TRAINING AND REGULATORY OFFICER (EXPERIENCE WORKING WITH PHARMACISTS AND PPB)

DUTIES AND RESPONSIBILITIES

Regulatory Affairs

• Prepare, compile, and submit dossiers to PPB for medicine registration.
• Liaise with PPB officials to ensure timely approvals and compliance.
• Manage product licensing and renewals.
• Maintain accurate regulatory documentation.
• Stay updated on changes in pharmaceutical legislation and regulatory guidelines.

Training

• Develop and deliver training programs for internal staff on compliance, regulatory updates, and product knowledge.
• Ensure all sales and medical teams are aware of legal and compliance requirements.

Compliance Support

• Ensure company operations meet local regulatory requirements.
• Support audits and inspections.

KEY REQUIREMENT SKILLS AND QUALIFICATION

• Degree in Pharmacy, Pharmaceutical Science, Biochemistry, or related Life Sciences field
• At least 3–5 years’ experience in a regulatory affairs or training role within a pharmaceutical company
• In-depth knowledge of PPB regulations, GMP/GDP guidelines, and pharmaceutical quality systems
• Proven experience preparing and submitting regulatory filings and handling audits/inspections
• Certification in Regulatory Affairs, Training & Development, or Quality Assurance will be an added advantage

HOW TO APPLY

• If you meet the above qualifications, skills and experience share CV on This email address is being protected from spambots. You need JavaScript enabled to view it.
• Interviews will be carried out on a rolling basis until the position is filled.

Only the shortlisted candidates will be contacted.