Regulatory Affairs Program Manager

Philips

Regulatory Affairs Program Manager optimizing compliance monitoring and reporting efficiency. Leading regulatory excellence projects at Philips to enhance performance and compliance.

Posted 4/24/2026full-timePlymouth • Massachusetts, Minnesota • 🇺🇸 United StatesMid-LevelSenior💰 $127,500 - $190,000 per yearWebsite

About the role

Key responsibilities & impact

The Regulatory Affairs Program Manager is responsible to optimize regulatory compliance monitoring and reporting efficiency
Implementing robust systems and processes to ensure accurate and timely tracking of regulatory activities
Leading regulatory excellence and continuous improvement projects and programs
Serves as a key liaison with external and internal stakeholders
Undertakes comprehensive evaluations of the organization to assess its current level of regulatory excellence maturity, identifying strengths, weaknesses, and opportunities for improvement.
Maintains key regulatory policies and guidances for the enterprise related to lifecycle management, refurbishment, remanufacturing, and supply chain.
Utilizes project and program management skills to lead projects focused on regulatory compliance and process improvement to enhance performance and drive organizational change.
Represents Regulatory Affairs Centralized Services in regulatory audits and certification meetings, participates in resolving audit findings, and ensures the appropriate deployment of Regulatory Affairs related processes and documents across the QMS.

Requirements

What you’ll need

Bachelor's Degree in Business Administration, Legal, Communications, Science or equivalent
Masters degree preferred
RAPS RAC, CAPM, Six Sigma, CCMP certifications desired
5+ years of experience with Bachelor's OR Minimum 3 years of experience with Master's in areas such as Regulatory Strategy, International Regulations, Medical Device Regulations, Project Management, Continuous Improvement or equivalent
Preferred experience: One or more years of experience with validation of software tools, leading regulatory compliance within the service, refurbishment, and supply chain domains, using regulatory information management (RIM) tools, and UDI machine to machine software.
US work authorization is a precondition of employment.

Benefits

Comp & perks

generous PTO
401k (up to 7% match)
HSA (with company contribution)
stock purchase plan
education reimbursement

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory complianceregulatory strategyproject managementcontinuous improvementregulatory information management (RIM)validation of software toolsmedical device regulationslifecycle managementsupply chain managementaudit resolution

Soft Skills

leadershipcommunicationstakeholder managementorganizational change managementevaluation and assessmentproblem-solvingcollaborationprocess improvementattention to detailstrategic thinking

Certifications

RAPS RACCAPMSix SigmaCCMP