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Validation Associate Jobs (NOW HIRING)

Precigen, Inc

Associate/Validation Engineer

Germantown, MD · On-site

$75K - $105K/yr

We are seeking a Associate / Validation Engineer at our Germantown, MD location to join us in our mission to serve patients with our next generation of innovative Gene Therapies. This position will ...

Clopay

Validation Engineer

Goodyear, AZ

The Engineering Validation Technician is a hands-on, cross-functional role responsible for ... Associate degree or technical training in electrical, mechatronics, or controls is preferred, but ...

DPDHL

Validation Specialist

Westerville, OH

$55K - $90K/yr

Validation Specialist (US-O) The Validation Specialist role has a national salary range of $55,000 ... Associate or bachelor's degree in a related field, preferred * Certification related to quality ...

New

Clopay

Validation Technician

Goodyear, AZ · On-site

The Engineering Validation Technician is a hands-on, cross-functional role responsible for ... Associate degree or technical training in electrical, mechatronics, or controls is preferred, but ...

Fladger Associates

Validation Engineer

Fremont, CA · On-site

Excellent employment opportunity for a Validation Engineer in the Fremont, CA area. * Manage and participate actively in all phases of qualification/validation for QC systems such as QC analytical ...

Intellectt INC

Validation Engineer

Boston, MA · On-site

Position Summary Seeking Validation Engineers (Associate through Senior level) to support execution-heavy validation remediation activities. This is a hands-on role focused on closing validation gaps ...

New

DHL

Validation Specialist

Westerville, OH · On-site

$55K - $90K/yr

Validation Specialist (US-O) The Validation Specialist role has a national salary range of $55,000 ... Associate or bachelor's degree in a related field, preferred * Certification related to quality ...

Clopay Corporation

Validation Engineer

Goodyear, AZ · On-site

$28 - $32/hr

The Engineering Validation Technician is a hands-on, cross-functional role responsible for ... Associate degree or technical training in electrical, mechatronics, or controls is preferred, but ...

Clopay Corporation

Validation Technician

Goodyear, AZ · On-site

The Engineering Validation Technician is a hands-on, cross-functional role responsible for ... Associate degree or technical training in electrical, mechatronics, or controls is preferred, but ...

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How much do validation associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for validation associate in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

How does a Validation Associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.

What are Validation Associates?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

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Validation Associate jobs near you
Associate/Validation Engineer

Associate/Validation Engineer

Precigen, Inc

Germantown, MD • On-site

$75K - $105K/yr

Full-time

Posted 16 days ago

Job description

We are seeking a Associate / Validation Engineer at our Germantown, MD location to join us in our mission to serve patients with our next generation of innovative Gene Therapies. This position will require a professional who is technically savvy, thrives in a dynamic team environment, poses exceptional problem-solving skills, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will provide Validation Engineering support to Precigen’s GMP Manufacturing, Quality Control (QC), and Research and Development (R&D) facilities.


Duties and Responsibilities:

  • Oversee site Validation Program, coordinating with Metrology, Facilities, and User group personnel, as well as external vendors, to ensure the proper qualification status of Facility systems [e.g. Heating Ventilation and Air Conditioning (HVAC), Backup Power, Water Purification, Compressed Gass Distribution, Glass/Part Washers, Autoclaves, Refrigerator/Freezers], Process Equipment [e.g. Incubators, Tangential Flow Filtration (TFF), Fast Protein Liquid Chromatography (FPLC), and Centrifuges], and Analytical Equipment [e.g. Polymerase Chain Reaction (PCR), Environmental Monitoring Equipment, Cell Analysis, Spectrophotometers]. Hand-on troubleshooting, partnership with Original Equipment Manufacturer (OEM) or service vendors, as needed
  • Controlled Temperature Mappings for CTU Qualifications
  • Provide technical expertise to guide formation of qualification requirements for new site systems and update/improvement of existing equipment/utilities per site Validation Master Plan and Procedures
  • Participate on project teams requiring validation support to represent the function internally on specific projects
  • Author and Review Qualification Related Standard Operating Procedures (SOPs), Work Instructions (WI), and Validation Plans
  • Author, Review, and Execution of Validation Protocols and Reports, such as temperature mapping of Controlled Temperature Units (CTUs) and Autoclaves using KAYE validator or similar data logging equipment, Engineering studies, and IQ/OQ/PQ of facility, processing, and analytical equipment
  • Collect, compile and analyze validation data and information with some or minimal supervision, demonstrating ownership of data to confirm the validated state of the equipment for GMP use
  • Support site Quality Management System (QMS) through Authoring and Reviewing of Qualification related Change Controls, Deviations, and Corrective and Preventive Actions (CAPA)


EDUCATION AND EXPERIENCE:

  • Bachelor’s degree in Engineering or Life Sciences and Two (2) + years of Good Manufacturing Practice (GMP) Qualification experience (Level will be determined based on education and experience) with working knowledge of FDA and Eudralex regulations
  • Technical Writing experience generating Standard Operating Procedures (SOP), Protocols/Reports, Work Instructions, and Validation Plans
  • Strong computer skills- familiarity with Microsoft Office, Quality Record Management, Computerized Maintenance Management Systems(CMMS), Building Management/Automation Systems (BMS/BAS), Environmental Monitoring System(EMS), Validation Data Management Software, Computer Aided Design (CAD) and the ability to quickly learn new applications
  • Ability to sit, stand, and walk regularly to access mechanical areas and aseptically gown into production suite. Able to maneuver equipment and supplies up to 40 pounds


EOE MFDV