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Fidson Healthcare Plc is a leading pharmaceutical manufacturing company in Nigeria. Founded in 1995, we have relentlessly pursued our goal of becoming a leading player in the pharmaceutical landscape in Nigeria. Ever since, we have built and cultured an organizational framework that has steadily helped us gain ascendancy in the industry. We have crafted the pharmaceutical architecture of the industry over the years of our existence, playing very defining roles in the emergence of the new generation of industry players. Innovation, Excellence, Passion, Integrity and Ownership...are five core values that form the substructure on which we have built a world-class company that has earned the respect and admiration of even the fiercest of our competitors.
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Location: Factory- Ota, Ogun State Department: Quality & Regulatory Affairs Does The Cap Fit?
We seek proactive and innovative individuals who can think on their feet and deliver excellent results consistently. Our ideal candidates are organised, meticulous, self-driven, receptive to learning, team-spirited and can sustain the passion to make an effective impact in a fast-paced work environment.
Effectively manages all controlled documents such as Batch Records, SOPs, Specification Documents, Test Protocols, Validation Documents etc. to prevent unauthorized access, use, disposal, etc.
Ensures traceability of all quality documentation (e.g, batch documents, certificates of analysis, etc.) through effective storage and retrieval system.
Manages documentation process to ensure that all deviations/ investigations/ change control, incidents are duly documented, completed, communicated, approved and appropriately filed.
Conduct Periodic Product Quality Review in order to determine the current quality profile of the products and promote their continuous improvement.
Provides all necessary technical information required for on-time registration of existing and new products by NAFDAC and other relevant regulatory bodies
Organises effective destruction of operational document/ quality records at the end of its expiry life i.e. annual destruction of MBS & PBS.
Monitor compliance with the Regulatory Procedures SOPs and ensure that they are updated regularly as required.
To ensure all Manufacturing/Packaging Batch Product documents are duly signed by respective authorities.
To effectively carry out validation and qualification of equipment and processes.
Prepares a weekly report on all activities on the job.
To assist in any other areas of work within the section as appropriate.
First Degree in Chemistry (Bio/Pure/Applied/Industrial), Microbiology and other related science courses.
Required Years of Experience: 2-4 Years
Method of Application
Interested and qualified candidates should Click Here to Complete "Application Form" and then Click Here to submit "Curriculum Vitae (CV)".
Note: Complete the Application Form before uploading your Curriculum Vitae. You can only apply for one (1) role