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Pharmaceutical Validation Engineer Jobs in Oregon

Telix Pharmaceuticals (AMER)

Sustainability Engineer

OR · On-site +1

$91K - $112K/yr

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

Serán BioScience

Process Engineer

Bend, OR

Partner with Validation, QA, and Manufacturing to ensure compliance with regulatory requirements ... in pharmaceutical manufacturing, process engineering, or industrial engineering * Hands-on ...

Serán BioScience

Process Engineer

Bend, OR · On-site

Partner with Validation, QA, and Manufacturing to ensure compliance with regulatory requirements ... in pharmaceutical manufacturing, process engineering, or industrial engineering * Hands-on ...

Seran BioScience

Process Engineer

Bend, OR · On-site

Partner with Validation, QA, and Manufacturing to ensure compliance with regulatory requirements ... in pharmaceutical manufacturing, process engineering, or industrial engineering * Hands-on ...

Serán BioScience

Senior Engineer, Process Development

Bend, OR · On-site

$109K - $141K/yr

... pharmaceutical drug products from early clinical manufactures through late-stage process validation ... The Senior Engineer will collaborate with experts in formulation and product design and analytical ...

Seran BioScience

Senior Engineer, Process Development

Bend, OR · On-site

$109K - $141K/yr

... pharmaceutical drug products from early clinical manufactures through late-stage process validation ... The Senior Engineer will collaborate with experts in formulation and product design and analytical ...

Serán BioScience

Senior Engineer, Process Development

Bend, OR · On-site

$109K - $141K/yr

... pharmaceutical drug products from early clinical manufactures through late-stage process validation ... The Senior Engineer will collaborate with experts in formulation and product design and analytical ...

Seran BioScience

Quality Assurance Engineer

Bend, OR · On-site

Supports validation lifecycle activities such as, but not limited to, change management, periodic ... Minimum of 4 years required within pharmaceutical industry, with preference given to those with 5 ...

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Showing results 21-40

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 Sep 4, 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 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 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 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 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 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 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $114,348 per year, or $55 per hour.

Senior Quality Assurance Engineer

Genentech, Inc.

Hillsboro, OR • On-site

$93K - $172K/yr

Full-time

Re-posted 26 days ago

Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

This role is a valuable part of our Hillsboro Innovative Therapies (HIT) Quality Systems and Validation team, which is committed to achieving our mission of delivering novel and exciting biopharmaceutical technologies to patients. As a member of this dedicated cross-functional team, you will drive production start-up activities and establish the foundational quality approach for new facilities. You will have the opportunity to collaborate closely with key stakeholders in Engineering, Operations, and global network teams to ensure our systems and processes are safe, compliant, and inspection-ready.
The Opportunity
As a Senior Quality Assurance Engineer, you will provide day-to-day Quality Oversight for site qualification, equipment validation, and computer system validation during critical production start-up activities. You will act as the site Quality and Regulatory Subject Matter Expert (SME), ensuring that all local processes and automated systems strictly align with current Good Manufacturing Practices (cGMPs). Key responsibilities include:
  • Lead Quality Oversight: Provide technical and regulatory oversight for site qualification and validation activities, including advanced Computer System Validation (CSV).
  • Approve Critical Validation: Review and approve essential lifecycle documentation such as Validation Master Plans, User Requirements, Protocols, deviations, and Summary Reports.
  • Support Engineering & Design: Collaborate during the build and deploy phases to support user requirement definitions and design specifications for production and laboratory equipment.
  • Defend Inspection Readiness: Maintain the compliance status of assigned areas to ensure a constant state of inspection readiness, and directly present and defend the validation program during regulatory audits.
  • Manage Risk & Changes: Provide technical quality assessments and approvals for engineering modifications, process changes, and Corrective and Preventive Actions (CAPAs) while managing the validation risk log.
  • Drive Continuous Improvement: Partner with interdepartmental, multi-site, and global corporate teams to implement validation best practices and benchmark against industry standards.

Who You Are
  • Education & Experience: Bachelor's degree (preferably in Engineering or Life Sciences) with a minimum of 8 years of pharmaceutical/biopharmaceutical industry experience, or a Master's degree with a minimum of 6 years of relevant industry experience. Cell therapy experience is preferred.
  • Validation & Engineering Expertise: Possess sound knowledge of engineering principles, qualification concepts, and regulatory requirements as they relate to system performance and laboratory design/start-up activities.
  • Automation & Systems Knowledge:Technical familiarity with the design, build, and deployment of automation and execution systems (such as Delta V/SCADA, Syncade MES, BAS, EBR, and Pi Data historian) within a regulated environment.
  • Regulatory & Risk Frameworks: Strong understanding of US and EU cGMPs, validation guidelines, and Risk Assessment Methodologies (such as PHA, FMEA, and FTA).
  • Decision-Making & Quality Analysis: Demonstrated ability to interpret complex Quality standards, make sound technical decisions, and troubleshoot cross-functional quality issues effectively.
  • Collaborative Communication: Excellent verbal and written communication skills with a proven track record of working collaboratively in cross-functional teams to achieve project milestones.
  • Physical & Travel Requirements:Ability to meet standard office physical demands (sitting/standing for extended periods, lifting up to 25 lbs) and a willingness to travel up to 30% to other sites as required.

The expected salary range for this position based on the primary location of Oregon is $93,000 - $172,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this link.
This is an on-site position.
Relocation benefits are approved for this posting.
#LI-CA1
#ptcareers
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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