Quality Assurance Specialist: Senior Position in Pharmaceuticals, Lévis

Become a key player as a Senior Quality Assurance Specialist dedicated to pharmaceutical products. This full-time role emphasizes specification development and compliance in a dynamic environment.

You will manage specifications for raw goods, packaging, and finished items, ensuring rigorous quality assurance processes. Reporting to the quality lead, you'll address change control issues, help investigate quality events, and enhance industry protocols. Your leadership will be pivotal in shaping quality standards that safeguard health.

Key Responsibilities:• Create comprehensive specifications for pharmaceutical products • Write risk assessments related to product quality • Oversee change controls associated with specifications • Participate in quality investigations and customer complaints • Revise analytical methods from the lab as needed

Requirements:• Bachelor's degree in science; chemistry or biochemistry preferred • At least 5 years in pharmaceutical industry roles • Strong understanding of cGMP regulations in both Canada and the U.S. • Excellent organizational and communication skills • Proven ability to manage projects and lead teams

Position yourself at the forefront of pharmaceutical quality assurance, where your expertise makes a lasting impact on health and wellness. #J-18808-Ljbffr