Freelance GCP Auditor (Canada-based)

ProPharma; Windsor; On-site; CAD 80,000 - 120,000; Full time

Job summary

ProPharma seeks a Freelance GCP Auditor based in Canada to lead QA projects, conduct GCP audits, and develop Quality Management Systems. The ideal candidate has over 10 years of clinical compliance experience, including leadership roles, and excels in communication and analytical skills.

Qualifications

• 10+ years of clinical compliance and GCP auditing experience.
• At least 5 years in leadership roles.
• Proven success in managing high-performance teams.

Responsibilities

• Lead Quality Assurance Projects and conduct GCP audits.
• Develop and oversee Quality Management Systems (QMS).
• Draft and refine Standard Operating Procedures (SOPs).

Skills

GCP compliance

Audit experience

SOP writing

Regulatory response development

Analytical skills

Communication skills

Job description

Join to apply for the Freelance GCP Auditor (Canada-based) role at ProPharma

ProPharma has been dedicated to improving patient health and wellness for over 20 years by providing expert advice and solutions to biotech, med device, and pharmaceutical organizations. We partner through an advise-build-operate model across the entire product lifecycle, leveraging deep expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology. Our fully customizable consulting services help de-risk and accelerate high-profile drug and device programs.

Position : Freelance GCP Auditor (Canada-based)

Note : Not open to third-party agencies.

What You’ll Do

• Lead Quality Assurance Projects : Conduct GCP audits, including specialized areas such as biologics, vaccines, and Cell / Gene therapies.
• Develop and oversee Quality Management Systems (QMS).

Drive Technical Excellence

• Draft and refine Standard Operating Procedures (SOPs).
• Provide tailored GxP compliance consulting based on client needs.
• Stay updated on regulatory and technological changes to deliver innovative solutions.

What We’re Looking For

Experience & Expertise

• 10+ years of clinical compliance and GCP auditing experience, including at least 5 years in leadership roles.
• Proven success in managing high-performance teams and complex projects.

Technical Skills

• Deep understanding of GCP compliance requirements.
• Experience performing audits.
• Proficiency in SOP writing and regulatory response development.

Desired Qualities

• Excellent communication and persuasion skills.
• Strong analytical skills and attention to detail.
• Commitment to diversity, equity, and inclusion.

We celebrate diversity and strive to create an inclusive workplace where everyone can be their authentic selves. ProPharma is an Equal Opportunity Employer committed to fostering a safe and empowering environment for all employees.

Note : ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please do not contact us by phone or email regarding this posting.