Revolution Medicines

Senior Manager, Stability Management, Analytical Development and Quality

Revolution Medicines$164K — $205K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years.
  • 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 organizations and working in a virtual development model.
  • Excellent leadership, project management, and collaboration skills.
  • Strong problem-solving skills with strategic decision-making ability.
  • Excellent written and verbal communication and interpersonal skills.

Responsibilities

  • Coordinate stability activities including monitoring schedules and data review.
  • Track stability studies and maintain the stability database.
  • Author and review stability-related documents such as protocols and reports.
  • Collaborate cross-functionally with CMC, quality, regulatory, and clinical teams.
  • Compile stability study results and prepare reports for regulatory support.
  • Partner with quality on stability quality events and investigations.
  • Manage sample shipment and inventory tracking for stability studies.

Benefits

  • Competitive cash compensation and robust equity awards.
  • Strong benefits package including health, dental, and vision coverage.
  • Significant learning and development opportunities.
  • Flexible work environment with hybrid options.
  • Supportive, energetic, and team-oriented company culture.
Full Job Description
The Opportunity:

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

Required Skills, Experience and Education:
  • PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years.
  • 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.
  • Excellent leadership, people/team management, project management, and cross-functional collaboration skills.
  • Strong problem-solving skills with strategic and technically sound decision-making ability.
  • Excellent written and verbal communication skills and interpersonal skills.
  • Energetic, team-oriented, and adaptable to a fast-paced, dynamic environment.

Preferred 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. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Base Pay Salary Range

$164,000-$205,000 USD

We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

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. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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