Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
• Learn more about <a href="https://www.philips.com/a-w/about.html" target="_blank"> our business </a> . <br> • Discover <a href="https://www.philips.com/a-w/about/our-history.html" target="_blank"> our rich and exciting history </a> . <br> • Learn more ab
out <a href="https://www.philips.com/a-w/about/environmental-social-governance/our-purpose" target="_blank"> our purpose </a> . </strong><strong></strong><strong> If you’re in
sity and inclusion <a href="https://www.careers.philips.com/global/en/diversity-and-inclusion" target="_blank"> here </a> . </strong></body></html>

Job Information

Philips Regulatory Affairs Senior Manager - Japan in Tokyo, Japan

Regulatory Affairs Senior Manager

Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.

But it’s not just what we do, it’s who we are. We are 75,000, wonderfully unique individuals, with two things in common: An unwavering sense of purpose and a relentless determination to deliver on our customers’ needs. It’s what inspires us to create meaningful solutions – the kind that make a real difference – when it matters most.

The world and our customers’ needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. That’s why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.

Your role:

Exciting opportunity to lead Cardiac and Endovascular projects of Philips Image-guided Therapy, including novel technologies integrated by therapeutic devices and visualization systems.

  • Develop local regulatory strategy and lead the strategic discussion with related stakeholders, including Business Unit, R&D, Clinical Affairs, and Market Access & Reimbursement to accelerate projects and fast serve patients.

  • Proactively identify risks within regulatory strategies, plans, products and propose alternate approaches.

  • Provide interpretation of local regulations to BU partners and ensure necessary requirements are fully deployed.

  • Stay informed of new regulations and technologies relevant to endovascular therapeutics.

  • Plan and execute product registration aligned with local business needs.

  • Maintain current registration approvals accordingly.

  • Manage interactions with MHLW/PMDA and maintain a productive working relationship.

  • Review and Author product registration/reimbursement document.

  • Proceed regulatory assessment and promotional material review.

  • Oversee product registration and RA administration activities.

  • Drive various transformation/improvement activities.

You're the right fit if:

1. Experience.

  • +10 years’ experience in medical device regulatory affairs

  • Actual experience of authoring Class III/IV medical device SHONIN submission in EVT or relevant devices and received approval.

  • Maintains extensive knowledge of PMD act, ISO 13485.

  • Experience or working knowledge of active medical devices and imaging technologies.

  • Capable of resolving escalated issues arising from day-to-day operation.

2. Skills.

  • Self-motivated and able to prioritize to handle multiple tasks/responsibilities.

  • Bachelor of Science Degree (Master preferred)

  • Fluent in Japanese and English

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 the lives of others.

• Learn more about our business .

• Discover our rich and exciting history .

• Learn more about our purpose . 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 .

DirectEmployers