Senior Level Quality Control Engineer Jobs
Senior level quality control engineer jobs put experienced engineers in charge of quality systems, compliance strategy, and the cross-functional teams and initiatives that keep production and product integrity on track. Openings concentrate in Consulting & Professional Services, Construction & Real Estate, and Biotechnology & Pharmaceuticals, with 13% of roles offered remotely or hybrid, and employers like Garver, Jobot, and Redwood Materials hiring at this level now.
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INTRODUCTION
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
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 ensuring 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.
COMPENSATION
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.
Base Pay Salary Range: $164,000 - $205,000 USD
Our compensation package 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.
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.
INTRODUCTION
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide. Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
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 ensuring 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.
COMPENSATION
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.
Base Pay Salary Range: $164,000 - $205,000 USD
Our compensation package 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.
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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Senior Level Quality Control Engineer Jobs: Frequently Asked Questions
How do I get a senior level quality control engineer job?
Employers at this level want candidates who can own quality programs end-to-end, not just execute tasks. Highlight experience leading audits, writing or revising quality management systems, mentoring junior engineers, and driving corrective action processes across departments. Demonstrable outcomes, such as defect rate reductions or successful regulatory audits, carry more weight than titles alone. Certifications like CQE or ASQ credentials strengthen your candidacy significantly.
Which companies hire senior level quality control engineers?
Companies hiring senior level quality control engineers right now include Garver, Jobot, and Redwood Materials, based on current listings on Migrate Mate as of November 2026. Hiring at this level tends to come from manufacturers, defense contractors, medical device companies, and aerospace firms with mature quality systems that require experienced leadership to maintain and improve.
Are there remote senior level quality control engineer jobs?
Yes, though many roles require at least some on-site presence given the hands-on nature of quality oversight. About 13% of senior level quality control engineer openings are remote or hybrid as of November 2026, with fully remote positions more common in quality systems, documentation, supplier quality, and audit coordination than in production-floor roles.
What makes a quality control engineer role senior level?
Senior level quality control engineer roles are defined by ownership and scope. Where mid-level engineers execute inspection plans and report findings, senior engineers design the systems, set quality standards, lead cross-functional corrective action teams, and mentor junior staff. They are accountable for regulatory compliance outcomes, supplier qualification programs, and often serve as the primary point of contact during customer or third-party audits.
Which industries hire the most senior level quality control engineers?
Senior level quality control engineer roles concentrate in Consulting & Professional Services, Construction & Real Estate, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they operate under strict regulatory frameworks, complex supply chains, or safety-critical production environments where experienced quality leadership is essential rather than optional.