Maze Therapeutics

Scientist I, Bioanalytical

Maze Therapeutics$130K — $159K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in analytical chemistry, chemistry, biochemistry, or related field.
  • 6+ years of relevant experience in bioanalysis oversight, ideally within a pharmaceutical company, CRO, or academia.
  • Understanding and experience with GLP and GCLP principles and guidances.
  • Proficient in bioanalytical techniques, including LC-MS/MS, ELISA, and MSD.
  • Proven track record of working within multidisciplinary project teams.
  • Strong ability to handle multiple projects with attention to detail.
  • Effective communication skills for presenting scientific information.

Responsibilities

  • Oversee the development, validation, and execution of bioanalytical assays for pharmacokinetics and pharmacodynamics.
  • Manage collaborations with contractor laboratories for bioanalysis and review results for accuracy.
  • Provide written summaries of bioanalytical methods for regulatory submissions as needed.
  • Coordinate regulated bioanalysis activities across development programs to meet compliance standards.
  • Update timelines for bioanalysis activities and collaborate with stakeholders to address project issues.
  • Investigate and coordinate resolution of data integrity queries with CRO personnel.

Benefits

  • Competitive medical, dental, and vision insurance.
  • Mental health offerings and resources.
  • Equity incentive plan to enhance employee ownership.
  • 401(k) program with employer match.
  • Generous holiday and PTO policy.
Full Job Description
The Position

We are seeking a detail-oriented Scientist to work in the Non-Clinical Development department overseeing bioanalytical work for Maze. In this role, you will oversee bioanalysis for Good Laboratory Practices (GLP), Good Clinical Laboratory Practices (GCLP), and non-GLP studies in support of the development of small molecule drugs. As part of the Non-Clinical Development team, you will have the opportunity to contribute to key drug discovery and development projects.

This position reports to VP, Non-Clinical Development.
The Impact You'll Have
  • Oversee the development, validation, and execution of bioanalytical assays for both pharmacokinetics and pharmacodynamics for ongoing preclinical, nonclinical, and clinical programs.
  • Manage the collaborations with contractor laboratories conducting bioanalysis and review data from analysis to confirm analyses were correctly conducted and batch analyses met acceptance criteria.
  • Provide written summaries of bioanalytical methods for regulatory submissions as needed.
  • Coordinate regulated bioanalysis activities across development programs, ensuring compliance with timelines and regulatory standards.
  • Provide timeline updates to the Head of Bioanalysis, Nonclinical Development, and collaborate with key stakeholders in Research, Regulatory Affairs, Manufacturing, Quality, and Clinical Sciences to address bioanalysis-related project issues.
  • Review, investigate, and coordinate resolution of study queries with contract research organization (CRO) and personnel regarding data integrity.
What We're Looking For
  • Bachelor's degree in analytical chemistry, chemistry, biochemistry, or related field.
  • 6+ years of relevant experience, ideally within a pharmaceutical company, a CRO, or academia, with a focus on bioanalysis oversight.
  • Experience and understanding of GLP and GCLP principles and guidances
  • Experience in GLP and GCLP analysis of one or more bioanalytical techniques, including: LC-MS/MS, ELISA, and MSD
  • Experience working with multidisciplinary project teams, driving successful outcomes.
  • Ability to manage multiple projects simultaneously with excellent attention to detail.
  • Clear and effective communication skills to present complex scientific information to various stakeholders.


The expected annual salary range for employees located in the San Francisco Bay Area is $130,000 - $159,000. Additionally, this position is eligible for an annual performance bonus.

Maze performs position-based compensation benchmarking to industry market data to ensure we pay competitive wages. Determination of starting salary will depend upon a variety of job-related factors, which may include professional experience, skills, and job location. The expected salary range for this role may be modified in the future.

Maze offers a robust benefits package to our eligible employees including competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with employer match and a generous holiday and PTO policy.

#LI-Hybrid

About Maze Therapeutics

Maze Therapeutics is a biotechnology company that is focused on developing precision therapies for genetically defined diseases. The company's approach is based on the use of genetic modifiers, which are small molecules that can modulate the expression of disease-causing genes. Maze Therapeutics is leveraging its proprietary platform to identify and develop genetic modifiers for a range of diseases, including cancer, neurological disorders, and rare genetic diseases. The company was founded in 2019 and is headquartered in Menlo Park, California.
Learn more about Maze Therapeutics
Industry
Founded
2019

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