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Validation Associate Jobs in Pennsylvania (NOW HIRING)

Accupac

Validation Associate

Mainland, PA · On-site

Validation Associate I & II Location: Mainland, PA 19451 Join Our Team: At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care ...

Herren Associates

Navy Validator

Philadelphia, PA · On-site

Company Description Herren Associates is a small entrepreneurial engineering and management ... Herren Associates is looking for highly capable Intermediate Navy Validator that is ready for a ...

Herren Associates

Navy Validator

Philadelphia, PA

Company Description Herren Associates is a small entrepreneurial engineering and management ... Herren Associates is looking for highly capable Intermediate Navy Validator that is ready for a ...

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All JobsValidation Associate JobsValidation Associate Jobs in Pennsylvania

Validation Associate information

See Pennsylvania salary details

$22

$52

$78

How much do validation associate jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for validation associate in Pennsylvania is $52.12, according to ZipRecruiter salary data. Most workers in this role earn between $39.52 and $63.37 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.

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 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.

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 most commonly searched types of Validation jobs in Pennsylvania? The most popular types of Validation jobs in Pennsylvania are:
What are popular job titles related to Validation Associate jobs in Pennsylvania? For Validation Associate jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in Pennsylvania look for? The top searched job categories for Validation Associate jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Validation Associate jobs? Cities in Pennsylvania with the most Validation Associate job openings:
Validation Associate jobs near you
Infographic showing various Validation Associate job openings in Pennsylvania as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $108,412 per year, or $52.1 per hour.

Validation Associate

Accupac

Mainland, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Accupac rating

6.6

Company rating: 6.6 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

Job description

Job Title: Validation Associate I & II
Location: Mainland, PA 19451

Join Our Team:
At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetics, over-the-counter and medical devices across skincare, haircare, oral care, and healthcare products.

But beyond that, we make a difference. We make a difference in the lives of our people, we make a difference in the community around us, we make a difference in the health of our planet for a better, brighter, more beautiful future for all.

We value detail-driven professionals who thrive on accuracy and compliance. As a Validation Associate, you’ll ensure our processes and equipment meet rigorous quality standards and regulatory requirements, keeping products safe and effective for the people who rely on them.

What We Offer:

  • Competitive Pay
    • Salary Range: $44,000.00 - $60,000.00
    • Bonus: Exempt employees are eligible for a bonus in accordance with Accupac’s Bonus Plan.

o The posted job may span more than one career level. The final offer, including level and pay, will be determined based on a variety of factors such as the candidate’s relevant job and industry experience, education, knowledge, skills, geographic location, and abilities. Internal equity and alignment with market data will also be considered. We are committed to providing fair and competitive compensation based on each candidate’s qualifications and fit for the role.

  • Employees are eligible for the following benefits:

o Medical, Dental, and Vision insurance

o Health Savings Account

o Life Insurance with Optional Supplemental Plan

o Pet Insurance

o Short-Term Paid Disability

o 401(k) Retirement Plan with Vested Company Match Contribution

o Paid Time Off (PTO)

o 10 Paid Holidays

o Health Advocacy Programs

Career Growth

What You’ll Do:

  • Review customer documentation to assess required validation activities
  • Write and execute protocols, perform IQ/OQ testing, and maintain validation reports
  • Collaborate with Quality Systems, Project Management, and Operations teams
  • Manage validation documentation in compliance with SOPs and GMP standards
  • Support calibration and preventative maintenance tracking
  • Maintain the Calibration Management database and ensure timely PMs and calibrations
  • Investigate and resolve validation deviations and errors with QA and departmental managers

What We’re Looking For:

  • Bachelor’s degree preferred or 1–4 years of experience in a cGMP-regulated environment
  • Strong organizational and documentation skills
  • Experience with IQ/OQ/PQ validation protocols
  • Familiarity with manufacturing, packaging, and cleaning processes
  • Ability to read, write, and communicate effectively in English
  • Strong attention to detail and ability to work independently
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Ready to Apply?
Join us at Accupac and become part of a company that values your skills and dedication. Click below to apply today!

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