Quality Control Analytical Chemist II - Eurofins CDMO Alphora - Jobs in Oakville, ON

Job Description

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 58,000 staff across a network of more than 1,000 independent companies in over 54 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.In 2021, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.________________________________________________________________________Eurofins CDMO Alphora Inc. provides a fully integrated suite of services to support drug substance and drug product development from the IND enabling development stage, through to phase II & III supply, and commercial validation and manufacturing for niche APIs. In addition to a continuing flow of interesting and challenging projects for global pharmaceutical and biotech companies, Eurofins CDMO Alphora Inc. is committed to growing its state-of-the-art organization, with continued investments in its people, modern facilities, equipment, and instrumentation.Job DescriptionYou possess a high degree of initiative and are a team player with excellent communication abilities. You are comfortable in a modern, state of the art laboratory and are proficient with HPLC, GC, KF and various wet chemistry techniques. Your attention to detail, a comprehensive understanding of cGMP, strong organizational skills with the ability to multitask and work in a fast-paced environment, make you the ideal candidate to become a member of our team.Description of Department:The 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.Description of Major Job Responsibilities: Reporting to the Quality Control Supervisor.Responsibilities include but are not limited to:

• Testing of raw materials, in process controls, and final products in support of our cGMP manufacturing operations.
• Coordination of testing priority with operation staff and QC supervisor, review and reporting of results.
• Troubleshooting analytical and instrument performance issues as required.
• Responsible to identify OOS results and assist in their investigation.
• Performing calibration checks and performance verifications of laboratory equipment.
• Work neatly to maintain the laboratory in an organized state.
• Participate in general upkeep and maintenance of the laboratory.
• Perform other related duties as required.

Instrumentation:

• HPLC, GC, GC/Headspace, IR, KF and wet chemistry techniques are core to the role, practical experience with these techniques is a requirement.
• Experience with GCMS, LCMS, Ion Chromatography or other techniques is an asset.

QualificationsQualifications

• Diploma or degree in a related field (Chemistry is preferred) with a minimum of 3 years relevant experience in analytical laboratory analysis, preferably in a pharmaceutical or other regulated environment.
• Excellent documentation and communication skills.
• Excellent problem-solving, planning, and organizational skilled coupled with a strong attention to detail.
• Ability to work independently under minimal supervision.

Additional Information

• This position is based in a laboratory environment; significant time spent standing at a bench or sitting in front of a computer is required.
• Lab supports a 24/5 operating plant. The ability to work rotating shifts is a requirement.
• Extra hours, weekends may be required. Shift and OT premiums are provided.
• Travel between buildings on campus may be necessary. Valid drivers licence and access to vehicle is preferred.

Additional InformationAccommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.caWe thank all applicants within commuting distance of Toronto, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.NO AGENCIES, CALLS OR EMAILS PLEASEQuick Apply

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