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About the role
Key responsibilities & impact- Lead and coordinate quality and regulatory activities from early phases (e.g., candidate selection) through product approval (end-to-end), in alignment with the global R&D strategy, to support Product Science & Technology teams.
- Define, implement, and oversee quality activities for the development of new products and the lifecycle management of Galderma’s current product portfolio.
- Engage with global stakeholders and influence external partners as needed.
- Ensure activities align with global strategies and plans, and comply with applicable regulatory requirements, the quality system, and international standards.
- Provide end-to-end oversight of products manufactured by Galderma entities or outsourced partners.
- Drive proactive risk management and, where applicable, apply Quality by Design principles in collaboration with the Product Technical Lead and development teams.
- Provide quality oversight during process transfers, analytical method transfers, and scale-up to industrial production.
- Liaise and coordinate with the Quality Assurance organization (e.g., Development QA, Manufacturing QA, ESO…), particularly during project transfers to advanced development phases.
- Lead and determine the development and implementation of guidelines, work procedures, and documentation required to fulfill assigned responsibilities.
- Ensure product development quality through clinical batches, development reports, and document review as needed.
- Review and approve (where applicable) regulatory documents (CMC sections for pharmaceutical products / PIF for cosmetic products) and associated documentation (IND, CTA, IMPD, BLA, technical files…)
- Support inspection readiness for launches / PAI and oversee critical/major quality deviations identified during audits, inspections, or complaints, including their investigations.
- Support the Global Head of Quality Development & Lifecycle and collaborate with cross-functional teams to ensure robust business continuity plans are in place to prevent supply interruptions.
Requirements
What you’ll need- PhD in Pharmacy / Engineering degree or Master’s degree in pharmaceutical sciences, cosmetics, chemistry, biology, or a related field;
- Over 8 years of proven experience in Quality within the pharmaceutical or cosmetic industry, including at least 5 years in activities related to the production/development of semi-solids at a global scale;
- Quality management certification (e.g., ASQ Certified Quality Auditor) is an asset;
- Six Sigma / Lean Manufacturing certification is desirable;
- Experience managing remote teams is a plus;
- Strongly recommended experience in global product lifecycle management and oversight of external partners;
- In-depth knowledge of cGMP, GDP, ISO, ICH, and other regulatory requirements relevant to sterile products;
- Excellent communication and interpersonal skills;
- Analytical mindset and strong problem-solving abilities;
- Good leadership and ability to manage multiple projects and priorities simultaneously;
- Ability to operate in a complex, global environment;
- Ability to influence technical and regulatory strategies at global governance level.
Benefits
Comp & perks- Comprehensive group insurance coverage from day one (medical, dental, disability, travel, etc.)
- Employer-paid premium up to 85%
- One of the best retirement plans in Canada (employer contribution up to 10%)
- Profit-sharing program up to 6% of salary
- Excellent work environment with an inspiring atmosphere
- Multiple advancement opportunities
- A work environment where safety is a top priority
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
quality managementproduct lifecycle managementrisk managementQuality by Designregulatory document reviewanalytical method transfersprocess transfersclinical batch oversightdocumentation reviewproject management
Soft Skills
communication skillsinterpersonal skillsanalytical mindsetproblem-solving abilitiesleadershipproject prioritizationinfluencing skillscollaborationteam managementadaptability
Certifications
PhD in PharmacyMaster’s degree in pharmaceutical sciencesASQ Certified Quality AuditorSix Sigma certificationLean Manufacturing certification
