Quality Control Analytical Chemist I - Eurofins CDMO Alphora

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 fastpaced 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 :

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) and relevant work experience in analytical laboratory or in a pharmaceutical or other regulated environment is an asset
• Excellent documentation and communication skills.
• Excellent problemsolving planning and organizational skilled coupled with a strong attention to detail.
• Ability to work independently under minimal supervision.

Additional Information :

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

At Eurofins we offer excellent fulltime benefits including health & dental coverage life and disability insurance RRSP with 3% company match paid holidays paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process or those needing job postings in an alternative format may email 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.

NO AGENCIES CALLS OR EMAILS PLEASE

Remote Work :

No

Employment Type :

Fulltime