Jobs in Mississauga, Canada

About the role

The QA Associate – Biologics is accountable to the QA Manager, Biologics and plays a key role in supporting Eurofins CDMO Alphora Inc.’s compliance with Current Good Manufacturing Practices (cGMP) to ensure the production of safe and efficacious clinical and commercial pharmaceuticals on behalf of our clients and their patients. The QA Associate – Biologics supports quality oversight of GMP activities within the Biologics operating unit, including the development and commercialization of biotechnology-derived pharmaceuticals such as monoclonal antibodies (mAbs), mammalian-based therapeutic proteins, and antibody-drug conjugate (ADC) candidates. Biologics GMP operations include a clinical GMP cleanroom suite, GMP analytical/QC laboratory, and large-scale GMP manufacturing facility with sterile fill-finish capabilities. The starting annual base compensation for this position is $70,000 CAD. The actual offer, reflecting the total compensation package plus benefits, will be determined by a number of factors which include but are not limited to the applicant’s experience, knowledge, skills, and abilities. 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.ca

What you'll bring

• 2-5 years of pharmaceutical quality experience
• Experience with development, manufacture, packaging and testing of pharmaceuticals
• Strong understanding of cGMP and related Regulations
• Strong written and verbal skills are a priority
• A proficiency for multi-tasking
• Excellent interpersonal skills
• Good time management and project management skills
• A focus on attention to detail
• Be goal orientated and results driven
• A desire to learn and for continuous development
• Experience with Biologic pharmaceutical, in particular mAbs and ADCs is an asset
• Sterile fill / aseptic processing experience preferred.

Benefits