Join Catalent as a Quality Assurance Associate in Adair, ON and play a key role in pharmaceutical product compliance. Contribute to manufacturing excellence through audits and staff training.
This position emphasizes maintaining high quality and compliance standards in pharmaceutical production. You will perform critical audits and assist in coaching employees on best practices while supporting the facility's innovative startup phase.
Key Responsibilities:
- Conduct in-process audits and relay findings to production
- Ensure compliance through final release document audits
- Investigate deviations and coach staff on improvement
- Execute compliance audits and generate management reports
- Act as QA representative to resolve manufacturing issues
Requirements:
- Bachelor's Degree in a relevant scientific field
- Excellent manual dexterity and attention to detail
- Strong analytical and communication skills
- Able to work self-sufficiently with little oversight
- Experience in a pharmaceutical or GMP environment is a plus
Help elevate product quality and contribute to patient outcomes at Catalent's state-of-the-art facility.
Catalent Quality Assurance Associate Role employer: Catalent Pharma Solutions
Catalent is an exceptional employer that prioritizes employee growth and development within a collaborative and innovative work culture. Located in Adair, Ontario, our facility offers a supportive environment where you can thrive while contributing to the production of life-changing pharmaceutical products. With a focus on continuous improvement and adherence to GMP standards, we provide meaningful opportunities for career advancement and a commitment to employee well-being.
