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Pharmaceutical Stability Jobs (NOW HIRING)

Pacelabs

PLS GMP Stability Coordinator

Oakdale, MN · On-site

$60K - $70K/yr

This is a full-time, onsite, GMP Stability Coordinator position located in Oakdale, MN,Monday ... pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO ...

Pace

PLS GMP Stability Coordinator

Oakdale, MN · On-site

$60K - $70K/yr

This is a full-time, onsite, GMP Stability Coordinator position located in Oakdale, MN, Monday ... pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO ...

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How much do pharmaceutical stability jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for pharmaceutical stability in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a Pharmaceutical Stability job?

A Pharmaceutical Stability job involves evaluating the shelf-life and storage conditions of drug products to ensure their potency, safety, and efficacy over time. Professionals in this role conduct stability studies, analyze degradation patterns, and follow regulatory guidelines set by agencies like the FDA and ICH. They work closely with quality control, regulatory, and formulation teams to support product development and approval.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Stability position, and why are they important?

To thrive in Pharmaceutical Stability, you need a solid background in pharmaceutical sciences or chemistry, strong analytical abilities, and attention to detail, often underpinned by a bachelor’s or master’s degree in a relevant field. Familiarity with laboratory instrumentation (such as HPLC, GC, and dissolution testers), GMP regulations, and data management systems is essential. Strong organization, problem-solving skills, and effective teamwork and communication abilities set outstanding professionals apart. These skills ensure accurate stability testing, regulatory compliance, and successful collaboration within cross-functional teams in pharmaceutical development.

What are the typical daily responsibilities of someone working in Pharmaceutical Stability?

Professionals in Pharmaceutical Stability are primarily responsible for designing, executing, and documenting stability studies to ensure the quality and shelf-life of pharmaceutical products. Their daily tasks often involve preparing samples, conducting analytical tests using specialized lab equipment, recording data, and interpreting results in accordance with regulatory guidelines. They also collaborate regularly with formulation scientists, quality assurance teams, and regulatory affairs to support product development and submission activities. Attention to detail, adherence to standard operating procedures, and clear communication are essential parts of the job.

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Pharmaceutical Stability jobs near you
Infographic showing various Pharmaceutical Stability job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $41,139 per year, or $19.8 per hour.
Director, Stability Management, Analytical Development and Quality Control

Director, Stability Management, Analytical Development and Quality Control

Revolution Medicines

Redwood City, CA • On-site

Full-time

Re-posted 21 days ago

Job description

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.
The Opportunity:
Playing a critical role as the stability program lead, the position will be responsible for oversight and management of outsourced stability studies conducted. The director, stability is a self-motivated individual who works as a member of an integrated team contracting, designing, managing, and evaluating stability studies at contractors for both drug substance and drug product. This individual should have the breadth of experience required to manage stability studies in commercial, late and early clinical development stage. This individual should have broad knowledge of ICH and cGMP guidelines and the ability to contribute to global regulatory filings for stability.
  • Develop and implement the strategic direction of stability programs in alignment with ICH guidelines and regulatory expectations.
  • Oversee the design, execution, and management of stability studies (development, registration and commercial).
  • 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 contractors.
  • Serve as the primary point of contact for contract organization for all stability related activities.
  • Oversee sample shipment if applicable, 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.
  • Drive continuous improvement of stability management processes, including contract organization performance metrics.
  • Collaborate cross-functionally with teams in drug substance, drug product, supply chain, quality, regulatory, sourcing and other related team to ensure alignment of stability design and achieve stability study objectives.

Required Skills, Experience and Education:
  • PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 12+ years of industry experience; or MS with 15+ years, or BS with 18+ years.
  • 10+ 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-Hybrid #LI-CT1

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.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$211,000-$264,000 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 careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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