Revolution Medicines

Senior Manager, Stability Management, Analytical Development and Quality

Redwood City, California, United States · Senior · Full-time

Sponsorship not specified$164k-$205kDetected 23 hours ago

ComplianceProject ManagementAR/VRGMPFDA RegulatoryLeadershipCommunicationCollaborationProblem SolvingPublic SpeakingAdaptability

About the role

Coordinate stability activities, including but not limited to monitor schedule, data entry, review and presentations/reports.
Work cross functionally with CMC, quality, regulatory, clinical and related teams to achieve stability objectives.
Playing a critical role as the subject matter expert (SME) on stability management, the position will be responsible for management of outsourced stability studies.

Compile stability study results, perform trend and statistical analyses, and prepare reports to support retest/shelf-life date extensions and storage condition recommendations.
Partner with quality during stability quality events (QEs) or investigations and implementation of CAPAs at contract organization.
Manage sample shipment, inventory tracking, and chain of custody for stability studies.
Support, author CMC stability documentation for IND, NDA, AR and IMPD filings, covering all phases of clinical development and commercial activities by ensure completeness and accuracy of stability data.
Manager, stability is a self-motivated individual who works as a member of an integrated team from design, management, and evaluation stability studies outsourced to contract organization.

PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience
or MS with 10+ years, or BS with 12+ years.
This individual should have the breadth of experience and knowledge required to support commercial, late and early clinical development stage.
This individual should have good understanding of ICH and cGMP guidelines and the ability to contribute to global regulatory filings for stability.

6+ years in stability management or relevant experience within pharmaceutical or biotech industry.
Strong knowledge of GMP regulations, quality systems, ICH guidelines, and regulatory expectations (FDA, EMA, etc.).
Extensive experience managing contract organization and working in a virtual development model.
Strong problem-solving skills with strategic and technically sound decision-making ability.
Excellent written and verbal communication skills and interpersonal skills.
Experience with small molecule oncology drug development.
#LI-CT1 #LI-Hybrid
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below.

$164,000 - $205,000 USD
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process.

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers.
The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins.
The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

This listing is sourced directly from Revolution Medicines's careers page and normalized into a canonical job model.