Regulatory Affairs Specialist (contractor)

Reposted 16 Days Ago
Be an Early Applicant
Pasig, Eastern Manila District, National Capital Region, PHL
In-Office
Junior
Healthtech
The Role
Manage regulatory activities to secure and maintain market access for medical devices in the Philippines. Prepare and submit registrations (CMDN, CMDR), maintain technical documentation and approvals, liaise with FDA Philippines (CDRRHR), support post-market surveillance and audits, and collaborate with cross-functional teams on labeling, claims, and compliance.
Summary Generated by Built In

Additional Locations:  N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

 

Position Overview

The Regulatory Affairs Specialist for Medical Devices is responsible for managing regulatory activities required to ensure timely approval, compliance, and continued market access of medical device products in the Philippines. This includes overseeing product registrations with the Philippine FDA – Center for Device Regulation, Radiation Health, and Research (CDRRHR), maintaining regulatory compliance throughout the product lifecycle, and supporting cross-functional teams on regulatory and technical matters.

Key Responsibilities

1. Regulatory Strategy & Compliance

  • To support timely product approvals and market access for medical devices.
  • Ensure full compliance with Philippine FDA (CDRRHR) regulations and relevant local administrative orders.
  • Monitor regulatory changes and interpret their impact on current and future products; communicate updates to internal stakeholders.

2. Product Registration & Lifecycle Management

  • Prepare, review, submit, and follow up on regulatory submissions (CMDN, CMDR, variations, and renewals).
  • Compile and validate technical documentation
  • Track and maintain regulatory approvals, licenses, and product documentation throughout the product lifecycle.
  • Maintain accurate and up-to-date regulatory databases and records.
  • Support internal and external audits related to regulatory compliance.

3. Government Liaison & External Engagement

  • Serve as a liaison with FDA Philippines (CDRRHR) to facilitate regulatory interactions.
  • Manage regulatory communications, including responses to queries, deficiency letters, and compliance issues.
  • Represent the company in government audits, regulatory inspections, and industry association meetings.

4. Cross-functional Collaboration

  • Collaborate with Commercial, Quality Assurance, Supply Chain, Marketing, and Regional Regulatory teams to support product launches and lifecycle activities.
  • Provide regulatory guidance on claims, labeling, promotional materials, and device modifications.
  • Support internal and external audits related to regulatory compliance.

 

5. Post-Market Surveillance & Compliance

  • Coordinate with QA for post-market surveillance (PMS) requirements and ensure timely reporting to FDA.

Qualifications

Education

  • Bachelor’s degree in Pharmacy, Biology, Medical Technology, Engineering, or related life-science field.
  • Licensed Pharmacist or equivalent professional license is an advantage.

Experience

  • Minimum 2 years of regulatory affairs experience in the medical device industry.
  • Strong understanding of Philippine regulatory pathways (CMDN, CMDR).
  • Experience interacting with FDA Philippines (CDRRHR) is required.
  • Exposure to ISO 13485, AMDD, and global medical device standards is highly preferred.

Skills & Competencies

  • Strong regulatory writing and documentation skills.
  • Solid understanding of medical device technical files and regulatory requirements.
  • Excellent communication and stakeholder management skills.
  • Ability to manage multiple priorities under tight timelines.
  • Strong analytical thinking and problem-solving capabilities.
  • High attention to detail and organizational skills.

Key Attributes

  • Strong Integrity and compliance mindset
  • Proactive and highly organized
  • Ability to influence and collaborate cross-functionally
  • Adaptable in a fast-paced and regulated environment

Requisition ID: 631359


Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Skills Required

  • Bachelor's degree in Pharmacy, Biology, Medical Technology, Engineering, or related life-science field
  • Licensed Pharmacist or equivalent professional license
  • Minimum 2 years of regulatory affairs experience in the medical device industry
  • Experience interacting with FDA Philippines (CDRRHR)
  • Strong understanding of Philippine regulatory pathways (CMDN, CMDR)
  • Exposure to ISO 13485, AMDD, and global medical device standards
  • Strong regulatory writing and documentation skills
  • Solid understanding of medical device technical files and regulatory requirements
  • Excellent communication and stakeholder management skills

Boston Scientific Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Boston Scientific and has not been reviewed or approved by Boston Scientific.

  • Healthcare Strength Healthcare coverage is positioned as comprehensive, spanning medical, dental, vision, life, and disability insurance alongside mental health resources. Family planning support and broader care navigation offerings further strengthen the health-related value of the package.
  • Retirement Support Retirement benefits stand out through a 401(k) match described as best-in-class and supported by profit sharing and an employee stock purchase plan. High participation in retirement programs is also highlighted as part of the overall financial benefits footprint.
  • Leave & Time Off Breadth Time off is described as generous, with reports of 20+ vacation days and up to four weeks in some roles, plus paid holidays and sick leave. Longer-term options such as extended unpaid family leave and a personal enrichment sabbatical expand flexibility beyond standard PTO.

Boston Scientific Insights

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The Company
HQ: Marlborough, MA
52,374 Employees
Year Founded: 1979

What We Do

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 40 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of health care. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. For more information, visit www.bostonscientific.com and connect with us on X, Instagram, and Facebook. At Boston Scientific, you will find purpose, a place to grow and opportunities to cultivate your passions. To search and apply for open positions, visit https://bostonscientific.eightfold.ai/careers. You may also review our social media guidelines at http://www.bostonscientific.com/social.

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