Senior Regulatory Affairs Strategist - MedTech Submissions

Antler; Taguig; On-site; PHP 600,000 - 950,000; Full time

Job summary

Johnson & Johnson in Taguig, Philippines, seeks a Senior Regulatory Affairs Specialist to ensure regulatory compliance of medical devices and to input into global regulatory strategy. You will identify local requirements for filings and support line extensions and new product introductions.

The role requires active pharmacist licensure in the Philippines, strong attention to detail, and experience with local health authority submissions in a fast-paced environment.

Qualifications

• Bachelor's degree in pharmacy with active pharmacist license in the Philippines.
• Familiarity with medical device regulatory systems and product registration requirements in the market.
• Experience with the local health authority for regulatory activities.

Responsibilities

• Prepare submissions to local health authority for new products and variations.
• Maintain regulatory approvals databases.
• Review labelling and promotional materials as required.
• Coordinate with regulatory colleagues to gather documents for registrations.
• Engage with HA and industry groups on regulatory developments.
• Support audits and improvement of regulatory processes.

Skills

Regulatory submissions

Analytical skills

Attention to detail

English proficiency

Team player

Regulatory knowledge

Problem solving

Communication

Education

Bachelor's degree in Pharmacy

Job description

Johnson & Johnson in Taguig, Philippines, seeks a Senior Regulatory Affairs Specialist to ensure regulatory compliance of medical devices and to input into global regulatory strategy. You will identify local requirements for filings and support line extensions and new product introductions.

The role requires active pharmacist licensure in the Philippines, strong attention to detail, and experience with local health authority submissions in a fast-paced environment.