Quality Control Analytical Chemist II - Eurofins CDMO Alphora

You 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.

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 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 Information :

Accommodation: 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 .

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 

We thank all applicants within commuting distance of GTA Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

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Remote Work :

No

Employment Type :

Full-time