This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.This position is responsible for characterizing/validating purification processes and authoring IND/BLA sections to support our large molecule pipeline.Key Accountabilities/ Core Job Responsibilities:
Lead purification/downstream process characterization, tech transfer, and late-stage activities
Author protocols, coordinate study execution, review analytical results, generate/review reports, and author IND/BLA sections
Coordinate internal team to generate late-stage process characterization and/or validation data packages
Support selection/coordination of CDMOs as needed to generate high-quality late-stage data packages
Transfer purification processes to CMOs and support ongoing manufacturing activities as needed
Support other late-stage projects and apply lessons learned to current projects
Design and execute lab-scale chromatography and filtration studies to inform and support large scale process decisions
Maintain existing workflows to provide purification support for cell line and cell culture development activities
Execute methods for in-process testing using ELISA, HPLC, UV and SDS-Page based analytics
Qualifications/Skills:
PhD in Biology, Biochemistry, Chemical Engineering or related scientific discipline plus a minimum of 5+ years of purification development experience in the biotech/biopharma industry.
Experience with purification process characterization and validation is required.
Experience reviewing batch records and familiarity with Process Performance Qualification (PPQ) campaigns.
Familiarity with BLA authoring is preferred.
Proven track record of representing bioprocess functions in cross-functional teams and working effectively with CMOs.
Broad experience in process characterization, design of experiments and analytics.
Experience developing protein purification processes to support early or late-stage clinical production.
Knowledge of process virology, including working with contract labs to plan and execute viral clearance studies, is desired.
Expertise in AKTA protein purification systems and antibody characterization methods including: HPLC, LC/MS, SDS‐PAGE, DLS and other biophysical techniques.
Excellent critical thinking, scientific problem-solving and communication skills.
Compensation and Benefits:
Salary Range: $147,000.00 to $191,000.00 .
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience.
Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits.
Learn more at
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.
“Life at Denali” is a living reflection of our values: trust, unity, grit and growth. These are not just words we share—they shape how we show up, collaborate and push boundaries together. From the lab to the community, across functions and milestones, our culture thrives on shared purpose and relentless pursuit.
#J-18808-Ljbffr
Worksite address
south san francisco, CA, 94083, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.