Integrity without compromise

Every day our products and services help to save lives 
around the globe. Therefore, we make quality and 
reliability our number one priority. 

Get to know us and join our team as

RAQA Manager (m/f/d)

Job Function:  Patient Health & Regulatory Affairs
Location: 

Taguig City, PH, 1636

Work Location (for field-based positions): 
Work Flexibility:  Hybrid
Job ID:  5295

Your Mission

Regulatory Affairs and Quality Assurance

  • Ensure company operations comply with applicable regulatory requirements, including FDA Philippines regulations and other relevant government standards.
  • Prepare, compile, and submit regulatory dossiers and applications (registrations, notifications, variations, and reports) to the FDA Philippines in accordance with regulatory timelines and company requirements.
  • Manage post-market surveillance activities, including monitoring and reporting of complaints, adverse events, CAPA, FSCA, and product recalls until proper closure and documentation.
  • Support and maintain the ISO 9001:2015 Quality Management System, including participation in Internal Quality Audits (IQA), preparation of Corrective Action Reports (CAR), process documentation, and contribution to Management Review activities.
  • Serve as the liaison between regulatory authorities and internal departments, responding to regulatory inquiries and ensuring timely communication of regulatory requirements to relevant stakeholders.
  • Provide regulatory guidance and technical support to internal teams and third-party distributors to ensure compliance with regulatory and company standards.
  • Develop and maintain departmental procedures, standards, and documentation to ensure efficient regulatory and quality processes.
  • Provide regulatory intelligence by monitoring regulatory developments, guidance updates, and enforcement trends, and translating these into actionable recommendations for internal and external stakeholders.
  • Coordinate with operations and cross-functional teams regarding technical product information and regulatory compliance requirements.
  • Support regional RA/QA in driving cross-functional regional strategic initiatives and shared services to strengthen regulatory compliance, quality system effectiveness, process harmonization, and overall operational excellence across Southeast Asia + Taiwan (SEAT) region.
  • Perform other duties related to regulatory affairs and quality assurance as required to support business and compliance objectives.

 

Compliance

 

  • Review of Ethical Marketing and Compliance Programs, ensuring alignment with the APACMed Code of Conduct, company policies, and applicable healthcare compliance regulations.
  • Drive risk management initiatives by identifying, assessing, and mitigating potential compliance risks related to commercial activities, third-party engagements, and operational processes.
  • Act as the primary liaison for legal and compliance documentation, including Distributor Agreements, Accreditations, and Third-Party Due Diligence, coordinating with internal stakeholders and regional/legal teams to ensure proper review and compliance.
  • Oversee third-party compliance management, including onboarding, due diligence reviews, and risk assessments for distributors, vendors, and business partners.
  • Conduct compliance orientation and training programs for third-party vendors and distributors, anti-corruption requirements, and company compliance policies.
  • Provide advisory support to internal teams on compliance matters related to marketing activities, sponsorships, engagements with healthcare professionals (HCPs), and external partnerships.

 

Your Talents

 

  • Must possess Bachelor's/College Degree in Pharmacy (Pharmacy/Pharmacology) or equivalent.
  • Licensed Pharmacist
  • Minimum 7 years' working experience in the Regulatory Affairs Medical Device industry; with at least 2 years of management experience.
  • Extensive knowledge of applicable local government regulations.
  • Strong understanding of ASEAN Medical Device Directive (AMDD) and EU Medical Device Regulation (MDR)
  • Good working knowledge of Good Distribution Practice (GDP) and ISO 9001; experience with audits, inspections, and QMS implementation is essential.
  • Ability to inform and educate managers and department heads on regulations and polices that require regulatory affairs compliance.
  • Excellent written and verbal communication skills.
  • Excellent analytical and problem-solving skills.
  • Excellent strategic planning skills.
  • Proficient with applicable database and compliance software.
  • Proficient with Microsoft Office Suite or required software.

Your Benefits

  • Leave Benefits (Vacation Leave, Sick Leave, Parental Leave, etc.)
  • Birthday Benefits
  • Transport Allowance (if applicable to role)
  • Accessibility to Public Transport
  • Flexible Work Arrangements
  • Group Health Insurances (with 2 additional dependents)
  • Wellness Programs and Activities
  • Professional Development Opportunities
  • Global Exposure & Business Travel Opportunities (if applicable to role)
  • All other statutory benefits

HR Contact


5295