Validation Specialist Jobs
Validation Specialist jobs are open across pharmaceuticals, medical devices, biotech, and manufacturing, from entry-level to senior and principal levels, with specializations in process validation, computer systems validation, and equipment qualification. Find a role that fits from the openings below and apply directly.
Find Validation Specialist JobsOverview
Showing 5 of 49+ Validation Specialist jobs
INTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The QA Release & Validation Specialist is responsible for reviewing & approving the following:
- Executed batch records & batch disposition
- QC testing assays
- Executed validation documentation
This position reports to the QA Release Supervisor and is part of the QA Release team within the Operational QA organization located in Fargo, ND and will be an on-site role.
In this role, you will have the opportunity to:
- Review production and test records for completeness and accuracy, ensuring data supports release, meets SOP and applicable Regulations, and all deviations have been appropriately investigated and resolved.
- Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable Regulations.
- Serve as the QA subject matter expert and ensure products, testing, and validation activities not meeting specifications are dispositioned appropriately.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- A minimum of one (1) year of experience in a Quality or auditing role
- Experience working in a regulated or GMP-compliant environment.
- Bachelor of Science or life science discipline preferred or equivalent experience.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- US Code of Federal Regulations (CFR) and/or EU Regulations
- cGMP
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- No travel is required as this is an on-site position.
- Ability to use computer, monitor, headset, mouse/keyboard, sit/stand desk, and copier/scanner.
- Ability to lift, move or carry equipment up to 50lbs.
COMPENSATION
The annual salary range OR the hourly range for this role is $43,500.00 - $72,000.00 USD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
INTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The QA Release & Validation Specialist is responsible for reviewing & approving the following:
- Executed batch records & batch disposition
- QC testing assays
- Executed validation documentation
This position reports to the QA Release Supervisor and is part of the QA Release team within the Operational QA organization located in Fargo, ND and will be an on-site role.
In this role, you will have the opportunity to:
- Review production and test records for completeness and accuracy, ensuring data supports release, meets SOP and applicable Regulations, and all deviations have been appropriately investigated and resolved.
- Review Equipment, Process, Computer Validation, and Bioanalytical Method Development Validation executed documentation to ensure compliance with approved protocols, quality standards, and applicable Regulations.
- Serve as the QA subject matter expert and ensure products, testing, and validation activities not meeting specifications are dispositioned appropriately.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- A minimum of one (1) year of experience in a Quality or auditing role
- Experience working in a regulated or GMP-compliant environment.
- Bachelor of Science or life science discipline preferred or equivalent experience.
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- US Code of Federal Regulations (CFR) and/or EU Regulations
- cGMP
Travel, Motor Vehicle Record & Physical/Environment Requirements:
- No travel is required as this is an on-site position.
- Ability to use computer, monitor, headset, mouse/keyboard, sit/stand desk, and copier/scanner.
- Ability to lift, move or carry equipment up to 50lbs.
COMPENSATION
The annual salary range OR the hourly range for this role is $43,500.00 - $72,000.00 USD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
See All 49+ Validation Specialist Jobs
Jump back to the full list of openings and apply to any validation specialist role that fits.
Find Validation Specialist JobsValidation Specialist Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Katalyst Healthcares & Life Sciences9
- A123 Systems3
- SiTime3
- KBI Biopharma2
- Point722
Top Industries Hiring
- Consulting & Professional Services14
- Biotechnology & Pharmaceuticals11
- Construction & Real Estate4
- Electronics & Hardware3
- Science & Research3
What Employers Look For
The qualifications that appear most often in validation specialist jobs.
- Bachelor's degree in life sciences, engineering, or a related technical field
- Experience authoring and executing IQ, OQ, and PQ validation protocols
- Knowledge of FDA 21 CFR Part 11 and GMP or GxP regulatory requirements
- Proficiency with computer systems validation for manufacturing or laboratory software
- Ability to write clear technical documents including validation plans and summary reports
- Familiarity with CAPA processes, deviation management, and change control systems
Tips for Your Validation Specialist Job Search
Tailor your resume to validation protocols
Hiring managers scan for protocol types you've authored or executed. List IQ, OQ, and PQ experience explicitly, name the systems you've validated, and call out any FDA-regulated environments you've worked in rather than describing duties in generic terms.
Earn a CSV or GMP credential
Computer systems validation and GMP compliance certifications set you apart from candidates with matching experience but no formal credential. Completing a recognized validation certification signals you understand regulatory expectations before your first day on the job.
Apply early to roles that fit
Migrate Mate lists validation specialist openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Filter openings by industry vertical
Validation work in pharmaceutical manufacturing differs significantly from software or medical-device validation. Targeting openings in the sector where your protocol experience lives shortens your ramp time and makes your resume far more relevant to the hiring team.
Prepare deviation examples before your interview
Interviewers in regulated industries almost always ask how you've handled a failed qualification run or an unexpected deviation. Walk in with a real example that covers root-cause identification, corrective action, and how the deviation was documented in the final report.
Negotiate scope before you negotiate salary
Before accepting an offer, clarify which systems and product lines you'll own, whether you'll write protocols or execute them, and where the role sits in the change-control process. Scope mismatches are the most common reason validation specialists leave within the first year.
Validation Specialist Jobs: Frequently Asked Questions
Which companies are hiring the most validation specialists?
The companies hiring the most validation specialists right now include Katalyst Healthcares & Life Sciences, A123 Systems, and SiTime, with the largest share of openings in Michigan, California, and North Carolina, based on current listings on Migrate Mate as of June 2026. Pharmaceutical manufacturers, medical device companies, and biotech firms consistently account for the highest volume of postings.
How many validation specialist jobs are remote?
About 10% of validation specialist openings are fully remote or hybrid as of June 2026, though hands-on equipment and process validation roles are far more likely to require on-site presence. Computer systems validation and documentation-heavy compliance roles tend to offer the most flexibility for remote or hybrid arrangements.
How do you become a validation specialist?
Start with a degree in a life science, engineering, or chemistry discipline, then gain hands-on experience in a regulated manufacturing or laboratory environment. Learn to write and execute IQ, OQ, and PQ protocols, study FDA GMP and 21 CFR Part 11 requirements, and seek roles specifically labeled as validation associate or junior validation engineer to build your foundational protocol experience.
Can you get hired as a validation specialist without direct experience?
Yes, but you'll need to demonstrate transferable skills. Quality assurance, laboratory technician, and manufacturing roles in regulated industries give you exposure to the documentation standards, deviation management, and regulatory mindset that validation teams value. Completing a computer systems validation or GMP certificate course before applying also signals genuine intent and closes part of the experience gap.
What does the validation specialist interview process look like?
Most hiring processes involve a recruiter screen, a technical interview with a validation manager or engineer, and a practical discussion of your protocol experience. Expect questions about how you've handled failed qualifications, documented deviations, and managed last-minute scope changes. Some employers add a written exercise where you draft a short protocol or risk assessment to evaluate how you structure technical documents.
Where can I find and apply to validation specialist jobs?
You can find and apply to validation specialist jobs on Migrate Mate, which lists current openings from across the United States. Search the listings to find roles that match your experience and specialization, then apply directly to each one that fits.
See All 49+ Validation Specialist Jobs
Jump back to the full list of openings and apply to any validation specialist role that fits.
Find Validation Specialist Jobs