Documentation Officer

Global Organics Limited | Lagos, Nigeria

Full-Time Posted today 3 views

About the Role

Global Organics Limited has been a pioneer in launching pharmaceutical drugs, such as Paragol, first in Nigeria. Evolving from a trusted importer, our vision now focuses on expanding operations into local manufacturing of both human pharmaceuticals and veterinary drugs. We are seeking a highly organized, detail-oriented, and responsible Documentation Officer to join our dynamic team and support our continued growth and regulatory excellence.

Key Responsibilities
  • Assist in the compilation, review, maintenance, and updating of Common Technical Document (CTD) dossiers.
  • Gather, organize, file, and archive addendum and supporting documents for regulatory submissions.
  • Monitor, track, and upload regulatory information on relevant platforms including NAPAMS, DMS, and GS1.
  • Maintain proper records relating to Adverse Drug Reactions (ADRs) and pharmacovigilance activities.
  • Track submission deadlines, product renewals, variations, and follow up on outstanding documentation.
  • Ensure the integrity, confidentiality, traceability, and accessibility of all regulatory documents.
  • Liaise with Regulatory Affairs, Quality Assurance, Production, and other departments to obtain required files.
  • Support internal and regulatory audits by promptly retrieving and presenting required documentation.
Qualifications
  • Bachelor Degree in Pharmacy, Pharmacology, Biology, Epidemiology, Biological Sciences, or related fields.
  • Minimum of 2 years of relevant experience, preferably within a pharmaceutical manufacturing company.
  • Familiarity with CTD dossier compilation, NAPAMS, DMS, and GS1 platforms is a strong advantage.
  • Proficiency in Microsoft Office Suite, particularly Microsoft Word and Excel.
  • Strong documentation, organizational, analytical, and record-keeping skills.
  • Excellent attention to detail and ability to maintain accuracy under pressure.
  • Good written and verbal communication skills.
Benefits
  • Competitive salary and performance-based incentives.
  • Opportunities for professional growth in pharmaceutical manufacturing.
  • Comprehensive health insurance and medical benefits.
  • Collaborative and innovative work environment.

Skills

Documentation Regulatory Affairs CTD Dossiers NAPAMS Pharmacovigilance GMP Compliance Record Keeping Microsoft Excel
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