About this opportunity
Glaukos Corporation lists this Pharmaceutical/Biologics R&D Quality Lead opportunity in aliso viejo, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Glaukos – Pharmaceutical/Biologics R&D Quality Lead
Location: Aliso Viejo, CA
How Will You Make an Impact?
The R&D Quality Lead, Pharma/Biologics will play a key role in advancing quality strategy and supporting the successful development of pharmaceutical, biologic, and combination products. This position serves as a trusted quality partner across research, development, regulatory, clinical, and manufacturing functions, helping ensure compliance, product quality, and operational excellence throughout the product lifecycle. The role also serves as the primary Quality liaison for external development and manufacturing partners.
What Will You Do?
Serve as the GMP and R&D Quality subject matter expert for pharmaceutical, biologic, and combination product development programs.
Provide quality oversight for outsourced development and manufacturing activities, including drug substance, drug product, biologic intermediates, clinical trial materials, analytical development, validation, manufacturing, packaging, labeling, release, and stability programs.
Partner with cross-functional teams to provide quality input into product development plans, technology transfer activities, validation readiness, supplier oversight, and commercialization efforts.
Review and approve development and validation protocols, reports, specifications, analytical methods, batch documentation, release records, and CMC documentation.
Support and maintain phase-appropriate GMP quality systems, including change control, deviations, CAPA, supplier quality management, training, documentation control, and data integrity programs.
Ensure quality documentation complies with company standards, industry regulations, and global regulatory expectations.
Provide quality review and support for regulatory submissions, including investigational applications, marketing applications, annual reports, and regulatory updates.
Participate in audits, inspections, and cross-functional project teams to drive continuous improvement and compliance excellence.
Communicate project progress, risks, and recommendations to leadership and key stakeholders.
How Will You Get Here?
Education
Bachelor's degree in a scientific discipline such as Biology, Chemistry, Pharmacy, Engineering, Mathematics, or a related field required.
Master's degree preferred.
Experience
12+ years of pharmaceutical, biologic, or combination product industry experience, or 8+ years with a Master's degree.
Strong experience in R&D Quality, CMC, GMP compliance, clinical supply, supplier oversight, and regulatory submission support.
Demonstrated experience supporting pharmaceutical and biologic product development programs.
Experience applying GMP and regulatory requirements in development or manufacturing environments.
Knowledge of FDA, EMA, ICH, and global GMP regulations.
Understanding of validation principles for pharmaceutical manufacturing, testing, and equipment systems.
Familiarity with global CMC development and regulatory filing processes.
Strong project management, communication, and stakeholder management skills.
Audit experience and supplier quality oversight experience preferred.
Ability to effectively manage multiple priorities and navigate complex quality and compliance challenges in a fast-paced environment.
Why Join Glaukos?
At Glaukos, you'll have the opportunity to contribute to innovative therapies that improve patient outcomes while partnering with talented teams across research, development, clinical, regulatory, and manufacturing functions. This role offers the chance to make a meaningful impact on the development of next-generation pharmaceutical and biologic products in a collaborative, mission-driven environment.
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Worksite address
aliso viejo, CA, 92656, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.