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Method Validation Specialist Jobs (NOW HIRING)

Quality Agents, LLC

Validation Engineer I

Rockville, MD · On-site

... method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by ...

Quality Agents, LLC

Validation Engineer I

Rockville, MD · On-site

... method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by ...

QRC Group

Validation Specialist

Cidra, PR · On-site

Cidra, Puerto Rico | Posted on 08/06/2026 Validation Specialist with a strong knowledge of ... Familiarized with Gage R&R methodology preferable. * Preferably, familiarized with metrology ...

BioLegend

Validation Specialist

San Diego, CA · On-site

Job Summary The Operations Validation Specialist at BioLegend will perform and administer validation activities associated with equipment, processes, test methods, facilities and software/systems, in ...

Unifin SAS

Validation Specialist

Rochester, NY · On-site

Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make ... methods to assess process capability and compliance. • Reviews and compiles supporting ...

Curia, Inc.

Validation Specialist III

Albuquerque, NM · On-site

Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Develop and deliver technical training and support to personnel on validation methodologies ...

AMRI

Validation Specialist III

Albuquerque, NM · On-site

Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the ... Develop and deliver technical training and support to personnel on validation methodologies ...

Machinify

Quality Validation Specialist

About the Opportunity The Quality Validation Specialist reviews completed outpatient coding ... Collaborates with leadership and operational teams to improve audit methodologies, clarify coding ...

Machinify

Quality Validation Specialist

About the Opportunity The Quality Validation Specialist reviews completed outpatient coding ... Collaborates with leadership and operational teams to improve audit methodologies, clarify coding ...

Unifin SAS

Validation Specialist

Rochester, NY · On-site

Position Summary The Validation Specialist is responsible for supporting and executing validation ... Analyzes validation data using appropriate statistical and scientific methods to assess process ...

Pinnaql

Validation Specialist

Aibonito, PR · On-site

Validation Specialist Key Responsibilities: * Develop, review, and execute Validation Master Plans ... Experience with risk management methodologies, including FMEA . * Knowledge of change control ...

Veg Group

Validation Specialist

Aibonito, PR · On-site

Validation Specialist Key Responsibilities * Develop, review, and execute Validation Master Plans ... Experience with risk management methodologies, including FMEA . * Knowledge of change control ...

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Method Validation Specialist information

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How much do method validation specialist jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for method validation specialist in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

What are popular job titles related to Method Validation Specialist jobs?

For Method Validation Specialist jobs, the most frequently searched job titles are:

Validation Engineer I

Rockville, MD • On-site

Quality Agents, LLC
Biotechnology Research and Development • 11 - 50 employees
Learn more about Quality Agents, LLCexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist will evaluate the equipment/utility/system/procedures used in development, production, and holding of pharmaceutical products and determine a validation approach. The individual should have experience with current US and international regulations, guidance, industry best practice in one of the following areas of validation: facilities, utilities, and equipment qualifications, process validation, analytical method validation, or cleaning validation. The individual will coordinate validation activities with the client and meet timelines. Documents prepared by the validation specialist must be approved by the client. Responsibilities include:


  • Interact with clients and works closely with site manufacturing, engineering, and QA to develop validation documents.
  • Travel to various client sites and work independently to complete tasks.
  • Provide qualification and validation services for cGMP manufacturing equipment, systems, and utilities at client sites.
  • Exposure to validation aspects of facility start-up, redesign/retrofit, and expansion.
  • Writes and executes qualification protocols for a variety of biopharmaceutical equipment and support utilities in accordance with SOPs, master plans, regulatory expectations, and industry standards.
  • Conducts temperature mapping studies, including the operation of kaye dataloggers, or equivalent.
  • Review and approve documented test results and maintain records for later analysis.
  • Assist with non-conformances, investigations, and troubleshooting of equipment, utilities, and systems.
  • Able to read P&IDs, isometric drawings, and As-built drawings.


Skill Level and Requirements:


  • Ability to problem solve and troubleshoot.
  • Technical writing ability and use of Microsoft Word, Excel, Power point, and Project
  • Experience with validation equipment such as the Kaye validator, wireless data loggers, or other monitoring devices is strongly desired.
  • Experience using statistical tools is a plus to analyze data captured during validation studies.


Minimum Requirements:


  • BS in a technical discipline (Engineering, chemistry, microbiology, biology)
  • 0-2 years of experience in at least one of the following areas: equipment/utility qualifications, process validation, analytical method validation, or cleaning validation.
  • Current driver's license and auto insurance


Quality Agents offers a full suite of benefits for full-time employees including:


  • Health, dental and vision insurance
  • Life, AD&D and disability Insurance
  • Health savings account for participants in our health plan
  • 401k retirement plan
  • Paid time off
  • Paid holidays


Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.


Equal Opportunity & Accessibility Statement

Quality Agents, LLC is an equal opportunity employer. We make employment decisions without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other protected characteristic under applicable law. We are committed to providing reasonable accommodations for individuals with disabilities throughout the application and hiring process. If you require assistance or accommodation, please contact us.

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