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Biotech Software Engineer Jobs in Kansas (NOW HIRING)

... functions (engineering, exhibit batches, etc), as well as on-going stability studies. The ... Understanding of various scientific software or software used in pharmaceutical or production ...

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Biotech Software Engineer information

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$56.6K

$131.6K

$183.3K

How much do biotech software engineer jobs pay per year?

As of Jun 30, 2026, the average yearly pay for biotech software engineer in Kansas is $131,569.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $154,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biotech Software Engineer position, and why are they important?

To thrive as a Biotech Software Engineer, you need a solid background in computer science or software engineering, coupled with an understanding of biology, genetics, or related life sciences. Familiarity with programming languages such as Python or Java, experience using bioinformatics tools (like BLAST or Bioconductor), and, in some settings, knowledge of regulatory standards are highly valuable. Strong problem-solving abilities, effective communication, and the ability to work well in interdisciplinary teams distinguish top performers in this field. These skills are crucial for building reliable software solutions that support scientific discovery and innovation in biotechnology organizations.

What are some typical projects or daily tasks for a Biotech Software Engineer?

As a Biotech Software Engineer, you'll often develop and maintain software tools for analyzing biological data, automate laboratory workflows, or create user-friendly interfaces for scientific researchers. Your daily tasks might include writing code, troubleshooting algorithms, reviewing scientific data, and collaborating closely with biologists, data scientists, and laboratory technicians. Depending on the company, you may be involved in developing cloud-based platforms, integrating new laboratory hardware, or ensuring software compliance with industry regulations. This dynamic and collaborative environment means your work directly impacts ongoing research and helps accelerate scientific discoveries in the biotech sector.

What is a Biotech Software Engineer job?

A Biotech Software Engineer develops software solutions for the biotechnology industry, enabling research, data analysis, and automation in fields like genomics, bioinformatics, and drug discovery. They work with scientists to design algorithms, manage biological data, and create applications that support experiments and workflows. This role requires expertise in programming, cloud computing, and biological sciences to bridge the gap between technology and life sciences.

What are the most commonly searched types of Biotech Software Engineer jobs in Kansas? The most popular types of Biotech Software Engineer jobs in Kansas are:
What are popular job titles related to Biotech Software Engineer jobs in Kansas? For Biotech Software Engineer jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Biotech Software Engineer jobs in Kansas look for? The top searched job categories for Biotech Software Engineer jobs in Kansas are:
Infographic showing various Biotech Software Engineer job openings in Kansas as of June 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $131,569 per year, or $63.3 per hour.
Analytical Chemist

Analytical Chemist

Pioneer Data Systems

Mcpherson, KS • On-site

Contractor

Medical, Dental, Vision

Posted 27 days ago


Key responsibilities

  • Perform analytical testing using various equipment and wet chemistry methods in a GXP environment.

  • Enter and process experimental data in lab notebooks and LIMS systems, and review data entries from team members.

  • Author protocols, reports, and technical documents, and present project data to the group as needed.


Job description

Company Description
Job Description
Position Details:Job Title: Analytical Chemist I
Duration: 12 months contract, extendable up to 18 months
Location: Mcpherson, KS
Note:
Client has the right-to-hire you as a permanent employee at any time during or after the end of contract.
You may participate in the company group medical insurance plan which includes dental and vision.
Job Description:
The R&D Pharm Sci. team member will be involved in multiple, on-going projects. Activities include performing analysis in a GXP environment and may include material qualification (excipients or active pharmaceutical ingredients), release testing, and analysis required to support manufacturing functions (engineering, exhibit batches, etc), as well as on-going stability studies. The individual should have good communication and organizational skills and be able to coordinate work with cross-functional team members, peers, and external CROs (Contract Research Organization).
Position Responsibilities
Perform testing using analytical equipment (i.e. UPLC, HPLC, GC, Karl Fischer, pH, UV-Vis, IR, microscopy, optical rotation) as well as using traditional wet chemistry methods (i.e. titration, TLC, sulfated ash, etc.)
Enter experimental information into hard-bound and electronic lab notebooks (i.e. Biovia eLN) and process analytical data accordingly (i.e. Empower 3, Excel, etc).
Perform additional data entry, processing, and review within LIMS system (i.e. Thermo LIMS).
Coordinate with team members to ensure seamless analytical coverage during manufacturing campaigns and on-going stability studies. Also support new project activities, as needed.
Perform analytical method feasibility, development and validation, as necessary.
Coordinate with team members to verify each other's data by reviewing eLN and LIMS entries in a timely manner.
Take personal responsibility to meet analytical testing and data verification deadlines, as well as safety and training requirements.
Author protocols, reports, or other technical documents, and presents project data to group, as needed.
Organizational Relationships
Primary interaction will be with Pharmaceutical McPherson PEH PharmSci R&D group. Will also work with other product development groups including GTS and Pharmaceutical Center One.
Pharmaceutical McPherson Chemistry Quality group.
Pharmaceutical McPherson Manufacturing.
Possible interaction with CROs
Education And Experience
Indicate the formal education, certification or license(s) required and/or preferred. Include the minimum number of years of relevant experience required for the position (where legally permissible).
BS and 3-7 years experience in a regulated industry (i.e. food, pharmaceutical, biotech, petroleum, etc).
MS and 2-5 years experience in regulated industry
PhD and 1-5 experience in regulated industry
Technical Skills Requirements
Indicate the technical skills required and/or preferred, as applicable.
Hands-on experience with complex analytical equipment including IR, UV-Vis, imaging systems, chromatography systems (UPLC, HPLC, GC) and chromatography methods (RP, IC, SEC, etc).
Experience using simple analytical tools including KF titration, microscope, polarimeter, pH, analytical balances, density meter, osmometer, and etc. is required.
Experience with simple and/or complex analytical method verification, development, transfer, or validation strongly preferred.
Experience working in a regulated (i.e. FDA, TTB, etc) or GMP environment is strongly preferred.
Understanding of various scientific software or software used in pharmaceutical or production environment (i.e. eLN, LIMS, Empower 3, Trackwise, MiniTab, Fusion, etc) would be preferred.
Strong analytical reasoning skills.
Excellent written and verbal communication skills.
Physical Position Requirements
Note the physical conditions in which work will be performed, if applicable to the position. Examples: Lifting, sitting, standing, walking, ability to travel, drive, unusual attendance requirements, weekend work or travel requirements, etc. Please include any hazardous materials or non-standard working environment the contractor will have exposure to which may require additional medical testing and/or apparatus fitting for OSHA compliance.
May work with hazardous chemicals including acids, bases, oxidizing agents, carcinogens, mutagens, teratogens, etc.
Additional medical testing will be required.
PPE training, solvent respirator and powder respirator training and fitting will be required.
Occasional weekend and evening work is required.
May sit or stand at bench for extended periods.
Qualifications
Additional Information
Anuj Mehta
732-947-3452