At a Glance
- Tasks: Lead quality assurance projects and ensure compliance in the pharmaceutical industry.
- Company: Join a reputable consulting firm focused on quality and compliance.
- Benefits: Competitive pay, flexible hours, and valuable industry experience.
- Other info: Opportunity to work with top professionals and enhance your career.
- Why this job: Make a difference in healthcare by ensuring product safety and compliance.
- Qualifications: Experience in GMP and strong regulatory knowledge required.
The predicted salary is between 76500 - 93500 $ per year.
Q C is seeking a Quality Assurance professional for a six-month pharmaceutical GMP consulting engagement in Mississauga.
You will work within a team to apply in-depth regulatory knowledge and deliver compliant, timely solutions for deviations, change controls and audits.
Reporting to the VP Consulting Services, you will plan, organize and manage projects, review batch documentation, support product release, and host Health Canada audits while coordinating with client personnel to meet goals.
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Contract GMP QA Lead in Mississauga employer: Q C
At Q C, we pride ourselves on fostering a collaborative and innovative work environment that empowers our employees to excel in their roles. As a Contract GMP QA Lead in Mississauga, you will benefit from our commitment to professional development, competitive compensation, and a supportive culture that values compliance and quality. Join us to make a meaningful impact in the pharmaceutical industry while enjoying the unique advantages of working in a vibrant city known for its diverse community and opportunities.
