Remote GMP Compliance Consultant & QP

eXmoor Pharma; United States; Remote; GBP 85,000 - 110,000; Full time

Job summary

eXmoor Pharma is seeking a Qualified Person (QP) with GMP compliance expertise to lead QA and regulatory activities for ATMPs and gene therapies. You will act as contract QP for clients and ensure GMP principles are embedded across projects within a Consultancy team.

You will collaborate with regulators, investors, and manufacturing partners, supporting facility readiness, licensing, and due diligence while expanding eXmoor’s CDMO capabilities in CGT. Home-based in the UK.

Qualifications

• 5+ years of experience in ATMP GMP environments.
• Experience with UK/EU regulatory frameworks (MHRA/EMA).
• Proven ability to certify ATMP products as Qualified Person (QP).
• Strong understanding of GMP Biomanufacturing and QC roles.
• Experience leading multi-disciplinary projects and client-facing roles.

Responsibilities

• Lead projects interfacing with a client’s senior management team.
• Act as internal compliance consultant for the business.
• Provide QP certification for ATMP products.
• Deliver GMP consultancy across biomanufacturing and compliance domains.
• Prepare and review regulatory submissions and licensing materials.
• Audit manufacturers and suppliers and manage quality systems.

Skills

ATMP knowledge

GMP compliance

Regulatory inspections

Stakeholder management

Quality systems

Education

BSc in biotechnology

MSc/PhD in biotechnology

Tools

MS Office

Job description

eXmoor Pharma is seeking a Qualified Person (QP) with GMP compliance expertise to lead QA and regulatory activities for ATMPs and gene therapies. You will act as contract QP for clients and ensure GMP principles are embedded across projects within a Consultancy team.

You will collaborate with regulators, investors, and manufacturing partners, supporting facility readiness, licensing, and due diligence while expanding eXmoor’s CDMO capabilities in CGT. Home-based in the UK.