Lead country quality and compliance activities for products sold in CanadaMaintain the local QMS and author or approve BDF Canada SOPs, quality reports and controlled recordsOversee Canadian product release, stability and microbiological testing, deviations, OOS investigations and CAPAMaintain Drug Establishment, medical-device and site licenses and support DIN/NHP registrations and launchesApprove DIN, NHP, cosmetic and medical-device labels;

review claims and advertising materials when requiredLead cross-functional quality activities through coaching, collaboration and technical expertise.Support product availability and coordinate with Planning, Purchasing, Customer Service, Finance, Sales, Packaging and MarketingServe as the point person for Canadian quality issues and advise the business on compliance mattersAssess, communicate, escalation and mitigate quality risks that may impact product quality, consumer safety, regulatory compliance or business continuity while maintaining alignment with cross-functional partners.Manage qualification and quality oversight of warehouses, QC consultants, external laboratories, PCs, 3PMs, distribution centres, carriers and VAS providersEstablish and maintain quality agreements with BDF Canada contractors and service providersAudit external partners such as Accuristix, Harling and RD Labs and BDF manufacturing sites including BMP and BMMOversee VAS batch release and documentation, finished-goods release records and complaint investigationsDevelop suppliers through re-audits and troubleshooting;

initiate and verify effective CAPAReduce consulting costs by conducting external site audits directly where appropriateYour Tasks

Lead country quality and compliance activities for products sold in CanadaMaintain the local QMS and author or approve BDF Canada SOPs, quality reports and controlled recordsOversee Canadian product release, stability and microbiological testing, deviations, OOS investigations and CAPAMaintain Drug Establishment, medical-device and site licenses and support DIN/NHP registrations and launchesApprove DIN, NHP, cosmetic and medical-device labels;

review claims and advertising materials when requiredLead cross-functional quality activities through coaching, collaboration and technical expertise.Support product availability and coordinate with Planning, Purchasing, Customer Service, Finance, Sales, Packaging and MarketingServe as the point person for Canadian quality issues and advise the business on compliance mattersAssess, communicate,



escalation and mitigate quality risks that may impact product quality, consumer safety, regulatory compliance or business continuity while maintaining alignment with cross-functional partners.Supplier Management:

Manage qualification and quality oversight of warehouses, QC consultants, external laboratories, PCs, 3PMs, distribution centres, carriers and VAS providersEstablish and maintain quality agreements with BDF Canada contractors and service providersAudit external partners such as Accuristix, Harling and RD Labs and BDF manufacturing sites including BMP and BMMOversee VAS batch release and documentation, finished-goods release records and complaint investigationsDevelop suppliers through re-audits and troubleshooting;

initiate and verify effective CAPAReduce consulting costs by conducting external site audits directly where appropriateProduct Compliance:

Manage medical-device lifecycle compliance and complaintsConduct internal PC audits and support Hamburg with DEKRA medical-device auditsMaintain MSDS information and ensure regulatory documentation remains currentCollaborate with R&D; and Hamburg on claims support, compliance and product-launch requirementsQuality Management:

Own and maintain the effectiveness of the Canadian Quality Management System through KPI monitoring, management review, quality planning, escalation management and continuous improvement activities.Lead complaint trending, root-cause investigation, CAPA and PPM-reduction initiativesDrive risk-based decision making through trend analysis, complaint monitoring, CAPA effectiveness reviews and management-review activities.Conduct internal GMP training and support audit readinessExecute and evaluate on-shelf store checks;

drive corrective actions and complete monthly reportingManage MCS and Cal Labs Quality budgets for stability testing, microbiological testing and product releaseEnsure local processes align with North America, Global Quality and applicable Canadian requirementsMaintain continuous readiness for Health Canada, corporate, customer and third-party inspections through effective Quality System oversight,



internal audit programs and timely resolution of identified gapsEnsure Quality Management System processes remain compliant, effective and aligned with North America, Global Quality and applicable Canadian regulatory requirements.Manage interdepartmental relationships, deliverables, and stakeholders to achieve compliance and continuous improvement.Your Profile

7+ years of related Quality or Regulatory Affairs experience in a regulated consumer-products environmentStrong knowledge of Canadian DIN, NHP, cosmetic and medical-device requirementsStrong knowledge of GMP, QMS, audits, complaints/ADRs, investigations, CAPA, change control and product releaseUniversity degree in a relevant technical discipline;

Biology, Engineering, Microbiology, Chemistry or related field preferredStrong analytical, problem-solving, decision-making and communication skillsStrong project-management capability with strategic thinking and tactical focusDetail-oriented team player who organizes multiple priorities with reliable follow-throughStrong oral and written communication;

presents technical and regulatory information clearlyAbility to lead, facilitate and influence cross-functional decisionsContinuous-improvement mindset;

resilient in dynamic situations;

English required, French an assetAdditional Information

At Beiersdorf, we value diversity and aim to provide equal opportunities to all of our applicants – regardless of e.G. gender, sexual identity, nationality, ethnicity, religion or ideology, disability or age. We would therefore ask you to include only information and data in your documents which are relevant for the assessment of your application (e.G. curriculum vitae with relevant references and certificates). For instance, please feel free to upload your CV without a picture.Beiersdorf North America - Recent Awards

Winner of Comparably's Award for Best Company Outlook (2021, 2024, 2025)Winner of Comparably's Award for Best Company Work Life Balance (2025)Winner of Comparably's Award for Best Company Culture (2023, 2024)Winner of Comparably's Award for Best Company Compensation (2020, 2022-2024)Winner of Comparably's Award for Best Company Perks and Benefits (2024, 2025)Winner of Comparably's Award for Best Company for Happiness (2022,2023, 2024, 2025)Winner of Comparably's Award for Best CEO / General Manager (2020, 2024)Winner of Comparably's Award for Best Sales Team (2023, 2024, 2025)Winner of Comparably's Award for Best Leadership Teams (2020, 2021, 2023, 2025)Winner of Comparably's Award for Best Company for Diversity (2022)Beiersdorf is an Equal Prospect Employer.

📌 Senior Quality Manager (Winnipeg)
🏢 BEIERSDORF
📍 Winnipeg