On-site Regulatory Affairs Pharmacist — FDA Submissions

Sanimed Pharmaceuticals Inc.; Philippines; On-site; PHP 360,000 - 720,000; Full time

Job summary

Sanimed Pharmaceuticals Inc. in Makati, on-site, seeks a Regulatory Affairs professional with 1-3 years of experience and a Bachelor’s degree in Pharmacy or related field.

You will ensure compliance with Philippine FDA regulations, prepare regulatory documents for drug registration, review labeling and packaging, and communicate with agencies. The role emphasizes meticulous documentation, cross-functional teamwork, and staying current with evolving guidelines to support product approvals and

Qualifications

• Bachelor’s degree in Pharmacy or related field.
• 1–3 years of experience in regulatory affairs or related field.
• Strong understanding of regulatory guidelines and processes.
• Detail-oriented with excellent organizational skills.
• Ability to work effectively in a team environment.
• Ability to manage multiple projects and meet deadlines.

Responsibilities

• Ensure compliance with regulatory requirements in pharmaceutical product development.
• Prepare and submit regulatory documents for drug registration and marketing.
• Review and evaluate labeling, packaging, and advertising materials for compliance.
• Communicate with regulatory agencies regarding product information and compliance issues.
• Conduct training sessions for internal teams on regulatory requirements and updates.
• Familiarity with product registration, labeling requirements and regulatory documentation.
• Up-to-date knowledge of relevant FDA regulations and guidelines.

Skills

Regulatory guidelines

Documentation skills

Analytical skills

Organizational skills

Communication skills

Education

Bachelor’s degree in Pharmacy

Job description

Sanimed Pharmaceuticals Inc. in Makati, on-site, seeks a Regulatory Affairs professional with 1-3 years of experience and a Bachelor’s degree in Pharmacy or related field.

You will ensure compliance with Philippine FDA regulations, prepare regulatory documents for drug registration, review labeling and packaging, and communicate with agencies. The role emphasizes meticulous documentation, cross-functional teamwork, and staying current with evolving guidelines to support product approvals and