Regulatory Affairs Specialist (contractor)

Boston Scientific Gruppe; Pasig; On-site; PHP 600,000 - 900,000; Full time

Job summary

Boston Scientific Philippines is seeking a Regulatory Affairs Specialist (contractor) to manage regulatory activities for medical devices in the Philippines, including submissions to the FDA Philippines (CDRRHR) and lifecycle management. The role requires coordinating with cross-functional teams to ensure ongoing market access and regulatory compliance.

The ideal candidate has 2+ years in regulatory affairs for medical devices, familiarity with CMDN/CMDR, and experience interacting with FDA

Qualifications

• 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).

Responsibilities

• Support timely product registrations and lifecycle management for medical devices.
• Coordinate with FDA Philippines (CDRRHR) and internal teams on regulatory submissions.
• Provide regulatory guidance on labeling, claims, and promotional materials.
• Collaborate with QA, Supply Chain, Marketing, and regional Regulatory teams on launches and lifecycle activities.
• Maintain regulatory databases and assist audits.

Skills

Regulatory affairs

Regulatory writing

Documentation

Stakeholder management

Cross-functional collaboration

Communication

Education

Bachelor’s degree in Pharmacy / Biology / Medical Technology / Engineering

Licensed Pharmacist (advantage)

Job description

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Regulatory Affairs Specialist (contractor)

Onsite Location(s): Pasig City, Philippines

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.
• 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.
• 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 byprovidinga 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,neurologicaland urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn .

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