Software Validation Associate

Pharmaron


Job Location:

Exton, PA - USA

Monthly Salary: USD 48000 - 50000
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Position: Software Validation Associate

Salary Range: $48k - $50k

Location: Exton PA

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 21000 employees worldwide across 23 locations in the US UK and China we support drug discovery through to manufacturing with fully integrated high-quality services.

Were proud of the impact we make and just last year we supported over 780 discovery projects 1000 CMC programmes and 1000 clinical trials across all phases. Our teams are involved in everything from small molecules ADCs biologics and gene therapies and we work with more than 3000 global customers. To learn more visit .

Job Overview:

Pharmaron is seeking a motivated and detail-oriented Software Validation Associate to join our team in Exton PA. This role offers an exciting opportunity to build expertise in Computerized Systems Validation (CSV) while supporting critical laboratory systems that enable the development of life-changing therapies.

As a Software Validation Associate you will collaborate with Quality IT laboratory operations and system owners to ensure computerized systems and software applications meet regulatory requirements and industry best practices. You will actively participate in all phases of the validation lifecycle including risk assessments validation planning protocol execution documentation development and compliance assessments for GMP and GLP laboratory environments.

Key Responsibilities

  • Support and execute computerized system validation activities throughout the entire system lifecycle for laboratory software and related technologies.
  • Develop review and execute validation documentation including Validation Plans Risk Assessments User Requirements Specifications (URS) Functional Specifications IQ/OQ/PQ protocols Traceability Matrices and final reports.
  • Collaborate cross-functionally with laboratory personnel Quality Assurance IT and system owners to ensure validated systems meet regulatory and business requirements.
  • Participate in risk assessments and identify opportunities to improve validation processes and compliance practices.
  • Review existing validation documentation identify compliance gaps and assist in implementing remediation plans when necessary.
  • Ensure computerized systems remain compliant with applicable regulations and guidance including GAMP ICH USP ALCOA and 21 CFR Part 11.
  • Support software implementation upgrades change controls and periodic reviews within regulated laboratory environments.

What Were Looking For

  • Bachelors degree in Information Technology Computer Science Life Sciences Engineering or a related discipline.
  • Foundational knowledge of GMP GLP GAMP ICH guidelines and 21 CFR Part 11 requirements.
  • Experience with software validation software testing database integration or computerized systems in a regulated environment through industry experience internships or academic projects.
  • Understanding of Software Development Life Cycle (SDLC) principles and validation methodologies.
  • Strong analytical organizational and problem-solving skills.
  • Excellent communication skills and the ability to collaborate effectively across multiple functions.
  • A strong attention to detail and commitment to quality and compliance.

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 21000 employees and operations in the U.S. the U.K. and China. 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:

  • Insurance including Medical Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

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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Required Experience:

IC

Position: Software Validation AssociateSalary Range: $48k - $50kLocation: Exton PAAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21000 employees worldwide across 23 locations...

About Company

Pharmaron provides comprehensive research, development, and manufacturing services across drug discovery, preclinical, clinical, and commercialization.

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