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Validation Engineer Biomedical Jobs in Virginia (NOW HIRING)

Senior Specialist, Engineering- Validation

Elkton, VA

$117K - $184K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biomedical engineering, chemical engineering, computer science, integrated science or related life ... CTU/WH qualification / validation; Dry Heat Depyrogenation qualification / validation; Steam ...

$117K - $184K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biomedical engineering, chemical engineering, computer science, integrated science or related life ... CTU/WH qualification / validation; Dry Heat Depyrogenation qualification / validation; Steam ...

Biomedical Technician I

Winchester, VA

$19.50 - $26/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Duties include, but are not limited to, validation and inspection of clinical equipment for ... engineering environment preferred * Travel may be required based on customer or business needs ...

$52K - $72K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biomedical engineer) servicing diagnostic instruments needed. * Valid driver's license, ability to drive independently day and night, and good driving record required. * Physical Requirements:

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biomedical engineer) servicing diagnostic instruments needed. * Valid driver's license, ability to drive independently day and night, and good driving record required. * Physical Requirements:

Biomedical Technician I

Winchester, VA · On-site

$19.40 - $29.90/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Duties include, but are not limited to, validation and inspection of clinical equipment for ... engineering environment preferred * Travel may be required based on customer or business needs ...

$58K - $80K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biomedical engineer) servicing diagnostic instruments needed. * Valid driver's license, ability to drive independently day and night, and good driving record required. * Physical Requirements:

Biomedical Technician I

Hampton, VA

$19.50 - $26/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Biomedical Equipment Technician I (BMET I) provides clinical equipment services under the close ... clinical engineering environment preferred * Valid drivers license required; variable travel ...

Biomedical Technician I

Hampton, VA · On-site

$19.40 - $29.90/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Biomedical Equipment Technician I (BMET I) provides clinical equipment services under the close ... clinical engineering environment preferred * Valid drivers license required; variable travel ...

Biomedical Technician I

Virginia Beach, VA · On-site

$19.50 - $26/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... • Valid driver's license and ability to travel as needed. • A 2-year technical/electronics ... engineering environment preferred. If you're ready to grow your technical career while supporting ...

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Showing results 1-20

Validation Engineer Biomedical information

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

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

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Virginia?

For Validation Engineer Biomedical jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Biomedical jobs in Virginia look for?

The top searched job categories for Validation Engineer Biomedical jobs in Virginia are:

What cities in Virginia are hiring for Validation Engineer Biomedical jobs?

Cities in Virginia with the most Validation Engineer Biomedical job openings:

Infographic showing various Validation Engineer Biomedical job openings in Virginia as of June 2026, with employment types broken down into 2% Internship, 61% Full Time, 14% Part Time, 2% Temporary, 20% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Senior Specialist, Engineering- Validation

MSD

Elkton, VA

$117K - $184K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

Job Description

Primary Responsibilities

  • Providing a leadership and technical supportive role in the areas of Steam Sterilization, Dry Heat Depyrogenation, Steam Decontamination, Vaporized Hydrogen Peroxide Decontamination, Controlled Temperature Unit Temperature Mapping and Warehouse Temperature Mapping Performance Qualification Validation activities (but not limited to);
    • Scheduling and executing PQ Validation activities
    • Scheduling and managing PQ protocol close-outs
    • Performing technical investigations and analyses
    • Driving to and recommending corrective actions and seeing them through to successful/sustainable implementation
    • Reviewing procedural revisions to be compliant with regulatory expectations
    • Data analysis and Second Person Review
    • Troubleshooting activities associated with all aspects of PQ execution
    • Final report and procedure writing and review
    • Change control evaluation / implementation
    • QMS evaluation / alignment
    • SME presentation to regulatory inspectors
    • Directly interfacing with Project / IPT customers to manage pinches / challenges
    • Maintain team accomplishment metrics and present as needed
    • Manage of team of Contractors and / or P1 and P2 employees (including but not limited too)
      • Justifying appropriate team headcount
      • Authoring job postings / conducting interviews / evaluating candidates as needed
      • Assigning / Assisting with prioritization of work responsibilities
      • Evaluating performance and providing regular feedback
      • Sponsoring employee growth and developmental opportunities through routine 1:1 developmental coaching
      • Participating in Year End assessment activities as applicable
      • Sponsoring the team to achieve Safety and Quality compliance excellence
  • Multiple opportunities will be provided to stream-line team performance and effectiveness
  • Multiple opportunities will be provided to grow as both a SME and people manager

Education Minimum Requirement:

  • Bachelor or Master degree in, biology, biochemistry, biochemical engineering, biological systems engineering, biomedical engineering, chemical engineering, computer science, integrated science or related life science or engineering discipline

Required Experience and Skills

  • Minimum five (5) years of pharmaceutical manufacturing industry
  • Working in a cGMP environment
  • Effective problem-solving skills and a hands-on approach to problem solving, with a bias toward going to see problems for oneself in the field
  • Excellent technical, organizational, interpersonal, collaborative, and verbal/written communication
  • Ability to examine an issue from diverse perspectives (safety, compliance, maintenance, automation, equipment, process, and people) in order to best understand and resolve it
  • Enthusiasm, confidence and initiative-taking ability needed for continuous learning and its applications
  • Willingness to work as a contributing member of a dynamic team of individuals
  • Experience acting as a team leader
  • Knowledge and/or experience in: CTU/WH qualification / validation; Dry Heat Depyrogenation qualification / validation; Steam Sterilization / Sanitization qualification / validation; VHP Decontamination qualification / validation

Required Skills:

Biochemistry, Biopharmaceutical Industry, Good Manufacturing Practices (GMP), Pharmaceutical Manufacturing, Steam Sterilization, Sterilization, Sterilization Validation, Temperature Mapping, Validation

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

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The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

08/25/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.