Maxeor Recruitement Inc. Whitby, Ontario
04 juil., 2019Permanent - Temps plein
The firm is a science company. Assists in the development and motivation of above mentioned departments. Provides leadership for Health Products and Food Branch Inspectorate (HPFBI) and Food & Drug Administration (FDA) as well as other regulatory body audits and awareness programs for each agency. Leads audit response teams for both regulatory and client audits. Assists in the development of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) policies for all departments. Ensures departments conform to GMP and GLP policies. Bachelor of Science (B.Sc.) in Chemistry, Pharmacy, Microbiology, or Biology. Minimum 10 years of Quality Assurance experience within the pharmaceutical industry with a minimum of 5 years experience managing direct reports. Minimum 5 years of FDA/HPB exposure as a Senior Quality Manager within the pharmaceutical industry. Extensive FDA audit/audit response background. Possesses a highly developed quality, regulatory and production mindset including an appreciation for client service and contract manufacturing. Exceptional Good Manufacturing Practices knowledge.