Quality Control Analytical Chemist Ii - Oakville, Canada - Eurofins Canada BioPharma

Eurofins Canada BioPharma

Verified Company

Oakville, Canada

1 week ago

Posted by:

Sophia Lee

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Description

Company Description
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Eurofins 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.
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_ 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._

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Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients "API's") as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its stateoftheart organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths._

Job Description:

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.

Qualifications:

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 problemsolving, planning, and organizational skilled coupled with a strong attention to detail.
Ability to work independently under mínim