Mantell Associates is proud to be partnering with a heavily funded, next-generation biotech company headquartered in Paris in their search for an Interim C-Suite Quality Advisor.
This high-impact, strategic role will support the executive team on an ad-hoc basis, providing expert guidance on GxP quality strategy and governance as the organisation scales.
This is a remote, part-time engagement requiring 8–16 hours per month (typically 1–2 days), with an initial 12-month term and potential progression to a Board-level appointment.
C-Suite Quality Advisor - Responsibilities:
Advise the CEO and executive leadership on overall Quality strategy across GxP functions (GMP, GLP, GCP)
Provide expert input on regulatory inspection readiness, QMS implementation, and global compliance planning
Support the build-out of quality frameworks and operational excellence as the company moves through key development milestones
Represent the quality function at strategic meetings and advise on cross-functional integration
Offer high-level mentorship to internal quality leadership and contribute to board-level discussions where appropriate
C-Suite Quality Advisor - Requirements:
Extensive senior-level experience in Quality Assurance within the biotech, pharmaceutical, or advanced therapy sectors
Proven track record in advising or leading GxP compliance strategies at the C-Suite or Board level
Excellent communication skills and executive presence
Available to commit 1–2 days per month over a 12-month interim period
For more information on this opportunity, contact us at +44 (0)20 3854 7700.