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Relay Therapeutics

Associate Director, Drug Substance

Relay Therapeutics is hiring an Associate Director, Drug Substance in Cambridge, United States. It pays $145k-$207k a year and Level rates it ; you can apply on Level.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include Hplc, Gc and Tlc.
  • Level files it as a lead role.
  • Level lists 15 other open roles at Relay Therapeutics.
  • The role was posted within the past week.

AI in this role

Lead late-stage small molecule drug substance development, manufacturing activities, and technical transfers at global CRO/CMO sites.

hplcgctlcnmrir
process-developmentchemistrymanufacturingregulatory-compliancequality-assurance

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.

#BP1

About Relay Therapeutics

Relay 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! 

 

 

How we rate this

Associate Director, Drug Substance at Relay Therapeutics rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Process DevelopmentChemistryManufacturingRegulatory ComplianceQuality AssuranceHplcGcTlc

Questions you could be asked

  1. Tell me about a project where process development was part of your work. What did you do?
  2. Tell me about a project where chemistry was part of your work. What did you do?
  3. Tell me about a project where manufacturing was part of your work. What did you do?
  4. Tell me about a project where regulatory compliance was part of your work. What did you do?
  5. Tell me about a project where quality assurance was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Process Development, Chemistry, Manufacturing, Regulatory Compliance, and Quality Assurance. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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