MedTech Quality Systems & Compliance Specialist (Contract)

Johnson & Johnson; Markham; On-site; CAD 65,000 - 104,000; Full time

Benefits offered by this job

Flexible benefits

Medical, dental, vision coverage

3 weeks vacation + 4 floater days

5 personal time-off days

5 Sick days

2 volunteer days per year

RRSP company match

Job summary

Johnson & Johnson is seeking a Quality Systems & Compliance Specialist for an 18‑month contract in Markham, ON. You will maintain the Quality Management System, support regulatory inspections, and ensure compliance across the distribution network.

The role requires 2–4 years in a regulated environment with strong knowledge of GMP/GDP and Canadian regulations. You will collaborate with Cross-functional teams and manage supplier quality activities.

Qualifications

• Minimum 2–4 years of experience in a regulated environment (device/pharma).
• Strong knowledge of medical device and/or pharma Quality Management Systems.
• Experience with regulatory inspections and internal/external audits.
• Experience with distribution practices for regulated products and change controls.
• Ability to work in a matrix environment with multiple stakeholders and priorities.

Responsibilities

• Oversees and supports Markham SDC’s daily issues or inquiries.
• Supports strategies and metrics to deliver compliance and credo goals.
• Integrates quality systems into critical business areas (receipts, storage, supplier management, NCRs).
• Supports regulatory inspections and audits; leads corrective actions.
• Acts as Master Data Governance functional steward for MT Surgery Commercial Quality.

Skills

Quality Systems

Regulatory Compliance

GMP

GDP

Quality Management

Education

BSc Life Sciences

Quality Certification (PG)

Job description

Johnson & Johnson is seeking a Quality Systems & Compliance Specialist for an 18‑month contract in Markham, ON. You will maintain the Quality Management System, support regulatory inspections, and ensure compliance across the distribution network.

The role requires 2–4 years in a regulated environment with strong knowledge of GMP/GDP and Canadian regulations. You will collaborate with Cross-functional teams and manage supplier quality activities.