Associate Director, QC for QA
Associate Director, QC for QA
Denali Therapeutics
South San Francisco, CA
See who Denali Therapeutics has hired for this role
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.
Responsibilities (include But Are Not Limited To The Following)
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.
Applicant Privacy Policy
https://www.denalitherapeutics.com/denali-applicant-privacy-policy
We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
Responsibilities (include But Are Not Limited To The Following)
- Provide Analytical and QC Subject Matter Expertise within the Quality Group.
- Oversee GMP Quality operations at CMOs, with a focus on QC activities, including quality documentation reviews and approvals and assisting the disposition of Denali products.
- Support PPQ activities which will include review of process validation protocols/reports, risk assessments, method validation protocols and all associated reports.
- Write Quality documentation including specifications, SOPs and Policies.
- Support supplier qualification and quality audits for Denali sites including CMOs/CTLs as needed.
- Oversee product quality aspects of the supply chain and distribution networks.
- Establish and support quality systems and operations, including document control, change controls, deviation, CAPA, effectiveness checks and temperature excursions.
- Improve quality processes and systems and seek continued improvement.
- Support CMC development including review and approval of QC specific documentation including CofAs, specifications, stability studies, method validation, test methods, process validation and all associated QC data.
- Support efforts to implement and utilize the internal electronic document management system.
- Support and review relevant sections of IND/IMPD/BLA
- Bachelor’s degree in a scientific discipline, post graduate degree is a plus.
- 7+ years of AD and or QC GMP experience in the Biotech/Pharmaceutical industry.
- Experience with CMOs, CMC development with focus on both large and small molecules.
- Experience of releasing or supporting release of clinical or commercial drug substance & drug product.
- Current and strong working knowledge of 21 CFR Parts 210-211 and 11; EU cGMP/GLPs; and ICH quality and development guidelines.
- Current and strong working knowledge of OOS Investigations.
- Driven, results-oriented self-starter and excellent team player.
- Creative and pragmatic approach to problem solving and issue resolution.
- Able to travel domestically and internationally.
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.
Applicant Privacy Policy
https://www.denalitherapeutics.com/denali-applicant-privacy-policy
-
Seniority level
Not Applicable -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Biotechnology Research
Referrals increase your chances of interviewing at Denali Therapeutics by 2x
See who you knowGet notified about new Director of Quality Control jobs in South San Francisco, CA.
Sign in to create job alertSimilar Searches
Looking for a job?
Visit the Career Advice Hub to see tips on interviewing and resume writing.
View Career Advice Hub