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Relay Therapeutics

Drug discovery platform targeting protein motion

Associate Director - Drug Product

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeCambridge, MA, USA$143k - $203kIn-person

About the Job

Requirements

  • An advanced doctoral or post-doctoral degree in Pharmaceutics, Pharmaceutical Sciences, or a related field, and at least 8 years of relevant industry experience, with a proven track record in oral solid formulations, liquid suspension formulations, and manufacturing process development, optimization, and scale-up.
  • Understanding of the fundamentals of pediatric product development, including selection of excipients, dosage forms, and packaging configurations for pediatric populations.
  • A strong understanding of phase-appropriate immediate-release oral formulations, manufacturing process development, and the overall pharmaceutical product development process.
  • Experience identifying critical process parameters, defining design space, applying design of experiments, and using statistical programs commonly used in the pharmaceutical industry.
  • Knowledge of current Good Manufacturing Practices and experience developing new chemical entities under cGMP.
  • Knowledge of CMC quality guidelines relevant to oral solid drug product development, particularly US, EU, Japanese, and ICH guidelines.
  • Ability to author and review technical reports supporting IND/NDA submissions, regulatory compliance, and intellectual property requirements.
  • Ability to think strategically and find solutions aligned with management and program goals.
  • Ability to work independently and within multidisciplinary internal and external teams.

Responsibilities

  • Lead and contribute to Relay’s drug product development team in support of development programs.
  • Design, develop, and optimize patient-centric drug product formulations, including pediatric formulations, and clinically and commercially viable manufacturing processes; select appropriate packaging and container closure systems for pipeline products.
  • Lead and manage outsourced formulation, product development, and manufacturing activities at global CRO/CMO sites in alignment with program goals.
  • Manage prototype development, feasibility assessments, and clinical manufacturing activities.
  • Support current and planned formulation and drug product research and development, as well as Good Manufacturing Practice stability studies, in collaboration with internal analytical development, quality control, and quality assurance teams and third parties.
  • Serve as a drug product subject-matter expert for technology transfer of drug product processes to manufacturing sites, providing technical input and insights to contract manufacturing organizations.
  • Draft, review, and approve specifications, batch records, and other critical development and GMP documents.
  • Author and review drug product sections of CMC regulatory submissions, including IND, IMPD, NDA, PIP, iPSP, and briefing packages; respond to regulatory questions and provide supporting documentation in a timely manner.
  • Contribute to cross-functional teams and collaborate to meet program and project objectives and key results.
  • Evaluate and implement new and sustainable drug product technologies for pipeline products and lifecycle management, as applicable.
  • Plan and prioritize assignments, multitask, and solve operational problems while working under pressure.

Desired Qualifications

  • Experience with palatability assessment, taste masking, and in-use stability and food compatibility.

About the Company

Relay Therapeutics

Drug discovery platform targeting protein motion

Relay Therapeutics uses its Dynamo platform to discover drugs by exploring how proteins move, enabling them to target proteins previously considered undruggable. The platform blends experimental data with computational modeling to identify and optimize therapeutic candidates, with a focus on precision oncology and genetic diseases. Its approach combines motion biology, data-driven design, and active partnerships (such as a worldwide license and collaboration with Genentech) with an internal drug pipeline. The company aims to bring life-changing medicines to patients by advancing clinical trials and securing licensing collaborations to fund and validate its therapies.

Company size
201-500
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2016

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