Execution of batch process as per batch processing record in Granulation, Compression and Coating, Packing. Execution of equipment operation & cleaning activities as per SOP
Effectively generate new business leads and opportunities from various sources and engage through proper prospecting, email campaigns, cold-calling and regular follow-ups
Seasoned experience in handling of various EU procedure like DCP, MRP, National. National phase handling for EU procedures.
Post approval variation compilation and filling to various EU agencies
Promptly notify and escalate to JAMP headquarters quality department any potential quality or regulatory issues that may affect product quality or regulatory compliance
Unique Pharmaceuticals Limited is a pioneer in the pharmaceutical industry in Nigeria. We have been serving the healthcare sector since 1988 through the production & distribution of quality pharmaceutical products, notably I.V. Fluids products manufactured using the innovative and High -Tech manufacturing process known as Form – Fill – Seal Technology.
Ensure preparation, review and submission of CTD sections in compliance with requirements of EMA, USFDA and other global markets. Timely update and preparation of dossier and documents as well as responses to the queries raised by regulatory agencies
Must have experience in the development of nasal spray, nebuliser and other respiratory dosage form. Exposure of regulated and domestic product development
Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia