NEW JOB OPENING
PLM VALIDATION ANALYST
IN Cary, IL, USA!

 

Date Posted: 08/06/2026
Hiring Organization: Rose International
Position Number: 505296
Industry: Medical Equipment & Supplies
Job Title: PLM Validation Analyst
Job Location: Cary, IL, USA, 60013
Work Model: Onsite
Shift: 1st Shift (CST)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 7
Min Hourly Rate($): 45.00
Max Hourly Rate($): 50.00
Must Have Skills/Attributes: PLM, System Administrator, UAT
Experience Desired: (CSV/CSA) experience validating enterprise systems in FDA/GxP regulated environments (3+ yrs); Validation documentation (URS, FS/DS, RTM, IQ/OQ/PQ, Risk Assessments, Validation Reports) (3+ yrs); PLM implementations (Agile PLM, MasterControl, Windchill, Teamcenter, Arena, or similar) (3+ yrs); Working knowledge of QMS, cGMP, GxP, and 21 CFR Part 11 compliance requirements (3+ yrs)
Required Minimum Education: Bachelor’s Degree

**C2C is not available**

 

Job Description
Required Education:

• Bachelor's degree in Computer Science, Engineering, Business, or a related discipline.



Required Qualifications/Skills/Experience:

• 3+ years of Computerized Systems Validation (CSV/CSA) experience with strong validation document authoring.

• Hands-on experience executing CSV/CSA in a regulated (GxP/FDA) environment.

• Experience authoring validation documentation, including:

User Requirements Specification (URS)

Functional/Design Specifications (FS/DS)

Risk Assessments

Requirements Traceability Matrix (RTM)

IQ/OQ/PQ Test Scripts

Validation Summary Reports

• Experience with User Acceptance Testing (UAT), including test script development, planning, execution, defect tracking, and resolution.

• Experience gathering business requirements and translating them into functional/system requirements.

• Experience supporting Product Lifecycle Management (PLM) implementations.

• Experience validating workflows, system configurations, permissions, integrations, and data mapping.

• Knowledge of Quality Management Systems (QMS), cGMP, GxP, and 21 CFR Part 11 compliance.

• Experience collaborating with cross-functional teams including IT, Business, Quality, and Validation.

• Strong technical documentation, analytical, organizational, and communication skills.

• Ability to work independently in a fast-paced implementation environment.

Preferred Qualifications/Skills/Experience:

• Experience with PLM platforms such as Agile PLM or MasterControl.

• Experience working with software vendors during implementation projects.

• Experience creating process maps, work instructions, job aids, and training documentation.

• Experience supporting change management and user readiness activities.

• Knowledge of testing tools and defect management systems.

• Experience in cGDP-regulated environments.



PLM Validation Analyst Overview:

The PLM Validation Analyst supports the implementation, validation, and configuration of Product Lifecycle Management (PLM) systems within a regulated environment. This role partners with business, IT, quality, and validation teams to gather requirements, support system configuration, execute validation activities, develop compliance documentation, coordinate User Acceptance Testing (UAT), and ensure PLM solutions meet business, quality, and regulatory requirements.



Job Duties:

• Partner with Business Analysts and stakeholders to gather and document business and system requirements.

• Translate business requirements into functional specifications, user stories, and system requirements.

• Support PLM configuration, including workflows, roles, permissions, data mapping, and supporting objects.

• Participate in system demonstrations, configuration reviews, and functional prototype evaluations.

• Develop and execute UAT test scripts and support testing activities.

• Track, document, and resolve testing defects through closure.

• Author and maintain CSV validation documentation (URS, FS/DS, RTM, IQ/OQ/PQ, Risk Assessments, Validation Summary Reports).

• Ensure validation deliverables comply with QMS, GxP, cGMP, and 21 CFR Part 11 requirements.

• Support PLM implementation activities alongside IT, Quality, and project teams.

• Validate system integrations, workflows, configuration changes, and permissions.

• Develop process documentation, work instructions, and job aids.

• Support audit readiness and assist with issue resolution during validation and implementation activities.

• Contribute to training materials and end-user documentation in collaboration with project stakeholders.

  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

Apply Now

 

About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.

Sioe, Consultant

Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.

Melody, Consultant

Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.

Diane, Consultant

Rose is an assembly of people grounded in honesty, truth and dignity for all of its employees and contractors.

Samba, Consultant

Rose International maintained good communication during assignments and are very informative through email and phone calls.

Sade, Consultant

EMPLOYEE COMMENTS

  • We want you to work with us, but don't take our word for it. Take a look at this sampling of employee comments. They speak for themselves.