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Biotech Software Engineer Jobs in Oregon (NOW HIRING)

Serán BioScience

Senior Validation Engineer

Bend, OR · On-site

... software and systems Education and Experience * Bachelor's degree in relevant technical field ... biotech industry * 8 years of GMP compliance experience, including knowledge of 21 CFR Part 11 ...

Seran BioScience

Senior Validation Engineer

Bend, OR

... software and systems Education and Experience * Bachelor's degree in relevant technical field ... biotech industry * 8 years of GMP compliance experience, including knowledge of 21 CFR Part 11 ...

Revvity

OR · On-site

Encourage customers to purchase training, support, software, laboratory services products and field ... Bachelor's Degree in Life Sciences, Electronics, Mechanics, Biotechnology or related discipline and ...

RAND Corporation

Associate AI Security Resident

OR · On-site +1

... intelligence and biotechnology-to shape policies that protect global security and advance the ... Required: * Technical experience in security engineering, software engineering, firmware ...

Revvity

Field Service Engineer

Salem, OR · On-site

Encourage customers to purchase training, support, software, laboratory services products and field ... Bachelors Degree in Life Sciences, Electronics, Mechanics, Biotechnology or related discipline and ...

e184

Head of Bioengineering

Portland, OR · On-site

About us e184 Artificial Womb is a biotechnology research company dedicated to advancing next ... engineering teams across mechanical, electrical, software, and computational domains while ...

e184

Head of Bioengineering

Portland, OR

About us e184 Artificial Womb is a biotechnology research company dedicated to advancing next ... engineering teams across mechanical, electrical, software, and computational domains while ...

Nvidia

OR · On-site

Our Solutions Architects are elite developers, scientists, and technical leaders who thrive at the ... Build proof-of-concept demonstrations that show how NVIDIA software and hardware accelerate ...

Nvidia

OR · On-site

Work with product, solution architecture, developer relations, and ISV teams to shape healthcare ... Engage cloud service providers, global system integrators, software partners, and channel teams to ...

Nvidia

OR · On-site

As a pioneer in accelerated computing, NVIDIA empowers pharmaceutical, biotech, and healthcare ... In this role, you will partner with leading pharmaceutical companies, techbios, and software ...

RAND Corporation

OR · On-site

... biotechnology-to shape policies that protect global security and advance the public good ... In this senior leadership role, you will oversee a large research and engineering portfolio focused ...

Koerber

Account Manager

OR · Remote

You will collaborate with Sales Engineers and Product teams to deliver value-based solutions ... biotech manufacturing industry. Our first in class Werum PAS-X software offering allows our ...

Körber Group

Account Manager

OR · On-site +1

You will collaborate with Sales Engineers and Product teams to deliver value-based solutions ... biotech manufacturing industry. Our first in class Werum PAS-X software offering allows our ...

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All JobsBiotech Software Engineer JobsBiotech Software Engineer Jobs in Oregon

Biotech Software Engineer information

See Oregon salary details

$67.1K

$156K

$217.3K

How much do biotech software engineer jobs pay per year?

As of Jun 10, 2026, the average yearly pay for biotech software engineer in Oregon is $155,975.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,900.00 and $182,900.00 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 Oregon? The most popular types of Biotech Software Engineer jobs in Oregon are:
What are popular job titles related to Biotech Software Engineer jobs in Oregon? For Biotech Software Engineer jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Biotech Software Engineer jobs in Oregon look for? The top searched job categories for Biotech Software Engineer jobs in Oregon are:
What cities in Oregon are hiring for Biotech Software Engineer jobs? Cities in Oregon with the most Biotech Software Engineer job openings:
Biotech Software Engineer jobs near you
Infographic showing various Biotech Software Engineer job openings in Oregon as of June 2026, with employment types broken down into 68% Full Time, 16% Part Time, 12% Contract, and 4% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $155,975 per year, or $75 per hour.

Senior Validation Engineer

Serán BioScience

Bend, OR • On-site

Full-time

PTO

Posted 11 hours ago

Job description

Serán BioScience is motivated to find an industry-experienced Validation Engineer to support the development of a new commercial manufacturing facility. The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer of manufacturing process from clinical to commercial site, and subsequent validation for process, cleaning, and computerized systems to support commercial distribution of non-sterile pharmaceutical products. Experience will determine title and salary, with preference given to applicants with over 8 years of experience with Oral Solid Dosage and an interest in leading teams. Those with less experience are encouraged to apply.
As a critical member of the Commercial Steering Committee, the Senior Validation Engineer will be responsible for planning and execution of CQ and validation projects. In order to perform this task, applicants require a thorough understanding of the manufacturing processes and systems as well as an understanding of all applicable regulations, guidelines, policies, procedures, and requirements. Successful candidates will understand that the development and execution of CQ and validation projects requires communication with internal and external cross functional teams. Demonstrated ability with effective communication is essential for identifying required information, alignment of strategies, and mitigation risks while maintaining good working relationships.
Duties and Responsibilities
  • Leads the commissioning and qualification (C&Q) of new and existing equipment and systems for OSD manufacturing, facilities, and utilities, ensuring compliance with cGMP, FDA, and EU regulatory standards
  • Supports the clinical technology transfer and operations in design, scale-up, optimization, and troubleshooting of OSD processes and equipment
  • Develops and executes protocols for equipment IQ/OQ/PQ in alignment with site validation master plans and project timelines
  • Collaborates with cross-functional teams to define equipment specifications, user requirements (URS), and establish project timelines and budgets
  • Manages installation activities, equipment FAT/SAT execution, and vendor coordination to ensure technical and compliance requirements are met
  • Collaborates with multidisciplinary team to complete change controls, deviations investigations, and CAPAs as required
  • Supports regulatory inspections and client audits
  • Performs other related duties as assigned
  • Responsibilities may increase in scope to align with company initiatives

Required Skills and Abilities
  • Demonstrates knowledge of cGMPs guidelines and regulations acquired through education, experience, and training
  • Preference for those who posses knowledge of Global Regulatory requirements (E.g., FDA / MHRA / EMEA)
  • Showcases foundational understanding of the compliance and technical requirements for the application of various scientific concepts used in developing different dosage forms of pharmaceutical products (primarily oral solid dose, while experience with sterile products is desired)
  • Experience with regulatory expectations and industry practices for CQ and Validation using Product Lifecycle approach
  • Experience with designing CQV plans for Facilities, Utilities, and Process equipment desired
  • Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team
  • Strong time-management skills and the ability to organize and coordinate multiple projects at once
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
  • Ability to prioritize tasks and to keep leadership apprised of performance timelines
  • Accepts feedback from a variety of sources and constructively manages conflict
  • Demonstrates leadership skills with ability to motivate and coach cross functional teams
  • Experience in FAT/SAT of process equipment, and knowledge operating principles of typical OSD process equipment preferred.
  • Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with aptitude to learn new software and systems

Education and Experience
  • Bachelor's degree in relevant technical field
  • Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing
  • Fundamental understanding of process equipment, utilities, manufacturing process, cleaning process and Quality systems used in the pharmaceutical/biotech industry
  • 8 years of GMP compliance experience, including knowledge of 21 CFR Part 11 requirements, GAMP 5, among others

Physical Requirements
  • Prolonged periods of sitting or standing at a desk and working on a computer
  • Prolonged periods of sitting or standing in a manufacturing environment
  • Must be able to lift fifteen pounds at times
  • Adheres to consistent and predictable in-person attendance

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
Level and compensation will be based on experience.
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Benefits Summary:
Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance.
The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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