ZipRecruiter

Log In

1

Software Validation Associate Jobs (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 ...

Pharmaron

Software Validation Senior Associate

Exton, PA · On-site

$75K - $85K/yr

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 ...

Sciton

Associate Software V&V Engineer

Palo Alto, CA · On-site

$70K - $80K/yr

Ensures new products are verified and validated prior to shipment release and meet user needs and ... Associate Software V&V Engineer LOCATION Palo Alto, CA (HQ) #J-18808-Ljbffr

Sciton

Associate Software V&V Engineer

Palo Alto, CA · On-site

$70K - $80K/yr

Ensures new products are verified and validated prior to shipment release and meet user needs and ... Associate Software V&V Engineer LOCATION Palo Alto, CA (HQ) Pay Range: $70,000 - $80,000 per year

Sagemcom

Lab QA Technician - Software Validation M/F

Dallas, TX · On-site

$19.50 - $24.75/hr

Lab QA Technician - Software Validation M/F Lab QA Technician - Software Validation M/F Contrat CDI ... Associate or Bachelor's degree in Electronics, Electrical Engineering, or a related technical field.

next page

Showing results 1-20

All JobsTechnology JobsSoftware JobsSoftware Validation Associate Jobs

Software Validation Associate information

See salary details

$10

$56

$98

How much do software validation associate jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for software validation associate in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

What cities are hiring for Software Validation Associate jobs?

Cities with the most Software Validation Associate job openings:

What states have the most Software Validation Associate jobs?

States with the most job openings for Software Validation Associate jobs include:

What are popular job titles related to Software Validation Associate jobs?

For Software Validation Associate jobs, the most frequently searched job titles are:

Infographic showing various Software Validation Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $117,123 per year, or $56.3 per hour.

Software Validation Senior Associate

Exton, PA • On-site

Pharmaron
Chemical Manufacturing • 10K+ employees
Learn more about Pharmaronexternal

$75K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 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.
#LI-PR1

Apply