AddressAbout Apotex Inc.
Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations. Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India. Through vertical integration, Apotex is comprised of multiple divisions and affiliates including Apotex Inc., focused on generics; Apobiologix, a division of Apotex Inc. focused on biosimilar development; Aveva, an affiliate of Apotex Inc. fully integrated global developer and manufacturer of complete transdermal solutions; Apotex Consumer Products, a division of Apotex Inc. focused on brand name products; and Global Active Pharmaceutical Ingredients (GAPI), a division of Apotex Inc. focused on the manufacturing of active pharmaceutical ingredients (API) for Apotex and third parties. For more information visit: www.apotex.com.
Job Summary
Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation.
Job Responsibilities
- To ensure timely completion of analysis and data completion for the same.
- To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems.
- To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and cleaning validation.
- To Prepare Stability Trend Reports for Laboratory samples.
- To collect and maintain various laboratory samples.
- To generate and maintain records related to laboratory samples.
- Works as a member of a team to achieve all outcomes.
- Performs all work in accordance with all established regulatory and compliance and safety requirements.
- Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
- To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory.
- 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 duties as assigned.
Job Requirements
- Education
- M.Sc\BPham or any equivalent degree
- Knowledge, Skills and Abilities
- Effective command over verbal and written communication with good interpersonal skills.
- Command on Microsoft-Office (Word, Excel).
- Able to prioritize the tasks.
- Best in effective planning of work activities to meet the time lines.
- Experience
- Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.
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.
