Manager, Vendor Relationship in London

Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to unlocking urgently needed new treatment options in mental health care. The Company is headquartered in London, UK, with a U.S. office in New Jersey. We believe mental health patients deserve the possibility of a better future. Our initial focus is developing COMP360 psilocybin, a proprietary, investigational, synthetic psilocybin treatment under evaluation for treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). COMP360 is a potentially first-in-class treatment and has Breakthrough Therapy designation from the U.S. Food and Drug Administration (FDA), as well as Innovative Licensing and Access Pathway (ILAP) designation in the UK for TRD. We are leading the world’s largest classic psychedelic clinical program in TRD, and building upon that robust foundation, we are executing a late-stage trial evaluating COMP360 for PTSD, another condition with high unmet need. Our goal is to advance treatments that move the field of psychiatry towards treatment options that offer rapid onset and sustained durability with infrequent dosing.

The Manager, Vendor Relationship will serve as the main operational point of contact for Compass CDMO/CMOs, and critical material suppliers in our clinical and commercial supply chain. Reporting directly to Supply Chain leadership, this position manages the high-complexity vendor landscape inherent to Scheduled controlled substances.

Location: Remote in the United Kingdom.

Reports to: Associate Director, Supply Chain.

Roles and responsibilities:

• Responsible for the end-to-end management of supply chain vendors to ensure availability of outsourced Drug Substances, Drug products or Finished Goods.
• Identify critical issues and risks, develop action plans, and keep stakeholders apprised of any impact upon supply.
• Collect and maintain relevant information on the entities such as contractual terms, financial expenses and strategic road maps.
• Ensure the accountability for the entities’ performance.
• Set up business review meetings to report on performance, action plan and recommendations.
• Supervise the collection and review of KPIs (Supply Chain, Finance, Quality, etc.).
• Coordinate vendor schedules to secure timely, GXP-compliant manufacturing and distribution of Schedule 1 materials for active global Phase 2/3 clinical protocols.
• Drive the dual-track operational strategy: manage supply chain flexibility for clinical needs while supporting process-scale frameworks with commercial vendors.
• Collaborate with Regulatory Affairs and supply chain to ensure timelines are met for the application and procurement of applicable manufacturing and distribution licenses.
• Vendor management oversight to ensure supply quotas for manufacturing and supply sites are delivered on time and fulfilled.
• Serve as primary relationship owner for CDMOs, CMOs, driving routine external and internal meetings.
• Partner with Supply Chain and legal leaders to negotiate Master Services Agreements (MSAs), Statements of Work (SOWs), and commercial supply agreements with highly structured SLAs.
• Oversee vendor risk assessments and formulate proactive dual-sourcing strategies to mitigate high-barrier entry constraints of scheduled product manufacturing.
• Responsible for the project management of resources to resolve supply issues and support life cycle management in coordination with all stakeholders.
• Review and manage the CMC Manufacturing Financial budget for Clinical and Commercial manufacturing.

Candidate profile:

• Desirable: BSc in a Life Sciences discipline or relevant experience with 2-3 years spent in a similar role.
• Minimum: BSc or equivalent in a Life Sciences or Engineering discipline, with 1-2 years spent in a similar role, e.g. chemistry or biochemical engineering.
• Experience project managing manufacturing/packaging initiatives in the CGMP industry.
• Broad knowledge of biotech/pharmaceutical manufacturing processes with excellent scientific analysis and interpretation skills and the ability to creatively problem solve.
• Controlled Substance Expertise: Experience handling Scheduled controlled drugs, including specialized vault requirements, high-security logistics, and quota management.
• Regulatory Knowledge: Understanding of MHRA, FDA cGMPs, DEA regulations governing high-restriction pharmaceutical components.
• Cross-Functional Fluency: Exceptional ability to translate technical CMC complexities into actionable Vendor management supporting supply chain and technical teams with planning and logistics requirements.
• Strategic Versatility: Competent at switching between the agility needed for clinical trial troubleshooting and the rigid process control needed for commercial launch.

These include flexibility & generous time off, parental & reproductive support, health & medical, mental health & wellbeing and Financial health.

Equal opportunities:

We are committed to building a workplace where everyone’s wellbeing matters. If you need reasonable accommodation during the interview process to be at your best, please let our recruiting team know.

We are proud of our commitment to diversity and equality (pursuant to the Equality Act 2010). We do not discriminate based upon race, religion or belief, colour, nationality, ethnic or national origin, gender, pregnancy or maternity, marital or civil partner status, sexual orientation, gender reassignment, age or disability.

Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying.

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