{"id":1322989,"url":"https://alion.io/job/relay-tx-associate-directordirector-cmc-regulatory","title":"Associate Director/Director, CMC Regulatory","company":{"id":3232729,"name":"Relay Therapeutics","domain":"relaytx.com","url":"https://alion.io/company/relaytx","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"head","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Cambridge, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":143000,"max":233000,"currency":"USD","period":"year","gross":null,"usd_annual":233000},"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-10T18:49:25Z","employer_posted_date":"2026-09-10","last_verified_at":"2026-10-20T10:43:22Z","board_verified":true,"closed_at":null,"days_open":39,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":39},"description":"As part of the Pharmaceutical Development team, this position will play a key role in regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) programs. \nYour Role: \nWith minimal supervision, accountable for developing and leading the execution of regulatory CMC investigational, registration and/or post-approval strategies for Relay's development programs/products.\nDevelop and execute CMC global submission plans and timelines in accordance with project goals\nStrong and deep foundational understanding of global RA CMC regulations and guidelines.\nApply and adapt this understanding to projects to enhance probability of regulatory success and regulatory compliance.\nAbility to draw from prior experience, precedents and other regulatory intelligence beyond regulations. Strong analytical or process understanding that enables the development of robust and accurate submissions.\nApply global regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization.\nResponsible for leading and coordination of responses to CMC questions/RFIs from regulatory authorities in conjunction with CMC and regulatory affairs leads/SMEs.\nIndependently defines CMC content (data and documentation) requirements for regulatory submissions and reviews this content for conformance with established requirements.\nResponsible for CMC-regulatory activities listed above with cross-functional teams and act as the regulatory CMC liaison between CMC/PD, regulatory affairs and/or program management, as applicable.\nLead and manage CMC-regulatory assessment and guidance on product compliance topics, including change controls, deviations, and GMP investigations, as applicable, in conjunction and consultation with CMC leadership.\nProactively communicates CMC regulatory strategies, key issues and risks through assigned programs / products development activities and LCM in adequate and timely manner to cross-functional programs/ products teams and management level within PharmDev and Regulatory Affairs Teams, as appropriate.\nKeep abreast of regulatory guidance and technical/scientific developments relevant to projects.\nCompetencies:\nStrong background in CMC-regulatory affairs with focus on small molecule (preferably solid orals: tablets, capsules) clinical (IND/IMPD) and/or commercial (NDA/MAA) submissions.\nProven ability to lead and manage regulatory CMC projects independently. Able to deal with issues of critical importance with minimal supervision. Exercises good judgement in elevating and communicating actual or potential issues to line management.\nIn-depth knowledge of global CMC regulatory requirements and guidelines (e.g. FDA, EMA, ICH).\nPositive attitude, energetic and proactive.\nStrong technical writing and document review skills.\nExcellent organizational skills, ability to multi-task and prioritize assignments, operational creativity, strong problem-solving skills, self-motivated and able to work under pressure.\nStrategic thinking capabilities with forward looking perspective and ability to find solutions, in alignment with management and program goals, strong communication, planning, and collaboration skills\nAttention to detail, follow-up/through skills; ability to work individually and within multi-disciplinary internal and external teams at third parties.\nAbility to effectively manage multiple projects with competing priorities.\nYour Qualifications:\nBachelor or advanced degree in Pharmaceutical Sciences, Chemistry or related fields.\nMinimum of 8-10+ years of relevant experience in regulatory-CMC and/or within CMC function (e.g. analytical, formulation and process development, QA, QC) in the biotech/pharmaceutical industry with a focus preferably on CMC for small molecules and oral solid products.\nExperience with authoring/review/providing CMC content for CMC/quality submissions including IND and IMPD development/maintenance.\nKnowledge of eCTD Modules and QOS requirements for INDs/IMPDs and NDAs/MAAs.\nExperience managing submissions in RIM Veeva or equivalent; document formatting/Quality Control compliant with eCTD templates / requirements.\nEstimated Salary Range: [$143,000 - $233,000].\nThe range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.\nAbout Relay Therapeutics\nRelay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process. \nOur team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!","description_format":"text","description_chars":5635,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Drug Discovery"],"lifecycle":[{"event":"open","at":"2026-09-26T23:32:10Z"}],"visa":[],"liveness":{"score":37,"band":"fade","label":"Fading","p_open":1,"p_active":0.677,"p_room":0.55,"age_days":39,"expected_fill_days":27,"reasons":["conf:0","win:tail"],"computed_at":"2026-10-20T05:45:00Z"},"pay":{"stated_usd_annual":233000,"is_top_pay":false},"html_url":"https://alion.io/job/relay-tx-associate-directordirector-cmc-regulatory","json_url":"https://alion.io/job/relay-tx-associate-directordirector-cmc-regulatory.json","meta":{"generated_at":"2026-10-20T14:40:05Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":16495,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-21T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":3232729},"rest":"https://alion.io/mcp/rest/get_company?id=3232729"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Frelay-tx-associate-directordirector-cmc-regulatory"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Frelay-tx-associate-directordirector-cmc-regulatory"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Frelay-tx-associate-directordirector-cmc-regulatory"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/relay-tx-associate-directordirector-cmc-regulatory\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Frelay-tx-associate-directordirector-cmc-regulatory"}]}