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Preclinical Research Engineer Jobs (NOW HIRING)

Several years building and deploying AI/ML systems, ideally within preclinical research or drug discovery. Agentic Engineering Proven experience designing and deploying complex agentic AI systems in ...

... preclinical research or drug discovery. Agentic Engineering • Proven experience designing and deploying complex agentic AI systems in production environments. • Strong expertise in LLMs, agent ...

Drive innovation and evidence generation by partnering with R&D, preclinical, engineering, translational medicine and commercial stakeholders to design, evaluate and interpret studies, select ...

Senior Scientist, Human Milk Research

Evansville, IN · On-site

$93K - $119K/yr

... Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner ... Mead Johnson Nutrition is seeking a Senior Scientist to join its Human Milk Preclinical Research ...

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Preclinical Research Engineer information

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$37K

$106K

$142.5K

How much do preclinical research engineer jobs pay per year?

As of Jul 20, 2026, the average yearly pay for preclinical research engineer in the United States is $106,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $104,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Preclinical Research Engineer, and why are they important?

To thrive as a Preclinical Research Engineer, you need a solid background in biomedical engineering, biology, or a related field, along with experience in experimental design and data analysis. Familiarity with laboratory instrumentation, imaging systems, Good Laboratory Practice (GLP) standards, and relevant software such as MATLAB or statistical tools is crucial. Strong problem-solving abilities, attention to detail, and effective collaboration skills help set exceptional candidates apart. These competencies are vital for ensuring high-quality research outcomes, regulatory compliance, and successful cross-disciplinary teamwork in the preclinical development process.

What are preclinical research engineers?

Preclinical research engineers are professionals who design, develop, and test medical devices, pharmaceuticals, or other health-related products in the preclinical stage before they are used in human trials. They work with scientists and medical experts to ensure products meet safety and regulatory standards by conducting laboratory research, animal studies, and data analysis. Their work is crucial in identifying potential issues early and ensuring that only the safest and most effective products move forward to clinical trials.

What are some common challenges faced by Preclinical Research Engineers when transitioning new devices from concept to animal studies?

Preclinical Research Engineers often encounter challenges related to regulatory compliance, experimental design, and cross-functional collaboration when moving new devices from the conceptual phase to animal testing. Ensuring that prototypes meet safety and ethical standards while generating reliable, reproducible data can be complex and requires meticulous planning. Additionally, close coordination with biologists, veterinarians, and regulatory experts is essential to address issues such as animal welfare, data integrity, and timely project milestones. Being proactive in communication and documentation helps navigate these challenges and supports successful project advancement.

What is the difference between Preclinical Research Engineer vs Laboratory Technician?

AspectPreclinical Research EngineerLaboratory Technician
Required CredentialsBachelor's or Master's in Biomedical, Biological, or related fields; some roles may require certifications in lab techniquesAssociate's or Bachelor's degree; technical training or certifications often preferred
Work EnvironmentResearch labs, pharmaceutical companies, biotech firms, often involved in experimental design and data analysisLaboratories performing routine testing, sample preparation, and data recording
Employer & Industry UsageUsed in biotech, pharmaceutical, and research institutions focusing on preclinical studiesCommon in hospitals, research labs, and manufacturing settings for routine lab work

Preclinical Research Engineers focus on designing and conducting experiments to evaluate new drugs or therapies before clinical trials, requiring advanced education and analytical skills. Laboratory Technicians perform routine lab tasks, supporting research activities with less emphasis on experimental design. Both roles are essential in the research process but differ in responsibilities and qualifications.

More about Preclinical Research Engineer jobs
What cities are hiring for Preclinical Research Engineer jobs? Cities with the most Preclinical Research Engineer job openings:
What states have the most Preclinical Research Engineer jobs? States with the most job openings for Preclinical Research Engineer jobs include:
Infographic showing various Preclinical Research Engineer job openings in the United States as of July 2026, with employment types broken down into 70% Full Time, 10% Temporary, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $106,012 per year, or $51 per hour.
Staff Scientist, Pharmaceutical Development

Staff Scientist, Pharmaceutical Development

Septerna

South San Francisco, CA

$160K - $180K/yr

Other

Re-posted 8 days ago


Job description

THE ROLE

We are seeking an experienced Staff Scientist with expertise in formulation development to support our small molecule pipeline. They will ensure that fit for purpose formulations are used for nonclinical in vivo studies. They will design, execute, manage, and analyze studies to develop and deliver formulations that support nonclinical DMPK, pharmacology, and toxicology studies. They may also support the development of clinical formulations.

This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams.

Responsibilities

  • Develop early formulation strategies and serve as an SME to deliver fit-for-purpose formulations supporting PK, PD, efficacy, and safety preclinical studies through discovery to candidate selection across research programs.
  • Design, manage, and execute early formulation screening studies to enable high-quality in vivo data, including solubility assessments, excipient compatibility, enabling approaches, and stability.
  • Implement early formulation development and preparation workflows, tools, templates, and best practices internally and in partnership with CDMOs/CROs to support preclinical studies.
  • Represent early formulation on cross-functional research teams, presenting data and recommendations to ensure aligned and timely support.
  • Author and review technical documents to support early formulation activities and preclinical studies, including development reports and study protocols.
  • Manage multiple priorities in a fast-paced, dynamic environment and enact quick problem solving to ensure on-time supply of formulations to support preclinical studies across programs.

Qualifications

  • A PhD, MS, or BS in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or a related field with a minimum of 6 years, 10 years, or 12 years, respectively, of relevant industry experience in small molecule formulation development.
  • Demonstrated success delivering formulation strategies to support preclinical research studies using data-driven, riskbased strategies.
  • Experience in small molecule formulation development across multiple routes of administration, including powders, solid dosage forms, solutions, suspensions, nanoparticles, and lipidbased systems.
  • Hands-on experience with analytical techniques to support small molecule formulation development, including UPLC/HPLC and solid-state characterization techniques (e.g., particle size analysis, DSC, DVS, PLM, and XRPD).
  • Working knowledge and practical application of current industry and compendial standards and regulatory authority guidance and expectations, including ICH, FDA, MHRA, and EMA guidelines and USP-NF, Ph. Eur, BP, and JP compendia.
  • Ability to manage and collaborate with external partners, including consultants and CDMOs/CROs.
  • Excellent interpersonal and communication skills (written and oral) with the ability to effectively prepare high-quality technical documentation and concisely present data to peers, management, and external groups.
  • Exhibited strong organizational and critical thinking skills with an attention to detail and data integrity enabling sound, technically driven decision making.
  • Able to travel domestically and internationally as needed, up to 20% of the time.

The anticipated salary range for candidates who will work in South San Francisco, CA is $160,000 - $180,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.

We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. 

Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.