able to work independently with mínimal 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.- **Experience**
- One to two years of experience in a pharmaceutical environment.
- Familiarity with MS Word, Excel and Access is an asset.

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.