Supervisor, FDA Computer System Validation Business Applications Risk Consulting
Philadelphia, PA - USA
Job Summary
We are the leading provider of professional services to the middle market globally our purpose is to instill confidence in a world of change empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled culture and talent experience and our ability to be compelling to our clients. Youll find an environment that inspires and empowers you to thrive both personally and professionally. Theres no one like you and thats why theres nowhere like RSM.
RSMs Business Application Risk Solutions practice specializes in managing governance risk security data and compliance across the full lifecycle of core business applicationsfrom implementation through steady-state operations. We are seeking an experienced Computer System Assurance (CSA) & Data Integrity Supervisor to lead and expand our FDA IT Compliance Validation and Technology Risk practice. This role blends traditional CSV leadership with emerging expectations from FDAs updated CSA guidance (Feb 3 2026) QMSR requirements experience with and working understanding of data integrity principles systems security and controls design and data migration/data quality validation for regulated (GxP) digital systems.
The ideal candidate will provide strategic oversight across the full system lifecyclefrom requirements through regulatory test script design testing data migration and ongoing assuranceto ensure our clients maintain auditready inspectioncredible systems in alignment with FDA expectations.
We are looking for an experiencedValidation Supervisorto develop and grow our FDA IT Compliance and Validation practice.
Key Responsibilities
Regulatory & Quality Leadership
- Interpret and apply FDA CSA Guidance 2026 FDAs QMSR 21 CFR Part 11 Annex 11 and GAMP 5 to client systems and engagements
- Serve as a trusted advisor on GxP compliance data integrity and system assurance best practices
- Assist in development and delivery of training and awareness programs on CSA data integrity QMSR requirements across firm lines of service
Computer System Assurance & Validation Delivery
- Lead the endtoend delivery of CSA/CSV projects including planning execution reporting and inspection readiness
- Oversee creation of riskbased requirements validation strategies traceability matrices protocols testing evidence and summary reports
- Apply FDAs CSA testing philosophy (e.g. unscripted testing ad hoc testing vendor reuse) to maximize efficiency and assurance
- Evaluate proposed changes to validated computer systems and recommend appropriate CSA/CSV activities based on process risk and patient impact
Data Integrity Data Migration and Data Quality Validation
- Partner with service line colleagues in conducting assessments of ALCOA data integrity controls across applications integrations and business processes
- Help define data flow diagrams and system interaction maps that support data integrity and security analyses
Security-by-Design Controls and Risk Management
- Partner with security architects and SOD teams to ensure compliant access models change control processes and control operation testing are in place
- Assess cyber risk impacts on validated systems as part of CSA risk methodology
Project & Team Leadership
- Act as CSA/CSV Lead for client projects; manage internal project resources and coordinate with cross-functional teams.
- Integrate validation activities into broader project timelines in partnership with engagement project managers
- Provide coaching mentoring and oversight to junior validation/assurance consultants
- Support practice development activities including methodology updates templates accelerators and training programs
Required Education and Experience
- 4 years of experience in CSV/CSA data integrity or technology risk roles within FDA-regulated industries or consulting.
- Bachelors degree in Computer Science MIS Engineering Life Sciences or equivalent experience.
- Strong understanding of:
- FDA CSA Guidance (Feb 3 2026)
- FDA QMSR (ISO 13485 alignment)
- 21 CFR Part 11 / Annex 11
- GAMP 5 (2nd Edition)
- 21 CFR 210/211 (as applicable)
- Experience assessing and testing systems for electronic records/e-signatures requirements.
- Handson experience with data integrity assessments data migration validation and SaaS vendor assurance (e.g. NetSuite SAP D365 LMS e-signature platforms).
- Excellent leadership communication presentation and project management skills.
Preferred Qualifications
- Experience with cloud ERP systems (NetSuite SAP D365) in regulated environments
- Familiarity with cybersecurity frameworks (NIST CSF ISO 27001) as they apply to GxP systems
- Prior supervisory or teamlead experience
- Knowledge of security controls SOD and ITGCs as applied to regulated systems
- Experience interacting with FDA or supporting clients during inspections
At RSM we offer a competitive benefits and compensation package for all our offer flexibility in your schedule empowering you to balance lifes demands while also maintaining your ability to serve more about our total rewards at applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal state or local law.
Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/ is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application interview or otherwise participate in the recruiting process please call us at or send us an email at .
RSM does not intend to hire entry level candidates who will require sponsorship now OR in the future (i.e. F-1 visa holders). If you are a recent U.S. college / university graduate possessing 1-2 years of progressive and relevant work experience in a same or similar role to the one for which you are applying excluding internships you may be eligible for hire as an experienced associate.
RSM will consider for employment qualified applicants with arrest or conviction records. For those living in California or applying to a position in California please click here for additional information.
At RSM an employees pay at any point in their career is intended to reflect their experiences performance and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including but not limited to education skills work experience certifications location etc. As such pay for the successful candidate(s) could fall anywhere within the stated range.
Compensation Range: $85100 - $161700Individualsselected for this role will be eligible for a discretionary bonus based on firm and individual performance.
Required Experience:
Manager
About Company
RSM US LLP is the leading U.S. provider of assurance, tax and consulting services focused on the middle market.