<div>Company introduction: 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. - <a href="https://compasspathways.com/">Compass Pathways</a>.</div>Job overview:   The Technical Writer, CMC will be responsible for document writing, authoring, and compiling of CMC reports and the CMC sections for regulatory (NDA) filings. This position will work closely with the cross-functional teams within Quality, Clinical and Regulatory Affairs to ensure all CMC technical writing objectives are met.  Location: Hybrid in our New York City office or remote on the East Coast, USA. Reports to: Vice-President, Manufacturing and Supply.   Roles and responsibilities  (Include but are not limited to):  <ul> <li>Author and/or review technical reports as required by CMC staff</li> <li>Author, compile, and manage CMC sections of regulatory submissions (IND/NDA)</li> <li>Effectively manage the integrated drafting and reviewing process to meet appropriate timelines</li> <li>Ensure all documents comply with regulatory guidelines, company standards, and industry best practices</li> <li>Work closely with cross-functional teams to gather input and feedback for report content and formatting</li> <li>Organize and maintain document storage to ensure easy access to reports and related documentation</li> </ul> Candidate Profile: <ul> <li>Minimum of bachelor’s degree in chemical, and/or, biological Sciences/relevant discipline</li> <li>Over 3 years experience in technical writing for CMC regulatory filings (especially NDA)</li> <li>Strong working knowledge of full CMC spectrum, including drug substance and drug product manufacturing, stability requirements, analytical and formulation development and GMP manufacturing considerations in general</li> <li>Knowledge of FDA, EMA and global regulations including ICH guidelines with a strong knowledge of eCTD elements and structure</li> <li>Demonstrated ability to translate technical information from mixed sources into written information suitable for regulatory authorities</li> <li>Excellent verbal/written communication skills; detail/accuracy oriented</li> <li>Proven planning and organizational skills and regulatory writing skills</li> <li>Ability to work independently in a fast-paced environment with demonstrated ability to simultaneously manage multiple competing demands</li> </ul><div><div><div>【For NYC】Compensation Description (annually): Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location. Base pay is one part of the Total Package that is provided to compensate and recognise employees for their work and any role at Compass, regardless of the location, is eligible for additional discretionary bonuses and equity.</div><div>【Base salary per annum】:</div><div>$120,000—$170,000 USD</div></div></div><div><h2>Benefits &amp; Compensation:</h2> For an overview of our benefits package and compensation information, please visit  <a href="https://compasspathways.com/join-us/">Working at Compass</a>.   <h2>Equal opportunities:  </h2> 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. <h2>Sponsorship:</h2> Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying. <h2>Data Privacy:</h2> All data is confidential and protected by all legal and data privacy requirements, please see our recruitment <a href="https://compasspathways.com/recruitment-candidates-privacy-notice/" target="_blank">Privacy Notice</a> to learn more about how we process personal data.</div>

COMPASS Pathways

Technical Writer, CMC

COMPASS Pathways