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Validation Associate Jobs in North Carolina (NOW HIRING)

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

Engineer, Cleaning Validation Specialist3 Key Consulting is hiring an Engineer, Cleaning Validation ... Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of ...

New

Engineer, Cleaning Validation Specialist3 Key Consulting is hiring an Engineer, Cleaning Validation ... Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of ...

New

Bachelor's degree in a science or engineering related field OR an Associate's degree in a science or engineering related field with an additional 2-3 years of related process validation experience ...

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Showing results 1-20

Validation Associate information

See North Carolina salary details

$20

$47

$71

How much do validation associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for validation associate in North Carolina is $47.25, according to ZipRecruiter salary data. Most workers in this role earn between $35.82 and $57.45 per hour, depending on experience, location, and employer.

What is a validation associate?

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.

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 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.

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.

What are the most commonly searched types of Validation jobs in North Carolina?

The most popular types of Validation jobs in North Carolina are:

What are popular job titles related to Validation Associate jobs in North Carolina?

For Validation Associate jobs in North Carolina, the most frequently searched job titles are:

What job categories do people searching Validation Associate jobs in North Carolina look for?

The top searched job categories for Validation Associate jobs in North Carolina are:

What cities in North Carolina are hiring for Validation Associate jobs?

Cities in North Carolina with the most Validation Associate job openings:

Infographic showing various Validation Associate job openings in North Carolina as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 23% Part Time, 7% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $98,289 per year, or $47.3 per hour.

$46/hr

Full-time

Re-posted 8 days ago


Job description

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Qualifications

Validation Associate needs BS degree in a technical discipline.


Validation Associate requires:

  • Must have 3-5 years experience with Sterilization Equipment Processing.
  • A combination of Cycle Development; Process Engineering and Validation Engineering
  • cGMP regulations and latest validation guidelines
  • Able to work extended/odd hours around manufacturing schedule as required.
  • aseptic processing and terminal sterilization 
  • strong project management

must
be able to Lift and carry light loads as necessary in conducting
testing, sitting, standing, walking, weekend or long hours based on
testing schedule, wear proper gowning and PPE in manufacturing areas as
required to meeting GMP and OSHA requirements.

Validation Associate duties:

  • Ensure all aspects of validation adhere to required policies and procedures, including safety and training.
  • Writing and execution/coordination of validation protocol testing.
  • Compile and report on relevant validation data and generate summary reports to document the results of the validation studies.



Additional Information

$46hr

12  MONTHS


Global Channel Management logo

About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Year founded

2009

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