Quality Control Analytical Chemist I - Eurofins CDMO Alphora, Inc. job opportunity at Eurofins.

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Date2026-05-01T19:46:07.576Z bot
Eurofins Quality Control Analytical Chemist I - Eurofins CDMO Alphora, Inc.
Experience: General
Pattern: Full-time
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Inc.

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degreeGeneral
loacation Oakville, Ontario, Canada
loacation Oakville, Onta..........Canada
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Job DescriptionEurofins CDMO Alphora is looking for a dynamic Quality Control Analytical Chemist to join our Team! The ideal candidate will:possess a high degree of initiativeis a team player with excellent communication abilitiesis comfortable in a modern, state of the art laboratoryhas practical experience with HPLC, GC, KF and various wet chemistry techniqueshas a strong attention to detail and a comprehensive understanding of cGMPhas strong organizational skills with the ability to multitask and work in a fast-paced environmentOur Quality Control department plays a key role in ensuring Eurofins CDMO Alphora Inc.’s compliance with Current Good Manufacturing Practices (cGMP) to ensure the production of safe and efficacious pharmaceutical APIs on behalf of our clients and their patients. The Quality Department is responsible for providing analytical support for the API manufacturing plant including support of raw material and finished product release, in process control testing, cleaning verification and other investigations.You will be working collaboratively with a small, dedicated team of QC chemists. Teamwork, communication and individual responsibility are key requirements. This is an excellent opportunity to obtain experience in a pharmaceutical manufacturing setting and to work on projects related to all phases of the pharmaceutical product life cycle.Responsibilities include but are not limited to:Testing of raw materials, in process controls, intermediates and finished products in support of our cGMP manufacturing operations.Interpret and report all test results, tabulate data and generate reports as required.Responsible to identify OOS results and assist in their investigation.Assist in maintaining the lab in a state of compliance by performing calibration checks and performance verifications of laboratory equipment.Work in accordance with established cGMP and safety requirements.Perform other related duties as required.

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