Sr. Manager, CQ Lead Canada

DePuy Synthes is recruiting for a(n) Sr. Manager CQ Lead Canada in Commercial Qualitylocatedin Toronto Ontario Canada.

Job Overview

The Sr. Manager CQ Lead Canadais responsible forleading Commercial Quality activities for the Canada local market. This role ensures that commercial distribution and postmarket activitiescomply withapplicable regulatory requirements quality system standards and internal policies. The position has a significant impact on patient safety regulatory readiness and business performance by serving as the senior Commercial Quality leader for Canada and partnering closely with Commercial Regulatory Affairs Supply Chain and Global Quality teams.

Key Responsibilities

• Lead and oversee Commercial Quality activities for the Canada market in alignment with global quality and compliance strategies.

• Ensure adherence to Canadian regulatory requirements internal policies and quality system standards across commercial operations.

• Serve as the primary Commercial Quality point of contact and escalation lead for the Canada local operating company.

• Partner with Commercial Regulatory Affairs Quality and Supply Chain teams to support compliant product distribution and lifecycle activities.

• Support postmarket surveillance activities including complaint handling vigilance and field action coordination.

• Lead audit andinspectionreadiness including internal audits external audits and health authority inspections.

• Monitor quality trends risks and performance metrics and drive corrective and preventive actions.

• Lead coach and develop Commercial Quality team members fostering a strong quality culture.

Qualifications

Education:

• Bachelors degree in Quality Engineering Life Sciences Regulatory Affairs ora relateddiscipline (required).

• Advanced degree in a scientific quality or regulatory field (preferred).

Experience and Skills:

:

• Typically810 years of progressive experience in Quality Regulatory or Compliance roles within a regulated industry.

• Strong working knowledge of qualitysystemand regulatory requirementsimpactingcommercial operations.

• Experience supporting audits inspections and health authority interactions.

• Demonstrated ability to lead local quality execution and influence crossfunctional stakeholders.

Preferred:

• Experience in medical devices healthcare or other highly regulated industries.

• Familiarity with Canadian regulatory requirements and Health Canada expectations.

• Experience working in a global or matrixed organization.

• Exposure to postmarket surveillance anddistributionquality activities.

• Quality or Regulatory certifications (e.g. RAC ASQ).

• Strong analytical organizational and problemsolving skills.

• Effective written and verbal communication skills.

Other:

• Language: English; French preferred.

• Travel: Limited; occasional domestic or regional travel.

• Certifications: Quality or Regulatory certifications preferred but notrequired.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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