Join Catalent in Windsor, Ontario as a Quality Assurance Associate dedicated to quality excellence and compliance. This onsite role emphasizes proactive prevention of quality issues through effective training and documentation practices.
In this critical role, you will foster a culture that prioritizes compliance and continuous improvement within the manufacturing process. Engage in in-process batch reviews and provide coaching to operators regarding cGMP compliance. By initiating and managing manufacturing deviations, you will help ensure that products meet the highest standards of quality before release.
Key Responsibilities:
• Execute in-process reviews of quality documentation • Facilitate training on cGMP and documentation practices • Conduct line clearance verifications during changeovers • Serve as Quality Assurance point of contact on shift • Maintain logs for operational areas and compliance
Requirements: • Bachelor’s degree in science, Chemistry or Biochemistry preferred • Background in GMP or pharmaceutical manufacturing • Excellent communication and interpersonal skills • Detail-oriented with the ability to work independently • Verification of foreign credentials required
Contribute to Catalent’s mission to enhance patient outcomes through superior quality assurance. #J-18808-Ljbffr