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Full Time Master Software Engineer Jobs in Bend, OR

Develops and executes protocols for equipment IQ/OQ/PQ in alignment with site validation master ... software and systems Education and Experience * Bachelor's degree in relevant technical field

SCADA Support Engineer

Bend, OR · On-site

$86K - $107K/yr

This role is based full-time in our office in San Diego, CA or Bend, OR. Specific location details ... Utilize software based diagnostic tools to aid in troubleshooting of complex plant SCADA systems.

SCADA Support Engineer

Bend, OR · On-site +1

$86K - $107K/yr

This role is based full-time in our office in San Diego, CA or Bend, OR. Specific location details ... Utilize software based diagnostic tools to aid in troubleshooting of complex plant SCADA systems.

Proficient in modeling structural systems using Revit BIM software with guidance from engineers or ... Applicants must be currently authorized to work in the United States on a full-time basis. Cushing ...

CNC Machinist

Redmond, OR · On-site

$65K - $80K/yr

Job Type Full-time Description Company Overview Integrated 3D™ LLC (i3D MFG™) is the premier a ... CAM software (e.g., Mastercam, SolidCAM) and G-code programming. • Knowledge of machining ...

... developers and builders and researches local zoning plans, master planning reports, and other ... Regular full-time employees are offered medical, dental, vision, and life insurance options. We ...

New

... developers and builders and researches local zoning plans, master planning reports, and other ... Regular full-time employees are offered medical, dental, vision, and life insurance options. We ...

New

Serve as the technical super-user for modern supply chain planning software, unlocking advanced ... Engineering, Operations Research, or a highly quantitative field. * A Master's degree or ...

Serve as the technical super-user for modern supply chain planning software, unlocking advanced ... Engineering, Operations Research, or a highly quantitative field. * A Master's degree or ...

... Master's-level professionals to join our Oregon Clinical Cohort . This is a full-time (W-2) , fully ... Charlie Health will never ask you to pay a fee or download software as part of the interview ...

Project Manager

Redmond, OR · On-site

$120K - $160K/yr

Marcum & Sons is currently seeking a full-time Project Manager to join our team. Marcum & Sons is a ... Technical expertise in civil engineering and construction practices, along with knowledge of ...

QC Testing Technician I

Redmond, OR · On-site

$19.75 - $25.50/hr

* Perform electrical and software tests on large HVAC equipment while working with exposed voltages ... Provide support to engineering staff as needed * Participate in maintaining a clean and safe work ...

QC Testing Technician I

Redmond, OR · On-site

$19.75 - $25.50/hr

* Perform electrical and software tests on large HVAC equipment while working with exposed voltages ... Provide support to engineering staff as needed * Participate in maintaining a clean and safe work ...

QC Testing Technician I

Redmond, OR · On-site

$19.75 - $25.50/hr

* Perform electrical and software tests on large HVAC equipment while working with exposed voltages ... Provide support to engineering staff as needed * Participate in maintaining a clean and safe work ...

Showing results 21-40

Full Time Master Software Engineer information

See Bend, OR salary details

$67K

$155.6K

$216.8K

How much do full time master software engineer jobs pay per year?

As of Aug 11, 2026, the average yearly pay for full time master software engineer in Bend, OR is $155,637.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,600.00 and $182,500.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Master Software Engineer vs Senior Software Engineer?

AspectFull Time Master Software EngineerSenior Software Engineer
QualificationsBachelor's or higher in CS or related field, advanced coding skillsBachelor's or higher, extensive coding experience
Work EnvironmentTeam-based, collaborative projects in tech companiesSame as Master Software Engineer, often leading projects
ResponsibilitiesDesign, develop, and maintain software solutionsLead development efforts, mentor juniors, oversee project modules
Usage in IndustryCommonly listed in job postings for experienced developersOften a step before managerial roles, recognized for expertise

Both roles require strong technical skills and similar educational backgrounds. The Master Software Engineer typically focuses on technical development, while the Senior Software Engineer may have additional leadership responsibilities. The main difference lies in scope of leadership and project oversight.

What are popular job titles related to Full Time Master Software Engineer jobs in Bend, OR? For Full Time Master Software Engineer jobs in Bend, OR, the most frequently searched job titles are:
What cities near Bend, OR are hiring for Full Time Master Software Engineer jobs? Cities near Bend, OR with the most Full Time Master Software Engineer job openings:
Infographic showing various Full Time Master Software Engineer job openings in Bend, OR as of August 2026, with employment types broken down into 1% Internship, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $155,637 per year, or $74.8 per hour.

Senior Validation Engineer

Serán BioScience

Bend, OR • On-site

Full-time

PTO

Re-posted 2 days 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.