1

Metrology Engineer Jobs in Washington (NOW HIRING)

Electrical Engineer Looking for an opportunity to make an impact? At Leidos , we deliver innovative ... Demonstrated experience using metrology equipment to test PCBs or system assemblies * Demonstrated ...

Electrical Engineer

Chantilly, VA · On-site

$131K - $237K/yr

Electrical Engineer Looking for an opportunity to make an impact? At Leidos , we deliver innovative ... Demonstrated experience using metrology equipment to test PCBs or system assemblies * Demonstrated ...

Quality Engineer II

Rockville, MD · On-site

$100K - $150K/yr

Who We're Looking For We are seeking a Quality Engineer II to support hardware build, integration ... Familiarity with metrology systems, calibration programs, and inspection tooling * Experience ...

Sr Engineer, Equipment

Manassas, VA · On-site

$104K - $143K/yr

Provide technical support to the manufacturing equipment repair and process engineering ... 3. Metrology tools including ASML Yield Star or KLA registration tools 4. Overlay analysis ...

Showing results 41-60

Metrology Engineer information

See Washington salary details

$29

$58

$89

How much do metrology engineer jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for metrology engineer in Washington is $58.15, according to ZipRecruiter salary data. Most workers in this role earn between $48.99 and $66.44 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a metrology engineer, and why are they important?

To thrive as a Metrology Engineer, you need a strong background in physics, mathematics, and engineering principles, typically supported by a bachelor's degree in engineering or a related field. Familiarity with measurement instruments, calibration systems, and software like MATLAB or LabVIEW is commonly required, with certifications such as ASQ Certified Calibration Technician considered beneficial. Attention to detail, analytical thinking, and effective communication skills help you excel in troubleshooting and collaborating with multidisciplinary teams. These competencies ensure precise measurement processes, maintain quality standards, and drive continuous improvement in manufacturing or laboratory environments.

What are some typical challenges metrology engineers face when integrating new measurement technologies into existing manufacturing processes?

Metrology Engineers often encounter challenges such as ensuring compatibility between new measurement tools and legacy equipment, maintaining calibration standards, and minimizing production downtime during implementation. They must also train staff on updated protocols and troubleshoot unexpected variances in measurement data. Successfully addressing these challenges requires strong problem-solving skills, meticulous attention to detail, and effective communication with cross-functional teams including production, quality, and maintenance departments.

What is a metrology engineer?

A metrology engineer, or metrologist, specializes in science or engineering-related measurements. Their duties may include calibrating instruments, designing new tools or systems of measurement, interpreting data, or researching the science of measuring. Many subfields work with metrologists, including mechanical engineering. There are two levels of metrology certification available through the Coordinate Metrology Society (CMS).

What does a metrology engineer do?

A Metrology Engineer specializes in the science of measurement, ensuring that instruments and processes produce precise and accurate results. Their responsibilities include calibrating measuring equipment, developing measurement methods, and analyzing data to support quality control and product development. They work across industries such as manufacturing, aerospace, and electronics to maintain standards and compliance. Metrology Engineers also contribute to troubleshooting measurement issues and improving measurement systems to enhance efficiency and reliability.

What is the difference between Metrology Engineer vs Quality Control Engineer?

AspectMetrology EngineerQuality Control Engineer
Required CredentialsBachelor's in Engineering, certifications in metrology or calibrationBachelor's in Engineering, certifications in quality assurance or control
Work EnvironmentLaboratories, calibration labs, manufacturing plantsManufacturing lines, inspection facilities, production environments
Employer & Industry UsageManufacturing, aerospace, automotive, electronicsManufacturing, consumer goods, pharmaceuticals, automotive
Common Search & Comparison IntentUnderstanding technical calibration roles, measurement accuracyEnsuring product quality, defect prevention

Metrology Engineers focus on precise measurement, calibration, and maintaining measurement systems, ensuring accuracy in manufacturing processes. Quality Control Engineers oversee product inspections and testing to ensure standards are met. While both roles aim to improve product quality, Metrology Engineers specialize in measurement systems, whereas Quality Control Engineers focus on final product quality assurance.

What are popular job titles related to Metrology Engineer jobs in Washington? For Metrology Engineer jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Metrology Engineer jobs in Washington look for? The top searched job categories for Metrology Engineer jobs in Washington are:
What cities in Washington are hiring for Metrology Engineer jobs? Cities in Washington with the most Metrology Engineer job openings:
What are popular job titles related to Metrology Engineer jobs in WA? For Metrology Engineer jobs in WA, the most frequently searched job titles are:
Infographic showing various Metrology Engineer job openings in Washington as of August 2026, with employment types broken down into 89% Full Time, and 11% Part Time. Highlights an 100% In-person job distribution, with an average salary of $120,961 per year, or $58.2 per hour.

Senior Small Molecule Manufacturing Subject Matter Expert

Tunnell Government Services

Bethesda, MD • On-site

$93K - $114K/yr

Full-time

Posted 16 days ago


Job description

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
Senior Small Molecule Manufacturing Subject Matter Expert (SME) with focus within either of these disciplines:
Small Molecule Validation/Scale-Up Engineering
Small Molecule Process/Product Development
Location: Remote (U.S.-based) with approximately 20-25% travel
Position Overview
The Senior Small Molecule Manufacturing SME will support the development and implementation of the Strategic Active Pharmaceutical Ingredients Reserve (SAPIR®) initiative under Executive Order 14336, a transformative effort aimed at strengthening U.S. pharmaceutical supply chain resiliency and ensuring uninterrupted access to critical generic medicines.
This role will help design and advance innovative approaches for domestic manufacturing of Active Pharmaceutical Ingredients (APIs) and finished drug products while supporting the creation of a strategic national reserve of critical active pharmaceutical ingredients. The initiative seeks to establish a resilient, agile, and distributed manufacturing ecosystem capable of rapidly converting API inventories into finished products during emergencies or supply disruptions.
The ideal candidate combines deep experience in traditional pharmaceutical manufacturing with a demonstrated ability to embrace emerging technologies and novel manufacturing paradigms. This individual will serve as a technical leader helping redefine how pharmaceutical products are developed, manufactured, stockpiled, and deployed in the United States.
Key Responsibilities
Strategic Manufacturing
  • Support development of a resilient domestic API manufacturing and stockpiling strategy for critical generic medicines.
  • Provide technical expertise to support large-scale reshoring of pharmaceutical manufacturing capabilities.
  • Develop innovative manufacturing approaches that reduce labor intensity, increase operational efficiency, and minimize facility footprint requirements.
  • Evaluate and implement scalable manufacturing models capable of supporting national preparedness and emergency response objectives.

Advanced Manufacturing & Technology Integration
  • Assess and implement emerging pharmaceutical manufacturing technologies, including:
    • Continuous flow chemistry
    • Continuous and modular manufacturing systems
    • Agile and distributed manufacturing models
    • Advanced process analytical technologies (PAT)
    • Real-time process monitoring and metrology
    • Engineered biological and enzymatic production systems
  • Identify opportunities to integrate automation, digital manufacturing, and advanced analytics into API and finished product manufacturing operations.
  • Collaborate with multidisciplinary teams to develop next-generation manufacturing solutions for small molecule drug products.

Data, Analytics & Regulatory Support
  • Leverage large manufacturing and process datasets to improve product quality, process understanding, and operational performance.
  • Assess applications of machine learning and advanced analytics within pharmaceutical manufacturing environments.
  • Support development of data-driven regulatory submissions and validation strategies.
  • Ensure manufacturing approaches align with applicable FDA and other regulatory requirements.

Manufacturing Operations & Scale-Up
  • Provide end-to-end expertise across API development, process development, manufacturing scale-up, commercial production, and supply chain operations.
  • Support design, startup, optimization, and operation of pharmaceutical manufacturing facilities and contract development and manufacturing organizations (CDMOs).
  • Identify opportunities to improve reliability, quality, and production efficiency throughout the manufacturing lifecycle.
  • Serve as a technical advisor on facility design, manufacturing strategy, and operational excellence initiatives.

Required Qualifications
  • Bachelor's degree required, Advanced degree strongly preferred in Chemical Engineering, Chemistry, Pharmaceutical Sciences, Biochemical Engineering, Electrical Engineering, Biology, or related technical discipline.
  • 15+ years of pharmaceutical manufacturing experience with significant expertise in small molecule drug substance and/or drug product manufacturing.
  • Experience in API stability assessment, shelf-life determination, and management of stored material requalification programs to ensure product quality, regulatory compliance, and uninterrupted supply.
  • Demonstrated expertise in Key Starting Material (KSM) and starting material sourcing strategy, including supply risk assessment, supplier evaluation, cost of goods (COGS) optimization, and make-versus-buy analysis to support manufacturing and supply chain decisions.
  • Proven experience building, operating, leading, or scaling pharmaceutical manufacturing facilities and/or CDMOs.
  • Deep understanding of pharmaceutical manufacturing processes, technology transfer, process development, and commercial operations.
  • Strong knowledge of FDA-regulated manufacturing environments, including GMP requirements and regulatory expectations.
  • Demonstrated ability to work across multiple functional areas and solve complex technical and operational challenges.
  • Ability to evaluate emerging technologies and implement innovative manufacturing solutions.

Preferred Qualifications
  • Experience with:
    • Continuous flow chemistry
    • Continuous manufacturing
    • Modular manufacturing systems
    • Process Analytical Technology (PAT)
    • Advanced process controls
    • Machine learning and manufacturing analytics
    • Pharmaceutical process development
    • Analytical chemistry
    • Chemistry development and scale-up
    • Enzyme-based or engineered biological production platforms
  • Experience integrating manufacturing data systems for regulatory compliance, validation, and process optimization.
  • Background spanning multiple disciplines (e.g., engineering, chemistry, biology, manufacturing operations, and regulatory affairs).
  • Individuals with unconventional career paths combining engineering and biological sciences expertise are strongly encouraged to apply.

Must be a US Citizen or a Full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.