GMP Compliance Consultant and 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

Job title: GMP Compliance Consultant and QP

Reporting to: Quality and QP Lead

Department: Consultancy

No of Direct reports: 0

Location: Home based

Summary:

eXmoor Pharma is the only integrated cell and gene therapy CDMO with over 20 years of consultancy expertise embedded across every stage of the CMC journey - from early-phase strategy to process development, GMP manufacturing and commercialisation. We provide comprehensive support across Viral Vectors, Autologous and Allogeneic Cell Therapies, and RNA technologies. This integrated model enables seamless progression from early-phase strategy through to commercial readiness.

We are looking for a Qualified Person (QP) to join our team of QPs eligible to be named on UK or EU Manufacturing Authorisations, with experience with ATMP dosage forms.

This is an exciting opportunity to work with eXmoor’s globally recognised team of scientists, consultants, and engineers, on a wide range of Client projects in a rapidly growing market.

Job Description:

Job Purpose:

You will take part in a range of projects, including acting as a contract QP for eXmoor’s clients manufacturing ATMPs and synthetic gene therapies. Working with the Consultancy team and the Client you will ensure principles of GMP are embedded within the project, whilst supporting the client in achieving their goals.

The role offers the opportunity to work on exciting projects providing expert strategic CMC advice to ATMP developers, representing clients in meetings with medicines regulators, supporting investors with technical expertise and due diligence, influencing the design of new manufacturing facilities, and auditing outsourced manufacturers and suppliers. Furthermore, you will support eXmoor’s CDMO state-of-the-art manufacturing CGT Centre.

Working across a wide portfolio of projects you will ensure delivery of project deliverables to meet customer needs, whilst building and maintaining the client relationship.

You will build and develop an industry network and use that network to support the development of new opportunities and client relationships.

Main areas of responsibility/key duties:

• Taking a lead role in projects interfacing with a clients’ senior management team
• Acting as an internal compliance consultant for the eXmoor pharma business.
• QP certification of ATMP products
• Providing GMP compliance consultancy in all areas of GMP Biomanufacturing and Compliance including:Routine and Legal Duties of a QP on client’s and eXmoor’s manufacturing sites
• Client User Requirement Briefs and Specifications
• Process & Analytical Development, qualification and validation
• Pharmaceutical Quality System development and management
• Planning & preparation for manufacturing
• Facility Operations and Qualification
• Preparation for Facility Manufacturing Authorisation applications
• Manufacturer and Supplier Auditing
• CMC Regulatory consultancy
• Product licensing (Clinical Trial and Marketing Authorisation applications)
• Production and materials controls
• QC strategy and analytical method validation
• Final product release

Person Specification:

Essential Qualifications & Experience:

• BSc in a relevant biotechnology area
• Technical experience (5 years plus) with ATMPs in at least one of the following areas:
• Process/Analytical Development, GMP Manufacturing & QC, Capital Projects
• Operations Management in a senior position undertaking one or more of the following:
• Bioprocess development, Analytical development, Technology transfer, GMP biomanufacturing, GMP Quality Control
• Extensive Compliance and Regulatory experience within the UK & EU Regulatory Framework for manufacture of ATIMPS and ATMPs (MHRA, EMA, HTA) with a role undertaking one or more of the following:
• GMP Pharmaceutical Quality System Development and Management, Auditing, Facility licensing and QP product certification, Clinical trials and product licensingEligibility to act as EU/UK Qualified Person

Desirable Qualifications & Experience:

• Extensive technical experience (10 years plus) with ATMPs in GMP Manufacturing & QC
• Technical experience with manufacturing synthetic gene therapy or nucleic acid vaccine
• Experience within a Capital Projects role undertaking one or more of the following:
• Project Management, URB and GMP compliance, Facility Qualification to PQ and handover to operations
• Experience with writing sections of Clinical Trial Applications for ATMPs, Marketing Authorisations, and preparation for and attendance at regulatory interaction meetings for e.g.:
• US FDA IND or BLA filings, EU EMA CTA or MAA filings, UK MHRA CTA or MAA filing
• MSc/PhD in a relevant biotechnology area.
• An Industry network of potential clients.
• Experienced consultant or has operated in a client facing role.
• Regulatory Experience within other national competent authorities, e.g. China, Japan, Australia.

Competences Required:

• Technical Competencies in either or both of common ATMP production or analytical development & manufacturing.
• Pharmaceutical Quality System Development & Management.
• Regulatory Inspections & facility licensing
• Facility Qualifications
• Auditing
• Developing a business case
• Developing business & project strategy
• Market knowledge in manufacturing of ATMPs
• Ability to influence and persuade
• Self-starter with "can do" attitude who gets things done
• Planning, organising, logical
• Innovation, open to new ideas
• Excellent written and verbal communications
• Team member and team leader
• Expert user of MS Office
• Familiar with collaborative working tools