Regulatory Affairs Manager at Dana Group

Job Responsibilities

• Interaction and co-ordination with pharmacy practice and regulatory bodies/agencies(SON,NAFDAC,PCN etc).
• Ensuring that regulatory requirement are complied with to the satisfaction of the relevant agencies.
• Guiding company to comply with regulatory requirements.
• Furnishing the Management with professional/technical information when required.
• Participating in advocacy and public corporate responsibility programs.
• Establishment and maintenance of cordial relationship with stakeholders in our business.
• Respond appropriately to any system failure or concerns that may arise.
• Make sure clear lines of accountability exist and that retrievable audit trails for documentations relating to operation of the company are kept.
• Make sure all professional activities undertaken by you or under your control are covered by adequate professional indemnity cover.
• Declare to the relevant person or authority any interest that could be perceived to influence your judgment which may impact on your regulatory activities.
• Development and registration of imported formulations and other pharmaceutical products.
• Regular warehouse inspection.
• Coordination of import of finished formulations, active pharmaceutical ingredients (APIs) and other medical/pharmaceutical products.
• Registration of premises of DPHL for distribution and wholesale when required.
• Registration/Renewal of DDL & DPHL products.
• Handling of compliance issue relating to the import and registration of imported products.
• Any other regulatory activities or roles assigned by the superior.

Job Requirements

• Candidates should possess a Bachelor's Degree qualification
• A minimum of 5 years work experience.