Spectranetics

Senior Regulatory Affairs Specialist

Spectranetics$105K — $168K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience in medical device regulatory affairs, including 510(k) and EU MDR Technical Documentation authoring.
  • Experience with SaMD or SiMD submissions preferred; international submissions experience is a plus.
  • Strong understanding of relevant regulations and standards (FDA QSR, ISO 13485, ISO 14971, IEC 62304).
  • Bachelor’s or Master’s Degree in a science, engineering, or health-related discipline; RAPS certification is a plus.
  • Excellent communication skills to influence cross-functional stakeholders effectively.

Responsibilities

  • Collaborate with regulatory teams to secure timely product clearances for ultrasound devices.
  • Prepare and coordinate regulatory submission documents for agencies like the FDA and Health Canada.
  • Guide cross-functional teams on regulatory issues throughout product development phases.
  • Lead global regulatory intelligence initiatives and contribute to registration strategies.
  • Act as the Regulatory Affairs representative for BG Ultrasound, focusing on labeling and marketing compliance.

Benefits

  • Comprehensive Philips Total Rewards benefits program including generous PTO.
  • 401k plan with up to 7% match and HSA contributions from the company.
  • Stock purchase plan and education reimbursement opportunities.
  • Commitment to a culture of health and wellness within the workforce.
Full Job Description
Job Title
Senior Regulatory Affairs Specialist

Job Description

Senior Regulatory Affairs Specialist, Ultrasound

The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities include coordinating and preparing regulatory submission documents for agencies such as the FDA, Health Canada, EU Competent Authorities, NMPA, and ANVISA, and offering strategic guidance on clinical studies and evaluations.

Your role:

  • Act as an ambassador of Philips values and ensure compliance with all relevant business processes and regulatory procedures.
  • Serve as the Regulatory Affairs representative for BG Ultrasound, providing guidance on regulatory issues related to product development, labeling, and marketing strategies.
  • Coordinate and prepare documentation for regulatory submissions—such as Product Reports, Technical Files, Declarations of Conformity, and Medical Device Licenses—for various global markets.
  • Support cross-functional teams with regulatory expertise during the design and development phases for new products and major changes to existing products.
  • Lead global regulatory intelligence initiatives, contribute to regulatory and product registration strategies, and help implement global regulatory roadmaps based on the competitive landscape and marketing objectives.

You're the right fit if:

  • You’ve acquired 5+ years of experience in medical device regulatory affairs, with 510(k), and EU MDR Technical Documentation authoring experience required. Experience with SaMD or SiMD submissions is strongly preferred. International submissions experience is a plus.
  • You have strong understanding of relevant regulations and standards (FDA QSR, ISO 13485, ISO 14971, IEC 62304, and other applicable regulations and standards related to software medical devices is preferred. Experience with software development life cycle, artificial intelligence, data science, and/or software testing is preferred.
  • You have a Bachelor’s/Master’s Degree in a science, engineering, or health-related discipline. RAPS certification is a plus.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
  • You’re an excellent communicator, with an ability to influence cross-functional stakeholders utilizing your regulatory expertise. You are willing and able to travel up to 10% based on business needs.

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an office-based role.

The pay range for this position in Murrysville, PA is 94,000 to $150,000.

The pay range for this position in Plymouth, MN is $99,000 to $157,000.

The pay range for this position in Cambridge, MA, Washington D.C., or Bothell, WA is $105,000 to $168,000.

The actual base pay offered may vary within the posted ranges 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 .

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.

Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to one of the posted locations.

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About Spectranetics

Spectranetics is a medical device company that develops, manufactures, and markets single-use medical devices used in minimally invasive procedures within the cardiovascular system. The company's products include laser atherectomy systems, thrombectomy systems, and lead management accessories. Spectranetics was founded in 1984 and is headquartered in Colorado Springs, Colorado. In 2017, the company was acquired by Royal Philips for $2.2 billion.
Learn more about Spectranetics
Size
900 employees
Industry
Founded
1980

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