Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.
We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
Key Accountabilities/Core Job Responsibilities:
Ensure effective and efficient completion of key technical deliverables including Quality Agreements, batch record review, method validation
Accountable for developing collaborative and productive partnerships across Denali as well as external contract manufacturing organizations, study site pharmacies, and QPs
Identify & mitigate GMP risks
Oversee the Quality Management System and modify & develop as needed to meet the growing needs of the organization
Support investigational new drug applications (IND), ex-US clinical trial applications (CTA), new drug applications (NDA/BLA/MAA) and related correspondence from the US Food and Drug Administration (FDA) and other global regulatory authorities
Manage internal and external audits
Partner with external vendors in support of Quality document preparation and submission
Maintain up-to-date knowledge of the Quality landscape, regulations, and guidelines
Support development of specifications for biologics and small molecule programs
Ensure compliance with relevant governing laws, regulations, guidelines, and Denali SOPs
Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.
Qualifications/Skills:
20+ years relevant experience in GMP Quality or relevant functions, and experience in both biologics and small molecule quality is highly desirable and 15+ years of management experience
Bachelor’s degree required, and advanced scientific degree desirable
Broad understanding of international regulations and guidance
Strong experience in IND and CTA filings. NDA/BLA/MAA experience strongly preferred
Experience in auditing CMOs and managing internal audits desirable
Excellent written and verbal communication skills
Exceptional influencing, partnership, and collaboration skills
Strong ability to prioritize workload and manage the growth & development of employees
Well-prepared, competent, and confident when interacting with senior management, health authorities, and internal and external partners
Able to prospectively identify potential problems and to partner effectively and positively to solve issues
This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.
Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.