Contract: Manager, CMC Stability Management and Analysis

Immunomeinc; Bothell (WA); On-site; USD 121,366 - 137,828; Part time

Job summary

Immunomeinc, based in Bothell, WA, is seeking a Contract Manager for CMC Stability Management to oversee outsourced stability programs. Candidates should have over 8 years of biopharmaceutical experience and a strong background in GMP stability operations.

This role involves maintaining stability schedules, data reviews, and vendor oversight, focusing on biologics and large-molecule stability requirements. Strong project management and communication skills are essential for collaboration in a dynamic environment.

Qualifications

• 8+ years of experience in stability, QC, or technical operations within biotech.
• Experience managing GMP stability programs for biologics.
• Hands-on with stability data review and trending.

Responsibilities

• Review stability protocols for studies.
• Oversee execution of stability studies.
• Prepare stability summaries and technical assessments.

Skills

GMP stability operations

Biologics knowledge

Project management

Analytical technologies

Education

Bachelor's or advanced degree in Chemistry or related field

Job description

Company Overview

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.

Position Overview

Immunome is seeking an experienced Contract:Manager, CMC Stability Management and Analysis to oversee execution of outsourced stability programs. This contract role will be responsible for maintaining stability pull schedules, data review, and vendor oversight activities across mAb intermediate, drug substance, and drug product.

The successful consultant will bring practical expertise in GMP stability operations, biologics and large-molecule stability requirements, understanding of ADC stability-indicating assays and outsourced laboratory management. This position requires a hands‑on program manager who can translate technical and regulatory expectations into actionable plans, manage timelines and risks across external partners, and ensure stability deliverables are met.

Responsibilities

Study Execution and Operational Oversight

• Review stability protocols for long‑term and accelerated studies.
• Create and maintain stability plans, master schedules, pull calendars, and study trackers across multiple development programs.
• Oversee execution of stability studies and ensure timely sample pulls, testing initiation, data delivery, and escalation of schedule or quality risks.

Data Review, Trending, and Technical Assessment

• Review stability data for completeness, accuracy, data integrity, trend behavior, specification compliance, and consistency with expected product quality attributes.
• Support evaluation of OOS/OOT results and atypical trends.
• Prepare stability summaries, trend reports, shelf‑life assessments, retest/expiry recommendations, and technical risk assessments to support program decision‑making.

Qualifications

• Bachelor’s or advanced degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related field.
• 8+ years of experience in stability, QC, Analytical Development, CMC, or technical operations within the biotechnology or biopharmaceutical industry, or equivalent.
• Demonstrated experience managing GMP stability programs for biologics, monoclonal antibodies, fusion proteins, or other large molecules; ADC experience preferred.
• Hands‑on experience with stability data review, trending, shelf‑life assessment.
• Prior experience managing external CTLs, CDMOs, CROs, or stability storage vendors supporting regulated studies.
• Working knowledge of GMP requirements, data integrity expectations, ICH stability guidance, and regulatory expectations for biologics stability studies.
• Contract or consultant experience in a matrixed biotech environment preferred.

Knowledge and Skills

• In‑depth understanding of biologics stability program management, including drug substance and drug product stability, retest/expiry dating, storage condition justification, and ongoing stability commitments.
• Working knowledge of ICH Q1A(R2), Q1B, Q1D, Q1E, Q5C, relevant FDA/EMA expectations, and phase‑appropriate application of stability requirements.
• Strong understanding of biologics product quality attributes.
• Familiarity with analytical technologies used in biologics stability testing, including HPLC/UPLC, SEC, CE‑SDS/cIEF/icIEF, ELISA, binding and potency assays.
• Strong project management skills with the ability to manage detailed schedules, multiple vendors, cross‑functional dependencies, and competing program priorities.
• Ability to interpret stability trends, identify risks, escalating issues appropriately, and drive practical solutions in collaboration with technical and quality stakeholders.
• Excellent documentation, communication, and stakeholder management skills.
• Comfort with ambiguity and dynamic timelines; ability to operate independently and drive execution with limited supervision.

Compensation

WA State Contract Pay Transparency (Hourly Rate) $88.10 — $100.05 USD

E/E/O

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

E-Verify

Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster (English) | Right to Work Poster (English) | Right to Work Poster (Spanish).