Key Responsibilities:

• Lead end-to-end introduction of new materials, including analytical strategy, method transfer/validation, specifications, and QC deliverables
• Support implementation of new technologies in the QC laboratory
• Provide technical expertise for troubleshooting, deviations, investigations, and CAPAs
• Represent QC in cross-functional projects and act as QC point of contact
• Contribute to supplier qualification, audits, and risk assessments
• Ensure GMP compliance of laboratory activities, methods, and documentation
• Act as a subject matter expert, mentor team members, and support daily operations
• Manage and review QC documentation (protocols, reports, procedures)
• Support inspections and ensure adherence to EHS standards

Profile:

• Master’s or PhD in Life Sciences, Chemistry, Pharmacy or equivalent
• ~10 years of experience in a GMP pharmaceutical environment
• Strong expertise in material introduction, analytical methods, and chromatography (HPLC/GC/UPLC)
• Solid knowledge of cGMP, pharmacopeia, validation, data integrity, and QC systems
• Strong problem-solving, communication, and cross-functional collaboration skills
• Fluent in English or French (professional level in the other language)

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

 This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  Employees holding this position will be required to perform any other job-related duties as requested by Management.