Full-Time

Business Compliance Officer

Posted on 11/26/2025

Philips

Philips

Manufactures sleep therapy and respiratory devices

Compensation Overview

$158k - $252k/yr

+ Annual incentive bonus

No H1B Sponsorship

Cambridge, MA, USA + 1 more

More locations: Malvern, PA, USA

Hybrid

Hybrid: office presence required, at least 3 days per week.

Category
Legal & Compliance (2)
,
Requirements
  • Five or more years of experience as a Compliance Officer, ideally in a healthcare provider-based field.
  • Hands-on experience managing compliance operations under a Corporate Integrity Agreement and ensuring adherence to federal healthcare program requirements.
  • Subject matter expertise in Anti-Kickback Statute considerations, Centers for Medicare and Medicaid Services regulations, claims audits, billing, coding, revenue integrity, medical records, and data analytics.
  • Bachelor’s degree is required; Master’s degree in Law, Health, Business Administration, Risk Management or equivalent with a Juris Doctorate is a bonus but not required.
  • Must be able to meet minimum physical, cognitive, and environmental job requirements with or without accommodation.
  • US work authorization is required and the company will not sponsor work visas.
  • Relocation benefits are not provided; candidate must reside in or commute to Malvern, Pennsylvania or Cambridge, Massachusetts.
  • Strong communication skills and ability to collaborate in a matrixed environment.
  • Experience leading teams under a CIA.
  • Proficiency in Microsoft Office applications, including Excel and PowerPoint.
Responsibilities
  • Oversee CIA obligations and provide compliance guidance on issues facing sales, services, billing and reimbursement, and interactions with healthcare providers and professionals.
  • Lead and be responsible for overall performance, operation, and success of Philips BioTel AM&D’s compliance program, using seven elements.
  • Develop, implement, and maintain policies and procedures that support the effective operation of the Compliance Program and promote adherence to legal, regulatory, and ethical standards. Oversee key compliance activities, including the administration of the “Speak Up” hotline, exclusion list screening processes, and timely completion of required reporting both internal and external.
  • Serve as a primary compliance resource, collaborating with departments such as Human Resources, IT, Sales, and Marketing to provide guidance on healthcare compliance matters.
  • Lead and coordinate compliance education and training initiatives, with a focus on federal healthcare program requirements, independent diagnostic testing facility regulations, and fraud and abuse laws, including the Anti-Kickback Statute and the Federal False Claims Act.
  • Oversee and coordinate routine and ad hoc internal and external compliance reviews, audits, and monitoring activities to evaluate ongoing adherence to the Compliance Program and the Corporate Integrity Agreement.
  • Manage the day-to-day operations of the compliance function, including staff oversight, and identify areas of potential risk or vulnerability.
  • Analyze compliance metrics, communicate findings to leadership and the Compliance Committee, and develop corrective action plans to address issues and prevent recurrence.
  • Continuously monitor the effectiveness of the Compliance Program and implement improvements to enhance its impact and alignment with Company expectations.
  • Respond promptly to alleged violations of laws, regulations, policies, and the Code of Business Conduct by overseeing or conducting objective investigations from intake through resolution.
  • Act as an independent reviewer to ensure compliance concerns are appropriately evaluated, investigated, and resolved in collaboration with relevant departments.
  • Build and maintain strong working relationships with internal and external stakeholders, including in-house and external legal counsel, to effectively address and resolve compliance issues.
Desired Qualifications
  • Master’s degree in Law, Health, Business Administration, Risk Management or equivalent with Juris Doctorate is a bonus but not required.
  • Working knowledge of LEAN processes.
  • Proficiency in Microsoft Office applications, including Excel and PowerPoint.
  • Demonstrated experience delivering educational and compliance program presentations.
  • Experience leading and supporting teams under a Corporate Integrity Agreement, with hands-on experience managing compliance operations and ensuring adherence to federal healthcare program requirements.
  • Subject matter expertise in AKS considerations, CMS regulations, claims audits, billing, coding, revenue integrity, medical records, and data analytics.

Philips Respironics designs sleep and respiratory care devices, including CPAP and BiPAP machines, ventilators, and oxygen concentrators, plus related systems. These devices deliver regulated air pressure, support or assist breathing, and provide concentrated oxygen, often paired with software and data tools for monitoring. The division differentiates itself through its long history within Philips and its integrated ecosystem that connects devices with analytics and clinical support across hospital, clinic, and home settings. Its goal is to improve quality of life and clinical outcomes for people with sleep and respiratory conditions by offering reliable devices, patient support, and data-driven care.

Company Size

N/A

Company Stage

Acquired

Total Funding

$5.1B

Headquarters

Murrysville, Pennsylvania

Founded

1891

Simplify Jobs

Simplify's Take

What believers are saying

  • BioTelemetry acquisition in 2020 expands remote heart monitoring.
  • $479 million settlement in September 2023 closes US litigation.
  • New silicone foam validated safe, enabling global device sales.

What critics are saying

  • ResMed seizes US sleep market share within 6-12 months.
  • FDA consent decree blocks US sales until after 2026.
  • January 2024 US ventilation exit halves revenue permanently.

What makes Philips unique

  • Pioneered CPAP therapy as standard for sleep apnea since 1976.
  • Leads in non-invasive ventilation and home respiratory support.
  • Integrates devices with software for data-driven clinical outcomes.

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Benefits

Health Insurance

401(k) Retirement Plan

401(k) Company Match

Unlimited Paid Time Off

Health Savings Account/Flexible Spending Account

Company News

HIT Consultant
Apr 12th, 2024
Philips Respironics Reaches Final Agreement With Us Regulators On Sleep Apnea Device Recall

<img src="https://hitconsultant.net/wp-content/uploads/2024/04/Philips.webp" alt="Philips Respironics Reaches Final Agreement with US Regulators on Sleep Apnea Device Recall. " class="wp-image-78777" srcset="https://hitconsultant.net/wp-content/uploads/2024/04/Philips.webp 700w, https://hitconsultant.net/wp-content/uploads/2024/04/Philips-300x161.webp 300w, https://hitconsultant.net/wp-content/uploads/2024/04/Philips-290x155.webp 290w" sizes="(max-width: 700px) 100vw, 700px">What You Should Know: – Philips Respironics, a subsidiary of Royal Philips, has finalized a consent decree with the US Department of Justice (DOJ) and Food and Drug Administration (FDA) to address issues raised during a 2021 inspection of a Philips facility in Pennsylvania.– The agreement focuses on Philips Respironics’ operations in the US, particularly regarding the recall of certain sleep and respiratory care devices.– The company’s focus will now be on completing remediation efforts, ensuring patient safety, and regaining regulatory approval to resume sales of new devices in the US.Focus on Remediation and ComplianceThe consent decree outlines a roadmap for Philips Respironics to:Prioritize Recall Remediation: Philips will continue efforts to remediate millions of sleep apnea and respiratory care devices recalled in June 2021 due to potential health risks associated with degraded sound abatement foam.Independent Oversight: Independent experts will be brought in to review recall remediation efforts and ensure Philips Respironics’ business operations comply with FDA regulations.Continued Patient Support: Philips Respironics can continue servicing existing devices in the hands of patients and healthcare providers. Additionally, they can sell accessories, consumables, and replacement parts for these devices.Sales Restrictions Remain in USThe FDA has not yet authorized Philips Respironics to resume sales of new CPAP, BiPAP, or other respiratory care devices in the US. This restriction will remain in place until Philips meets the requirements outlined in the consent decree.Global Sales Continue with RestrictionsPhilips Respironics can continue to sell new devices, accessories, consumables, and replacement parts outside the US,  subject to specific requirements.Safety of Devices with New Foam ConfirmedPhilips Respironics has conducted tests on devices using a new silicone sound abatement foam and found no safety issues. Patients can continue to use these devices following the instructions for use.Financial ImpactPhilips anticipates incurring costs associated with remediation activities and profit disgorgement related to US sales. These costs are estimated at 100 basis points in 2024.  The company’s previously announced 2023-2025 financial outlook remains unchanged,  already factoring in the consent decree. “Strengthening patient safety and quality remains Philips’ highest priority and the increased scrutiny will help us to improve even more

Goodrich Pharmacy
Jan 29th, 2024
Phillips Suspends U.S. Sales of CPAP, Ventilator Machines After Recall

Following a recall of millions of its breathing machines that began in mid-2021, Phillips Respironics announced Monday that it would halt sales of all such machines within the United States.

Parker Waichman LLP
Mar 23rd, 2023
Sleep Apnea Patients Suffer While Waiting To Receive Their Repaired Philips CPAP Machines

In June of 2021, Philips began a recall of over five million of its breathing devices due to toxic fume and substances emanating from the devices’ sound abatement foam.

Digital Journal
Jan 13th, 2023
Ultrasound Market Share | Market | Report | Analysis 2032 | Key Players: Fujifilm Holdings Corporation, Analogic Corporation, Siemens Healthcare among others

February 2019 – Koninklijke Philips launched the EPIQ Elite ultrasound system in the market.

VentureBeat
Oct 26th, 2022
Philips Norelco Brings Movember To Roblox With Shavetopia

Register now for your free virtual pass to the Low-Code/No-Code Summit this November 9. Hear from executives from Service Now, Credit Karma, Stitch Fix, Appian, and more. Learn more. Philips Norelco is creating an interactive metaverse experience called Shavetopia in Roblox, based around the Movember trend. For anyone who doesn’t know what that is, Movember is where people grow facial hair for the entire month of November. The portmanteau comes from adding the word mustache to the name of the month

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