Director, Analytical Development and Quality Control

Relay Therapeutics•Cambridge, MA

1d•$160,000 - $228,000

About The Position

We are seeking a highly motivated and strategic leader to direct analytical development and quality control strategies in support of drug substance and drug product development across all stages of development. In this role, you will establish and lead the analytical strategy for our small molecule programs and serve as a key partner across CMC, Regulatory, and Quality functions. You will work closely with internal stakeholders and external partners, including CMOs and CROs, to ensure robust analytical methods and quality systems are implemented to support development, manufacturing, and regulatory submissions. This is a highly visible leadership role with responsibility for shaping analytical strategies that enable the successful advancement of our clinical pipeline.

Requirements

You have earned an MS or PhD in Analytical Chemistry, Biochemistry, Biotechnology, or a related discipline, with 10+ years of industry experience, including significant experience leading analytical development activities in a pharmaceutical or biotechnology environment.
You have deep expertise in analytical development, method validation, technology transfer, troubleshooting, and quality control for small molecule drug development.
You have experience developing analytical strategies across multiple phases of development, including IND-enabling and late-stage programs.
You possess strong technical expertise in analytical methods for small molecule drug substances and oral solid dosage forms.
You are an effective communicator who can collaborate successfully with cross-functional internal teams, contract laboratories, and manufacturing partners.
You are comfortable managing multiple programs and priorities in a dynamic development environment.

Nice To Haves

Experience supporting regulatory filings (IND, NDA, or equivalent) and interacting with global regulatory agencies such as the FDA, EMA, or PMDA is strongly preferred.

Responsibilities

Setting and executing the analytical development and quality control strategy across our development programs, ensuring phase-appropriate analytical methods and control strategies are in place to support drug substance (DS) and drug product (DP) development.
Leading analytical method development, validation, and lifecycle management activities required for the full characterization of small molecule NCEs.
Providing scientific and strategic oversight of external laboratories, CMOs, and CROs conducting analytical development, method validation, release testing, and stability testing in support of Relay clinical candidates.
Reviewing and approving analytical development strategies, method transfer and validation protocols, datasets, and final reports.
Overseeing QC testing performed at external analytical laboratories and DS/DP manufacturing sites to ensure compliance with cGMP standards.
Providing quality oversight and approval of cGMP QC documentation, including change controls, deviations, CAPAs, analytical procedures, and validation protocols.
Reviewing analytical data packages and raw data from third-party laboratories to support batch disposition and release.
Overseeing the Reference Standard program, including establishing and maintaining reference standards, approving qualification protocols and reports, and coordinating release testing at external laboratories.
Leading activities related to critical quality attributes (CQAs), specifications, stability strategies, data trending, shelf life determinations, and expiry dating for drug substance and drug product.
Defining and implementing phase-appropriate analytical and stability strategies across all clinical development programs.
Authoring and reviewing QC and analytical sections of regulatory filings, including INDs and NDAs, and provide technical leadership for responses to Health Authority questions.
Representing the analytical function in cross-functional program teams and contribute to overall CMC strategy and regulatory planning.
Building strong partnerships across Regulatory Affairs, CMC, Quality Assurance, and external partners to ensure alignment on development and regulatory strategies.
As the analytical function grows, you may mentor and lead internal scientists or matrix teams, while establishing scalable processes and best practices.