IN 2024, EUROFINS GENERATED TOTAL REVENUES OF EUR 6.515 BILLION, AND HAS BEEN AMONG THE BEST PERFORMING STOCKS IN EUROPE OVER THE PAST 20 YEARS.

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 state-of-the-art 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

Eurofins CDMO Alphora is looking for a dynamic Quality Control Analytical Chemist to join our Team! The ideal candidate will:

• possess a high degree of initiative
• is a team player with excellent communication abilities
• is comfortable in a modern, state of the art laboratory
• has practical experience with HPLC, GC, KF and various wet chemistry techniques
• has a strong attention to detail and a comprehensive understanding of cGMP
• has strong organizational skills with the ability to multitask and work in a fast-paced environment

Our 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.

Qualifications

QUALIFICATIONS

• Diploma or degree in a related field (Chemistry is preferred), and relevant work experience in analytical laboratory or in a pharmaceutical or other regulated environment is an asset,
• 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.

• 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