Principal Scientist Analytical Development & Quality Control, Small Molecule

Retro•Redwood City, CA

2d•$185,000 - $225,000•Remote

About The Position

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to broadly improve tissue function by targeting mechanisms of aging with the ultimate aim of adding 10 years to healthy human lifespan. We’re building a mission-driven team of accomplished and kind individuals who embrace our startup culture of rapid iteration, transparency, and versatility. About the Role: We are seeking a new member of the Quality and Analytical team to support Retro’s clinical-stage autophagy program through Analytical Development (AD) and Quality Control (QC) as it advances from Phase I toward Phase II development. As the primary AD/QC scientist for our small molecule program, you will lead the analytical strategy for drug substance and drug product, working closely with the Program Lead, CMC Lead, QA, and external CDMOs and CROs. You will help ensure product quality, support manufacturing and regulatory activities, and strengthen the analytical foundation needed for continued clinical development. Your responsibilities will include analytical method development, qualification, validation, transfer, specification setting, stability studies, impurity characterization and control, formulation support, regulatory documentation, and oversight of outsourced analytical and QC activities. You will also perform targeted hands-on laboratory work to support development, characterization, troubleshooting, and comparability assessments. Experience with LC-MS and other mass spectrometry-based techniques will be valuable. This role reports to the Head of Quality & Analytical and partners closely with the CMC Lead to execute the analytical and quality strategy for Retro’s small molecule program.

Requirements

7+ years of experience in small molecule analytical development, or related pharmaceutical development work in a regulated environment.
Understand phase-appropriate analytical control strategy, including specifications, stability strategy, impurity control, reference standards, method validation, and regulatory documentation.
Have experience developing, validating, transferring, or overseeing analytical methods for drug substance and drug product release, stability, dissolution, and impurity testing.
Have experience working with CDMOs, CROs, or external laboratories to manage analytical development, validation, release testing, stability testing, investigations, and data review.
Bring hands-on expertise with UPLC/HPLC method development, troubleshooting, and data interpretation for small molecule assay, purity, impurities, degradation products, and related substances.
Can operate independently in a lean environment, prioritize across internal hands-on work and external partner oversight, and communicate analytical recommendations clearly to cross-functional partners.
Hold an advanced degree in analytical chemistry, chemistry, pharmaceutical sciences, medicinal chemistry, or a related scientific discipline, or bring equivalent industry experience.

Nice To Haves

Experience with small molecules that present solubility, dissolution, bioavailability, manufacturability, or product performance challenges.
Experience designing or overseeing forced degradation studies, degradation pathway characterization, and stability-indicating method development.
Experience with extractables and leachables assessments, container closure compatibility, administration-device compatibility, or material compatibility studies.
Supported or authored analytical sections of CTD Module 3 regulatory submissions.
Experience applying analytical methods to research-stage small molecule analogue screening, compound characterization, or compound progression decisions.
Hands-on experience with LC-MS or other mass spectrometry-based approaches for compound characterization, impurity identification, degradation pathway assessment, or analytical comparison of small molecule analogues.
Worked in a startup or resource-constrained environment where scientific independence, adaptability, and strong judgment were essential.

Responsibilities

Drive analytical control strategy development for Retro’s small molecule autophagy program, including drug substance and drug product methods, specifications, stability, impurity control, and regulatory support.
Oversee outsourced QC and characterization methods, including method development, validation, release testing, stability testing, analytical investigations, and data package review.
Support formulation development by using analytical data to help evaluate solubility, dissolution, stability, manufacturability, and overall product performance.
Identify analytical, formulation, vendor, or regulatory risks early and drive practical remediation plans in partnership with Q&AD, CMC, Quality, Regulatory, Research, and external partners.
Author and review analytical sections of regulatory submissions, including Module 3 content related to analytical methods, specifications, validation, stability, and control strategy.
Support identity testing strategy for critical raw materials, including method selection, vendor coordination, data review, and targeted in-house analytical work where appropriate.
Provide UPLC-based analytical support for research activities where appropriate, helping generate data that informs analogue characterization, compound selection, and progression decisions.