Senior Regulatory Affairs Specialist

1 month ago


Minneapolis, United States Philips Full time
Job Title
Senior Regulatory Affairs Specialist

Job Description

Looking at the challenges the world is facing today Philips' purpose has never been more relevant. So, whatever your role, if you share our passion for helping others, you'll be working towards creating a better and fairer future for all.

In this role you have the opportunity to

You will prepare comprehensive regulatory strategies and filings for both new and legacy devices including significant device changes. You will clearly communicate strategies to RA management, core teams, and business unit leadership for device change activity. You will design, build, implement, and sustain world-class regulatory affairs recommendations, decisions, and submissions while employing working knowledge of global regulatory requirements.

Your role:

  • Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objectives.
  • Create comprehensive regulatory strategies.
  • Develop and prepare product registration submissions for the US, Canada, EU and support worldwide international submissions as assigned.
  • Review and approve advertising, promotional items and labeling for regulatory compliance.
  • Identify potential regulatory approvals risks based on changes in regulations, standards country specific issues or other unique characteristics of the project.
  • Communicate application progress to internal stakeholders.
  • Collaborate with worldwide colleagues regarding license renewals and updates.
  • Communicate with regulatory agencies as needed.
  • Support the site audit for the responsible products, including NB surveillance audit, FDA inspection, MDSAP audit, and all kinds of unannounced audits etc.
  • Provide audit, CAPA and post market regulatory support as assigned.
You're the right fit if:

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
  • Bachelor's degree or Master's degree in Regulatory Affairs and/or a science related field or equivalent experience in the medical device industry.
  • Minimum 5 years of regulatory approvals and submittal experience (EU MDR, Health Canada, USA (PMA, 510k).
  • Must be able to manage multiple tasks and perform with accuracy and a high attention to detail.
  • Requires strong written, oral and interpersonal skills to be able to effectively compose agency submissions, interface interdepartmentally and complete assignments with minimal supervision.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position.
About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Read more about our employee benefits.


If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

Philips Transparency Details

The pay range for this position is $77,000,000 to $136,000, Annually. The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here.

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

#LI-PHI

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.

  • Minneapolis, United States Laborie Medical Technologies Corp Full time

    We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters - it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we'd like to meet you. We support and empower our employees to grow their careers in an...


  • Minneapolis, Minnesota, United States Mlnneapolis heart institute foundation Full time

    The Minneapolis Heart Institute Foundation (MHIF) is on the lookout for a dedicated Quality & Regulatory Affairs Specialist II to help advance MHIF's mission of eradicating heart and vascular diseases. Our commitment is to enhance cardiovascular health through pioneering research and educational initiatives. With over four decades of experience, MHIF stands...


  • Minneapolis, Minnesota, United States Philips Full time

    About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Philips. As a key member of our regulatory team, you will play a critical role in ensuring compliance with regulatory requirements and facilitating the approval of our medical devices.Key ResponsibilitiesRegulatory Strategy and PlanningDevelop and implement...


  • Minneapolis, Minnesota, United States The Judge Group Full time

    Job SummaryThe Judge Group is seeking a highly skilled Regulatory Affairs Specialist to join our team on a 12-month contract basis. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and providing expert guidance on regulatory matters.Key ResponsibilitiesSupport daily Regulatory Affairs...


  • Minneapolis, Minnesota, United States Laborie Medical Technologies Corp Full time

    At Laborie Medical Technologies, we are committed to enhancing healthcare and preserving human dignity. Our mission drives us to make a significant difference in the lives of patients worldwide. We foster an environment that promotes professional growth and a sense of belonging, empowering our employees to contribute meaningfully to our goals. Our culture...


  • Minneapolis, Minnesota, United States Laborie Medical Technologies Corp Full time

    At Laborie Medical Technologies, we are dedicated to enhancing healthcare and preserving human dignity. Our commitment to making a positive difference in the lives of patients worldwide drives our mission. We foster an environment that promotes professional growth and a sense of belonging, empowering our employees to achieve their career aspirations while...


  • Minneapolis, Minnesota, United States Integer Holdings Corporation Full time

    Company Overview: Integer Holdings Corporation is a leading provider of medical device outsourcing solutions, specializing in the cardiac, neuromodulation, orthopedics, vascular, advanced surgical, and portable medical markets. Our commitment to innovation and quality enhances the lives of patients globally.Core Values: At Integer, we uphold a set of core...


  • Minneapolis, United States Integer Holdings Corporation Full time

    By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success. At Integer, our values are embedded in everything we do. Customer We focus on our customers' success Innovation We create better solutions Collaboration We create success...


  • Minneapolis, Minnesota, United States Inspire Medical Systems I Full time

    Company OverviewINSPIRE MEDICAL SYSTEMSInspire Medical Systems is at the forefront of the medical industry, focused on improving the lives of individuals affected by Obstructive Sleep Apnea (OSA). Our groundbreaking FDA-approved device is designed to reduce the severity of OSA for those who have not found consistent relief through CPAP therapy. We are...


  • Minneapolis, United States Boston Scientific Gruppe Full time

    About the role: The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Acts as a primary Regulatory Affairs representative in Material Controls, Supplier Quality and Medical Electrical Equipment spaces. Additionally, the Associate is responsible for representing...


  • Minneapolis, Minnesota, United States Inspire Medical Systems I Full time

    Company OverviewINSPIRE MEDICAL SYSTEMSInspire Medical Systems is at the forefront of medical innovation, focusing on improving the lives of individuals dealing with Obstructive Sleep Apnea (OSA). Our cutting-edge FDA-approved device is designed to reduce the severity of OSA for those who find limited success with traditional CPAP therapy. We are dedicated...


  • Minneapolis, Minnesota, United States Inspire Medical Systems I Full time

    Company OverviewINSPIRE MEDICAL SYSTEMSInspire Medical Systems stands at the forefront of the medical industry, committed to improving the lives of individuals affected by Obstructive Sleep Apnea (OSA). Our groundbreaking FDA-approved device is designed to reduce the severity of OSA for those who find limited success with traditional CPAP therapy. We...


  • Minneapolis, Minnesota, United States Boston Scientific Gruppe Full time

    About Us:At Boston Scientific Gruppe, we are dedicated to enhancing lives through innovative medical solutions. Our advanced products and technologies play a crucial role in diagnosing and treating a variety of medical conditions. We are committed to continuous innovation in key sectors and expanding our reach into emerging markets.In the field of Rhythm...


  • Minneapolis, Minnesota, United States Boston Scientific Gruppe Full time

    About Boston Scientific Gruppe:At Boston Scientific, we are dedicated to enhancing lives through innovative medical solutions. Our advanced products and technologies play a crucial role in diagnosing and treating a variety of medical conditions. We are committed to continuous innovation in key areas and expanding our reach into new markets.In the Rhythm...


  • Minneapolis, Minnesota, United States Integer Holdings Corporation Full time

    Company Overview: Integer Holdings Corporation is a leading global provider of medical device outsourcing solutions, dedicated to enhancing patient care through innovative technologies. Our commitment to quality and excellence drives our success in the cardiac, neuromodulation, orthopedics, vascular, advanced surgical, and portable medical markets.Core...


  • Minneapolis, Minnesota, United States Jack Link's Protein Snacks Full time

    Job OverviewThe Legislative Affairs Specialist will be instrumental in developing, managing, and executing the company's advocacy and policy initiatives within the CPG sector. This position requires interaction with government officials, regulatory bodies, and industry associations to promote and safeguard Jack Link's interests. The role also encompasses the...


  • Minneapolis, Minnesota, United States Coloplast Full time

    Senior Manager, Medical AffairsLocation:Minneapolis, MN, US Job Family: Research & DevelopmentCountry/Region: United StatesThis position is member of the clinical science & office of medical affairs team. is the role is responsible for managing the medical affairs teams for Men's Health and Women's Health, as well as driving and managing clinical...


  • Minneapolis, United States Coloplast Full time

    Senior Manager, Medical Affairs Location: Minneapolis, MN, US Job Family: Research & Development ...


  • Minneapolis, United States Surescripts Full time

    Job Summary:The Associate General Counsel, Regulatory Legal (the "AGC") leads the Regulatory Legal vertical within the Legal Affairs Team. This vertical manages healthcare and privacy regulatory legal issues and intellectual property for Surescripts. The AGC provides front-line regulatory legal counsel for current products and evolving product ideas. The AGC...


  • Minneapolis, United States Boston Scientific Gruppe Full time

    You’ll discover a place where you can have meaningful purpose, improving lives through your life's work. Our products and technologies are used to diagnose or treat a wide range of medical conditions. We continue to innovate in key areas and are extending our innovations into new geographies and high-growth adjacency markets. In Rhythm Management (RM) we...