Associate Director, Drug Substance
$145k - $207kRelay Therapeutics
The Opportunity:This is a highly visible leadership opportunity to join an attractive discovery-based company that has diverse early and potential late-stage pipeline of drug candidates. In this role you will provide leadership in development and execution of robust and cost-effective processes for new small molecule APIs.Your Role:Manage all late-stage small molecule drug substance development and manufacturing activities at global CRO/CMO sites.Ensure regulatory compliance at vendor site.Lead all late-stage drug substance development efforts toward the commercialization of the small molecule drug candidates.Display the leadership and technical skills necessary to lead the development and manufacturing activities at CRO/CMO sites with minimal supervision. Identify and develop in- process controls for potential commercial process validation. Act as the key technical transfer resource, in implementation of optimized processes on manufacturing scale. Trouble shoot and conduct problem solving of scale-up and manufacturing issues.Review and approve specifications, batch records and other critical documents.Work with other process chemists to support early-stage manufacturing process development/manufacturing and move the project to late-stage development.Collaborate with QC, supply chain and quality assurance to ensure alignment on deliverables.Write and review regulatory documents (NDA and MAA).Your Background:Bachelor or above in chemical engineering/Ph.D. or equivalent in organic chemistry with 7+ years of relevant late-stage Process Development and manufacturing, tech transfer experience in a virtual pharmaceutical industry.Demonstrated ability in late-stage manufacturing process development, validation, and commercial manufacturing at global CMOs in an accelerated environment.Demonstrated ability in cGMP and the development of synthetic methodology and scale-up of new technology.Experience with QbD tools including risk assessment, design of experiments and data analysis, process analytical technologies and their application in identifying CQA, CPP and establishing the appropriate control strategy.Strong outsourcing experience in working with external partners.Analytical skills should include all modern spectroscopic techniques including: NMR experimentation and techniques; IR; mass spectroscopy, ReactIR and UV/Vis; separation techniques including chromatography: HPLC, GC, TLC, flash chromatography, chiral separations and derivitization; solid state characterization; gravimetric analysis and titration.Complete familiarity with the chemical literature and literature searching techniques are required.Strong communication, analytical and problem-solving skills.Good verbal and written communication skills are essential. Strong interpersonal skill set to effectively work with internal and external stakeholders.Knowledge of US FDA and EMEA and ICH guidelines.Work efficiently with multidisciplinary teams within the company and CMO sites.Experience in process validation and NDA or MAA filing is must.Estimated Salary Range: [$145,000 - $207,000].The 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.#BP1About Relay TherapeuticsRelay 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. Our 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!
$145k - $207k
...company that has diverse early and potential late-stage pipeline of drug candidates. In this role you will provide leadership in... ...molecule APIs.Your Role:Manage all late-stage small molecule drug substance development and manufacturing activities at global CRO/CMO sites...Suggested- Xenon Pharmaceuticals is seeking an Associate Director, CMC, Drug Substance to join the CMC Drug Substance team in Boston, MA. The role focuses on overseeing API development and manufacturing programs with CDMOs to support clinical trials and regulatory submissions. The...SuggestedRemote work
- ...neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization... ...operations. _ About the Role: _ We are seeking an Associate Director, CMC, Drug Substance to join our CMC Drug Substance team. The candidate will...SuggestedContract workTemporary workRemote workFlexible hours
$145k - $207k
...Associate Director role leading late-stage small molecule drug substance development and manufacturing at global CMO/CRO sites. Responsible for process development, regulatory compliance, technology transfer, and commercialization support for early and late-stage pipeline...Suggested$152.6k - $283.4k
...Cambridge, MA, USAAbout the RoleWe are seeking an accomplished Associate Director to join our discovery organization and lead scientific... ...approaches. This role is central to advancing differentiated antibody-drug conjugates (ADCs) and related targeted therapeutics by...SuggestedFull time- ...Associate Director role overseeing outsourced manufacturing of oligonucleotide drug substances for clinical and pre-commercial programs. The position requires hands-on expertise in cGMP synthesis and purification, regulatory filing support, and cross-functional collaboration...Contract work
$143k - $203k
Your Role: You will be the lead and an integral part of Relay’s drug product development team supporting development programs.You will be responsible for design, development and optimization of patient-centric (e.g. pediatric) drug product formulation and clinical / commercially...$175k - $201k
...to Our TeamYou are a motivated, resourceful, and enthusiastic Drug Product Development & Manufacturing individual who is excited... ...functional groups and external vendors.The OpportunityThe Associate Director, Drug Product Development & Manufacturing, is accountable for...Work at officeLocal areaRemote work1 day per week$172.2k - $233k
Overview:Alnylam is seeking an experienced leader to serve as Associate Director, CMC Technology Delivery to lead the digital enablement and... ..., and efficient processes across starting material, drug substance and drug product process sciences, analytical sciences, CMC...Full timeContract workTemporary workLocal areaFlexible hours3 days per week$159k - $195k
...individuals, families and communities. Learn more at , and follow us on X, LinkedIn and Facebook.Role Summary:The Associate Director, Formulation and Drug Product Development will be accountable for all internal and external activities related to successful formulation...Local areaRemote work$159k - $219k
About This Role The Associate Director, Small Molecule Analytical Development will provide scientific and people leadership for analytical... ...Lead analytical development activities for small molecule drug substance and drug product programs, including method development, qualification...Full timeContract workTemporary workLocal area$159k - $219k
About This Role The Associate Director, Antisense Oligonucleotide (ASO) Analytical Development will provide scientific and people leadership for analytical development activities supporting ASO drug substance and drug product programs. This role leads the development...Full timeContract workTemporary workLocal area$160k - $240k
...are valued, seen, and heard.How you’ll make an impact:As the Associate Director, Analytical Development, you will contribute to CMC... ...readinessPartner with CMC scientist to understand and characterize drug substance and drug product-related impurities, including impurity...Contract work$94.6k - $141.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced technical resource... ...compliance issues. The role provides Quality oversight for drug substance disposition from development through process performance...Full timeContract workSummer workRemote workFlexible hours2 days per week$185k - $200k
...Development team is seeking an experienced Associate Director of Lipid Process Chemistry to lead the... ...of lipid raw materials into drug product manufacturing. Define and assess... ...regulatory expectations for clinical-stage drug substances. Ideally, you would also have: Prior...Contract workFlexible hours$185k - $225k
...patients suffering from serious diseases.Position Overview:The Associate Director of Product Quality Assurance (PQA) will be responsible for... ...in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and quality. Must...Full timeContract workWorldwide$143k - $233k
Associate Director/Director, CMC Regulatory Cambridge, MA As part of the Pharmaceutical Development... ...medicines company transforming the drug discovery process with the goal of bringing... ...are not limited to: Alcohol or other substance use disorder (not currently using drugs...Contract workFor contractorsFor subcontractorWork at office$158.8k - $238.2k
Job DescriptionGeneral Summary:The Associate Director, QC Technical Services - Small Molecule will lead the technical services group responsible... ...contract testing laboratories performing QC testing of drug substance, drug product intermediate, and drug products, ensuring...Full timeContract workSummer workRemote workFlexible hours2 days per week$152.6k - $283.4k
...MA, USA About the Role We are seeking an accomplished Associate Director to join our discovery organization and lead scientific strategy... .... This role is central to advancing differentiated antibody-drug conjugates (ADCs) and related targeted therapeutics by integrating...- ...Biogen seeks an Associate Director to lead analytical development for small molecule programs from early clinical stages through commercialization... ...through validation, transfer, and lifecycle management for drug substance and product programs Develop phase-appropriate control...Contract work
$135.46k - $203.19k
Job Title: Associate Director, External Quality Location: Boston, MA Hybrid 3 days/week Fusion Pharmaceuticals, a member of the AstraZeneca... ...CDMOs/CMOs, testing labs, and critical suppliers across drug substance, drug product, packaging/labeling, and distribution. Establish...Contract workTemporary work3 days per week$171k - $192k
...Quality Operations team is expanding and looking to hire an Associate Director of Quality Control reporting to the Senior Director of QC/... ...external CMOs and CTLs supporting commercial raw material, drug substance, drug product and finished drug product in-process, release...Contract workLocal areaRemote work$154.4k - $242.55k
...that will inspire you and empower you to shine? Join us as an Associate Director, Tumor Functional Genomics and Perturbation Analytics in our... ...biology, target validation, translational, pharmacology, and drug discovery teams to define scientific questions, design analytical...Minimum wageWork at officeLocal areaRemote work$175.8k - $237.8k
OverviewThe Associate Director, Quantitative Systems Pharmacology (QSP) will support a rapidly expanding clinical portfolio of promising RNAi... ...application of QSP modeling and simulation approaches to answer key drug development questions across the portfolio spanning all...Full timeTemporary workLocal areaFlexible hours$154.4k - $242.55k
...that will inspire you and empower you to shine? Join us as an Associate Director, Tumor Genomics and Targeted Credentialingin our Cambridge... ...biology, target validation, translational, pharmacology, and drug discovery teams to define scientific questions, prioritize analyses...Minimum wageWork at officeLocal areaRemote work$160.8k - $201k
...Skills: Skills and CompetenciesKnowledge of clinical and nonclinical data requirements for product labelingDemonstrated knowledge of drug development process. Knowledge of laws and regulations affecting the pharmaceutical industry, and regulatory experience.Experience...Full time$162k - $270k
...of client deliverables, and maintaining client relationships. Associate Directors oversee multiple projects simultaneously.Common... ...Strong understanding of the pharmaceutical industry, including drug development and launch.· Experience developing, designing, and...Full timeWork experience placementWork at officeRemote workFlexible hours- ...Massachusetts, United StatesCompany: SanofiPosted: 2026-10-24Job title: Associate Director, Global Medical Affairs - DermatologyLocation: Morristown,... ...of gender-neutral parental leaveWork at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital...Local area
$148.5k - $214.5k
Job title: Associate Director - QSP Quantitative Systems PharmacologyLocation: Morristown, NJAbout the JobAt Sanofi, a global health care and... ...and critical decision making throughout the various phases of drug development. The Disease Modeling (DM) group at Sanofi is...Full time$168k - $252k
Job DescriptionGeneral Summary:The Modeling & Simulations Associate Director will be responsible for developing and executing M&S strategies and activities in cross functional drug development project teams in close collaboration with colleagues in Clinical Pharmacology...Full timeSummer workRemote workFlexible hours2 days per week
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