GXP Auditor (Freelance)

TL;DR

GXP Auditor (Freelance): Conducting quality and compliance audits for biotech, medical device, and pharmaceutical organizations with an accent on regulatory standards and product lifecycle integrity. Focus on ensuring adherence to GXP requirements and supporting the advancement of scientific breakthroughs through rigorous quality oversight.

Location: Must be based in the United Kingdom. Hybrid work is encouraged for those within commuting distance of an office.

Company

hirify.global provides expert consulting and operational support to biotech, med device, and pharmaceutical organizations across the complete product lifecycle.

What you will do

• Perform GXP audits to ensure compliance with regulatory standards.
• Evaluate quality systems and processes within pharmaceutical and biotech environments.
• Provide expert advice to clients on regulatory sciences and quality compliance.
• Collaborate with cross-functional teams to de-risk and accelerate drug and device programs.
• Document audit findings and recommend corrective actions.

Requirements

• Must be based in the United Kingdom.
• Proven experience in GXP auditing within the pharmaceutical or medical device industry.
• Strong understanding of regulatory compliance and quality management systems.
• Ability to work independently as a freelance professional.
• Excellent communication skills for reporting and stakeholder management.

Culture & Benefits

• Commitment to diversity, equity, and inclusion in the workplace.
• Supportive environment that values innovative and entrepreneurial spirits.
• Flexible working arrangements with support for remote and hybrid models.
• Opportunity to work on high-profile drug and device programs.