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Associate Manufacturing Engineer; Mon - Thur

Job in Salt Lake City, Salt Lake County, Utah, 84193, USA
Listing for: Denali Therapeutics
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Associate Manufacturing Engineer (Mon - Thur)

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.

The Associate Manufacturing Engineer’s responsibilities span from across Upstream/Downstream Unit Operations for both support and execution of manufacturing activities.

Key Accountabilities/Core

Job Responsibilities
  • Schedule Monday through Thursday with ability to alter schedule based on critical unit operation needs.
  • Responsibilities span across upstream and downstream for production campaigns and provide oversight of critical unit operations as area subject matter expert and provide continuous process sustainment activities to ensure process are in a state of control.
  • Coordinating with stakeholders to align activities to enable execution of production schedule (i.e. release of batch records, ensure Bill of Material (BOM) accuracy, etc.)
  • Ability to perform complex problem solving for both process and equipment related issues. Work with vendors when needed to bring equipment back into GMP state when issues arise.
  • Initiate Deviations and partner with Quality and other departments for investigations, impact assessment, determine root cause and execute preventive and corrective actions.
  • Collaborate with Process Engineering and MSAT for asset induction and develop subject matter expertise for ability to carry on sustainment responsibilities for the asset in question.
  • Lead implementation for process improvements and procedural updates.
  • Partner with MSAT on satellite and GLP processes in MSAT lab where applicable.
  • Review completed batch records and coordinate with QA for record closure.
  • Scheduling activities for routine maintenance required on assets based on availability and timing for CAL/PM due dates.
  • Conduct all activities in accordance with company policies & Standard Operating Procedures, global regulatory guidelines, environmental guidelines, as appropriate, etc.
  • Remain up to date on all assigned training and ensure completion of any training required for GMP activities prior to executing those activities
Qualifications/Skills
  • Bachelor’s degree in a Chemical, Mechanical or Biomedical Engineering or related relevant scientific or technical discipline with 1–2 years of applicable industry experience preferred. An advanced degree (MS or higher) in a related field may substitute for some or all the required experience. Relevant disciplines include, but are not limited to, Biology, Biochemistry, Chemistry, Biotechnology, or related life sciences.
  • Builds trustful and effective relationships with authenticity and humility.
  • Confidence to work in a rapidly changing environment.
  • The ability to contribute to a team where employees have a shared purpose and vision; foster a “One Denali” environment.
  • Strong self-awareness of the impact communication and working style has on others.
  • Proficient verbal and written communication skills.
  • Physical – must be able to put on specialized gowning, lift and manipulate items over 25 lbs, climb ladders, stand for multiple hours at a time.
  • Must be able to wear personal protective equipment (e.g., safety shoes, gloves, eye covering, etc.) in a compliant manner for extended periods of time.
Preferred Qualifications
  • Previous bio-manufacturing experience in a regulated industry.
  • Experience in product/process support within a regulated setting.
  • Experience with Good Documentation Practices and Good Manufacturing Practices.

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.

Salt

Lake City Drug Testing Policy#J-18808-Ljbffr
Position Requirements
10+ Years work experience
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