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Validation Associate Jobs in Pennsylvania (NOW HIRING)

Pharmaron

Software Validation Senior Associate

Exton, PA · On-site

$75K - $85K/yr

Software Validation Senior Associate Salary Range : $75,000-$85,000 Location : Exton, PA (Onsite) About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO ...

Pharmaron

Software Validation Senior Associate

Exton, PA · On-site

$75K - $85K/yr

Software Validation Senior Associate Salary Range : $75,000-$85,000 Location : Exton, PA (Onsite) About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO ...

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 ...

Frontage Laboratories

Associate Scientist

Exton, PA · On-site

Associate Scientist (Pharmacokinetics) - Biologics Location: 760 Pennsylvania Dr, Exton, PA 19341 ... Develop, optimize, and validate ligand binding assays (e.g., ELISA, MSD, Gyrolab) for quantifying ...

Wawa, Inc.

WBC HR Generalist

Media, PA · On-site

Establish a repeatable training and certification framework that validates Associate capability, supports consistent execution of production standards, and creates clear accountability for ongoing ...

Wawa

WBC HR Generalist

Wawa, PA

Establish a repeatable training and certification framework that validates Associate capability, supports consistent execution of production standards, and creates clear accountability for ongoing ...

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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 Sep 2, 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 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 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 August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $108,412 per year, or $52.1 per hour.

Software Validation Senior Associate

Pharmaron

Exton, PA • On-site

$75K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago

Job description

Position: Software Validation Senior Associate
Salary Range: $75,000-$85,000
Location: Exton, PA (Onsite)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
Are you an experienced Computerized Systems Validation (CSV) professional with a passion for quality, compliance, and project leadership? We're seeking a Software Validation Senior Associate to support our GxP laboratories by leading software validation initiatives that ensure regulatory compliance, system reliability, and operational excellence.
In this highly visible role, you'll manage the complete software validation lifecycle while partnering with laboratory operations, Quality, IT, and system owners to validate computerized systems supporting pharmaceutical and biotechnology research and development.
If you're looking for an opportunity to combine technical expertise, project management, and regulatory compliance in a collaborative, science-driven environment, we'd love to hear from you.
As a Software Validation Senior Associate, you'll lead and support Computerized Systems Validation (CSV) projects from initiation through completion while ensuring compliance with FDA, GAMP, ICH, and global regulatory expectations.
Key Responsibilities
  • Lead the full Computerized Systems Validation (CSV) lifecycle for GxP laboratory software and computerized systems.
  • Develop validation strategies, validation plans, risk assessments, protocols, reports, and supporting documentation.
  • Author and execute Software Development Life Cycle (SDLC) documentation including:
    • User Requirements Specifications (URS)
    • Functional and Design Specifications
    • Risk Assessments
    • Traceability Matrices
    • Installation Qualification (IQ)
    • Operational Qualification (OQ)
    • Performance Qualification (PQ)
  • Partner with system owners and cross-functional teams to develop compliant validation documentation and implementation plans.
  • Define project scope, timelines, milestones, deliverables, and resource requirements for CSV initiatives.
  • Track project progress, facilitate status meetings, and provide regular updates to leadership.
  • Support software implementations, upgrades, system enhancements, and change controls while ensuring continued GxP compliance.
  • Review existing validation documentation, identify compliance gaps, and execute remediation plans.
  • Author and maintain Quality System documentation including SOPs, Change Controls, CAPAs, and validation procedures.
  • Serve as a subject matter expert during internal and external regulatory inspections.
  • Monitor evolving FDA, GAMP, ICH, USP, and global regulatory requirements to maintain an effective validation program.

What We're Looking For
  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related technical discipline (or equivalent experience).
  • Minimum of 3 years of Computerized Systems Validation (CSV) experience within pharmaceutical, biotechnology, CRO, or other regulated GxP environments.
  • Hands-on experience developing, executing, and documenting validation protocols and software qualification activities.
  • Strong project management experience leading multiple validation initiatives simultaneously.
  • Experience preparing and maintaining SDLC validation documentation including URS, Functional Specifications, Design Specifications, Risk Assessments, IQ/OQ/PQ Protocols, Traceability Matrices, and Validation Reports.
  • Working knowledge of ERP, laboratory software, and computerized systems used in regulated environments.
  • Excellent technical writing, documentation, and communication skills.
  • Strong organizational, analytical, and problem-solving abilities.
  • Experience supporting FDA, client, or international regulatory inspections.
  • Experience validating laboratory systems, analytical instruments, LIMS, CDS, ELN, or other GxP computerized systems.
  • Knowledge of software implementation, system upgrades, and change management processes.
  • Computerized Systems Validation (CSV)
  • GAMP 5
  • ICH Guidelines
  • FDA 21 CFR Part 11
  • 21 CFR Parts 58, 210, and 211
  • Risk-based validation methodologies
  • GxP compliance requirements
  • Quality Systems and Change Control processes

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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