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The Procedure Coordinator is responsible for monitoring, revising, and preparing Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) forms. Key duties include ensuring compliance with regulations, maintaining training records, assisting with training material preparation, and collaborating with the Compliance Department to keep documentation up to date.

The Quality Specialist III will ensure adherence to Standard Operating Procedures for the Annual Product Review (APR) and support the compilation and review of product data. Responsibilities include administrative data entry, report generation, and providing training and support to APR coordinators and associates, while assessing changes to regulatory standards.

The Sr. Manager, Quality and Compliance at Thermo Fisher Scientific will lead the Compliance Program, ensuring adherence to Health Canada, FDA, and EMA GMP requirements while enhancing the Quality Culture. Responsibilities include managing teams for quality metrics, overseeing audits and vendor management, resolving critical issues, and ensuring the facility is inspection-ready. This role also involves mentoring staff and managing departmental budgets and risk initiatives.