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Pharmaceutical Validation Engineer Jobs in Oregon

Serán BioScience

Senior Validation Engineer

Bend, OR · On-site

The Senior Validation Engineer will be part of a cross functional team that will plan and execute ... pharmaceutical products. Experience will determine title and salary, with preference given to ...

CAI

Validation Engineer

Portland, OR · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... the Pharmaceutical/Life Sciences industry - Essential experience in a GMP (Good Manufacturing ...

CAI

Validation Engineer

Portland, OR

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... the Pharmaceutical/Life Sciences industry - Essential experience in a GMP (Good Manufacturing ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Technical Experience * 7-11 years of experience in the biotech, pharmaceutical, or medical device ...

CAI

Validation Engineer

Portland, OR · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... the Pharmaceutical/Life Sciences industry - Essential experience in a GMP (Good Manufacturing ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Technical Experience * 7-11 years of experience in the biotech, pharmaceutical, or medical device ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Technical Experience * 7-11 years of experience in the biotech, pharmaceutical, or medical device ...

Stark Pharma Solutions Inc

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

The ideal candidate will have extensive experience in pharmaceutical process design, OSD ... Collaborate with Engineering, Manufacturing, Quality, Validation, and external vendors to ensure ...

Arcus Biosciences

... Engineering, or a similar discipline (or equivalent experience). • 10+ years of experience in computer system validation activities in the pharmaceutical, biotechnology, or related industry ...

Telix Pharmaceuticals (AMER)

OR

$91K - $112K/yr

... validation activities, CDMO (Contract Development/Manufacturing Organization) qualification ... pharmaceutical or biopharmaceutical industry, including GMP. PET manufacturing, handling of ...

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All JobsPharmaceutical Validation Engineer JobsPharmaceutical Validation Engineer Jobs in Oregon

Pharmaceutical Validation Engineer information

See Oregon salary details

$23

$54

$82

How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for pharmaceutical validation engineer in Oregon is $54.98, according to ZipRecruiter salary data. Most workers in this role earn between $41.68 and $66.83 per hour, depending on experience, location, and employer.

What is the difference between Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation engineer?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What does a pharmaceutical validation engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the most common challenges a pharmaceutical validation engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.

What are popular job titles related to Pharmaceutical Validation Engineer jobs in Oregon?

For Pharmaceutical Validation Engineer jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Validation Engineer jobs in Oregon look for?

The top searched job categories for Pharmaceutical Validation Engineer jobs in Oregon are:

Pharmaceutical Validation Engineer jobs near you
Infographic showing various Pharmaceutical Validation Engineer job openings in Oregon as of August 2026, with employment types broken down into 87% Full Time, 6% Part Time, 6% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $114,348 per year, or $55 per hour.

Senior Validation Engineer

Seran BioScience

Bend, OR

Full-time

PTO

Re-posted 4 days ago

Job description

Seran 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:
Seran 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. Seran 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 Seran 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.
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