
Compass Pathways · London
Company introduction: Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in m...
Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based
innovation in mental health. The Company is headquartered in London, UK, with offices in New York City in the US. We focus on
developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions
and who are not helped by current treatments.
We are pioneering a new paradigm for treating mental health conditions focused on rapid and durable responses through the
development of our investigational COMP360 synthetic psilocybin treatment, potentially a first in class treatment. COMP360 has
Breakthrough Therapy designation from the US Food and Drug Administration (FDA) and has received Innovative Licensing and Access
Pathway (ILAP) designation in the UK for treatment-resistant depression (TRD) due to the pressing unmet need in this area.
We are currently in phase 3 for TRD, have completed phase 2 studies for both post-traumatic stress disorder (PTSD) and anorexia
nervosa and are planning a further late-stage study in PTSD. We envision a world where mental health means not just the absence of
illness but the ability to thrive. - Compass Pathways.
The Team Coordinator, R&D is a pivotal support role at the heart of Compass' scientific engine. As a key partner to our research
and development teams, you will provide the essential administrative and executive support that enables our Research & Development
Leadership Team (RDLT) to pioneer the future of mental health treatment.
Location: Hybrid in our London office (2x/week in-office).
Reports to: VP, Manufacturing & Supply. This position will support various leadership roles within the R&D function.
Roles and responsibilities
System, ensuring participant safety, data integrity, and accuracy throughout the trial process
Outlook, Word, PowerPoint, OneDrive), Adobe (including advanced PDF handling), and DocuSign
For an overview of our benefits package and compensation information, please visit "Working at Compass".
Reasonable accommodation
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.
UK applicants
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.
US applicants
Compass Pathways is proud to be an equal opportunity employer. All employment decisions are based on business needs, job
requirements, and individual qualifications, without regard to race, religion, color, national origin, sex (including pregnancy,
childbirth, and related medical conditions), ethnicity, age, disability, sexual orientation, gender identity, gender expression,
military service, genetic information, familial or marital status, or any other status, category, or characteristic protected by
applicable law.
Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to
which you are applying.
All data is confidential and protected by all legal and data privacy requirements, please see our recruitment Privacy Notice to
learn more about how we process personal data.
YOUR MISSION The main purpose of the Advanced Bioprocessing Scientist is to perform advanced manufacturing and continuous improvement activities for the production of sterile gene therapy products in line with current Good Manufacturing Practice (cGMP). JOB DESCRIPTION MAJOR ACTIVITIES * Responsible for driving own development and coaching/training of Bioprocessing Scientists in line with the Training Plan. * Responsible for performing manufacturing activities in multiple unit operations, following all GMP instructions and good practices to manufacture the required products. * Responsible for identifying, reporting and investigating issues and coaching others on investigations. * Responsible for identifying, reporting and where appropriate investigating safety risks and near misses. * Responsible for identifying, collaborating and delivering continuous improvements within the manufacturing area to improve safety, quality and flow. * Responsible for operate appropriately within clean room environment to achieve required level of low bioburden / aseptic operations. * Responsible for routine monitoring of the manufacturing facility to ensure that the facility operates in a compliant and safe manner. * Responsible for performing sanitisation of the manufacturing materials and facility. * Responsible for ensuring materials used within manufacturing are correct, clean, appropriate and in place ready for manufacture to the agreed schedule. KEY PERFORMANCE INDICATORS * Safe working of self and with others. * Compliance with GMP requirements including Data Integrity. * Excellent cleanroom behavour. * Timely closure of GMP commitments (issues, BMRs, CAPA, change control). * Adherence to manufacturing schedule. KEY JOB COMPETENCIES * Aseptic processing - Operates to appropriate manufacturing practices to avoid cross contamination and sterile processing. * Problem Solving - Identifies and resolves problems in a timely manner; able to gather and analyze information; develops alternative solutions; works well in group problem solving situations. * Motivation - sets and achieves challenging goals; demonstrates persistence and overcomes obstacles; measures self against standard of excellence; * Planning/Organizing - prioritizes and plans work activities; uses time efficiently; plans for additional resources; sets goals and objectives. * Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments. * Quality Management - looks for ways to improve and promote quality; demonstrates accuracy and thoroughness. * Oral Communication - speaks clearly; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings. * Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information. * Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures. * Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken. * Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions is closed timely and in a RFT state. JOB RESPONSIBILITIES * Responsible for GxP compliance within designated processing areas. * Accountable for safety of self and team within designated processing areas. JOB BACKGROUND * University degree in Science or Engineering. * Experience in pharmaceutical product manufacture (preference for biologics and aseptic manufacture). * Good awareness of GMP. * Demonstrated competency within multiple areas of MeiraGTx bioprocessing and strong performance in managing quality events.
WHO WE ARE Proxima Fusion is Europe’s fastest-growing fusion company and the continent’s best-funded fusion player, as well as the first spin-out from the Max Planck Institute for Plasma Physics (IPP). Backed by over €650M and powered by a growing team across Munich, Zurich, and Oxford, we are developing the hardware and infrastructure needed to deliver the world’s first commercial stellarator fusion power plant. Our concept advances the most mature fusion technology out there, the Wendelstein 7-X stellarator, through two next-generation machines: Alpha and Stellaris. Our work combines stellarator optimization, advanced computation, machine learning, and high-temperature superconducting magnets to unlock higher-performance designs that were previously out of reach. Turning these designs into a functioning fusion power plant requires excellence and ownership across every discipline, from physics and engineering to software, manufacturing, law, and business functions. WHY JOIN US * Work on a civilisation-scale problem - Clean, baseload fusion energy is one of the few genuinely world-changing challenges, and every hire in Finance, People, or Legal directly accelerates the path to a working stellarator. * Grow as fast as the company does - With headcount set to roughly 5x in a few years and major technical milestones ahead on the path to our demo machine and first power plant, your role grows under you; today's hire is tomorrow's function lead. * Tackle problems that don't exist elsewhere - Fusion sits at a rare intersection of deep-tech R&D, industrial procurement, government relations, and venture financing, so non-tech functions face challenges no other workplace can offer. YOUR IMPACT As a People Operations Specialist, you'll help build the operational foundation that enables our teams to thrive as we grow internationally. Your work will ensure our people processes are efficient, scalable, and employee-centric. WHAT YOU WILL DO * Coordinate day-to-day people operations so everything runs smoothly across regions. * Manage the administration of key employee lifecycle processes (onboarding, offboarding, etc.) and keep improving how they work. * Spot inefficiencies and suggest practical improvements that align with business priorities. * Use tools and systems to simplify people processes and make them more scalable. * Work closely with teams across the business to drive projects from start to finish. * Maintain clear SOPs and policies so people processes are consistent across locations. * Resolve day-to-day people queries around people topics * Partner effectively with external providers (payroll, benefits, etc.) to ensure smooth and reliable service delivery. * Track compliance and manage risks across the regions you support. WHO YOU ARE * Leading with empathy and sensitivity * Advanced knowledge of HRIS systems, particularly HiBob * Ability to handle complex projects, strong analytical skills, and attention to detail * Familiarity with AI-driven workflows and continuous improvement methodologies * Ability to handle sensitive and confidential information in a professional manner INTERVIEW PROCESS * Recruiter Interview (30-60 min) * Technical Screening (30 min) * Technical Panel (3x60 min) *This role sits at "PF2" of our framework, please inquire during the recruitment process for further information. At Proxima Fusion, our mission is bold: making limitless clean energy a reality. To get there, we need a high-performing, diverse team that brings different perspectives, challenges assumptions, and builds together with purpose. We know that diversity of thought and experience leads to better ideas, stronger execution, and a more resilient team. We don’t look at how you identify, what you look like, who you choose to worship or what ethnicity you are. We care about what you can bring to the table.
SUMMARY The Plating Engineer will be responsible for the development, optimization, and maintenance of electroplating processes, ensuring high-quality surface finishes on a variety of metal components. This role requires a strong foundation in chemical engineering, materials science, or a related field, as well as hands-on experience with electroplating techniques, process troubleshooting, and laboratory procedures. ESSENTIAL DUTIES AND RESPONSIBILITIES * Design, develop, and improve electroplating processes for various metals (e.g., nickel, gold, silver, chrome, zinc, copper). * Optimized electroless plating processes to improve coating uniformity, reduce chemical consumption, and enhance overall process efficiency and product quality. * Monitor and maintain bath chemistry to ensure optimal plating conditions and consistent product quality. * Conduct root cause analysis and resolve plating defects such as blistering, poor adhesion, thickness, roughness, or discoloration. * Perform routine analytical testing (pH, conductivity, metal concentration, etc.) and adjust chemical compositions accordingly. * Develop and implement standard operating procedures (SOPs) and plating process documentation. * Ensure compliance with environmental, health, and safety regulations related to chemical handling and waste disposal. * Collaborate with R&D, quality control, and production teams to support new product introductions and continuous improvement initiatives. * Specify and help maintain plating equipment, rectifiers, tanks, filters, and agitation systems. * Stay updated on industry best practices, new technologies, and emerging surface treatment techniques. * Uphold Positronic’s standards of integrity, quality, and operational excellence. * Identify hazards in the workplace and report them to management and/or the safety coordinator. * Collaborate with the EHS department to meet local, state, and federal regulatory requirements, including OSHA, NFPA, DNR, EPA, and Amphenol sustainability practices. * Work with the Quality department to ensure compliance with AS9100 certification standards. * Comply with all company policies and procedures. * Perform other duties as assigned. REQUIREMENTS EDUCATION AND EXPERIENCE * Bachelor’s degree in Chemical Engineering, Materials Science Engineering, or related STEM field. * 1 to 2 years of related experience OR an equivalent combination of education and experience. PHYSICAL * Long periods of sitting with occasional standing and walking. * May require bending, kneeling, reaching, pushing, and pulling. * Occasional lifting up to 20 lbs; rarely up to 50 lbs. * Frequent computer use and repetitive motion. * PPE includes safety glasses and gloves when handling chemicals. WORKING CONDITIONS Work is performed in a chemical lab environment with frequent exposure to fumes. Involves small parts handling under magnification. Proper PPE is required. COMPETENCIES KNOWLEDGE * Expertise in electroplating chemistry, process engineering, and quality systems. * Working knowledge of AS9100 standards, SPC tools, and root cause analysis. * Understanding of manufacturing scheduling and cost control. * Knowledge of regulatory compliance in industrial chemical operations. SKILLS * Leadership and team development abilities. * Strong organizational and time management skills. * Skilled in data-driven process evaluation and training implementation. * Effective communicator across technical and non-technical teams. ABILITIES * Leadership and adaptability in a fast-paced environment. * Strong reasoning skills and attention to process variability. * Visual and oral communication clarity for training and coaching. * Time-sharing ability for overseeing multiple plating and lab operations.