Senior Regulatory Affairs Specialist, MedTech – PH

Johnson & Johnson; Pateros; On-site; PHP 800,000 - 1,100,000; Full time

Job summary

Johnson & Johnson is seeking a Senior Regulatory Affairs Specialist for its MedTech regulatory affairs team in Taguig, Philippines. You will drive regulatory submissions, maintain approvals databases, and collaborate with cross-functional teams to ensure compliant product registrations and labeling.

You will engage with local health authorities, monitor regulatory changes, and support audits while contributing to continuous improvement of regulatory processes within the department.

Qualifications

• Bachelor’s degree in pharmacy with active pharmacist license registered in the Philippines.
• Familiarity with medical device regulatory systems and product registration requirements.
• Experience with local health authority submissions and registrations.
• Strong attention to detail and methodical data handling.
• Excellent verbal and written English communication; able to work in a matrixed environment.

Responsibilities

• Prepare regulatory submissions to the local health authority for new products and variations.
• Maintain departmental and source company databases of regulatory approvals.
• Review labeling and promotional materials as required.
• Coordinate with regulatory colleagues to gather documentation for registrations.
• Engage with HA and industry groups to stay current on regulatory changes.
• Support audits and drive continuous process improvements.

Skills

Analytical reasoning

Regulatory affairs

Communication

Documentation

Teamwork

Problem solving

Education

Bachelor's degree in Pharmacy with active pharmacist license (Philippines)

Job description

Johnson & Johnson is seeking a Senior Regulatory Affairs Specialist for its MedTech regulatory affairs team in Taguig, Philippines. You will drive regulatory submissions, maintain approvals databases, and collaborate with cross-functional teams to ensure compliant product registrations and labeling.

You will engage with local health authorities, monitor regulatory changes, and support audits while contributing to continuous improvement of regulatory processes within the department.