Job Summary
The development and implementation of efficient laboratory policies, along with skilled administration and management, are essential responsibilities.
Develop and maintain a comprehensive Documentation Management System to streamline operational processes. Ensure accurate, accessible, and up-to-date documentation for all critical operational activities.
Investigates and addresses deviations and non-compliance observations to ensure adherence to regulatory standards and internal policies.
To ensure strict adherence to Good Manufacturing Practices (GMP) standards, the role involves establishing, implementing, and rigorously enforcing GMP principles across all production processes.
Oversee compliance with NAFDAC GMP standards within an approved manufacturing facility, as outlined in the attached floor plan upon request.
Weekly production planning involves establishing and organizing manufacturing schedules to meet demand forecasts and operational objectives. This process includes assessing resource availability, coordinating with various departments, and ensuring that production targets are met efficiently and on schedule. Additionally, it requires monitoring progress, adjusting plans as necessary, and reporting performance metrics to stakeholders to maintain alignment with business goals.
Inventory management involves overseeing and maintaining accurate records for concentrates, packaging materials, and related supplies to ensure optimal availability and efficient tracking throughout the supply chain.
Conduct research and development activities to drive innovation and enhance product offerings.
Overseeing production and operational workflows and protocols ensures adherence to established standards and optimal performance. This role involves monitoring and managing processes to maintain efficiency, quality, and compliance with organizational guidelines. Responsibilities include evaluating workflows, identifying areas for improvement, and implementing corrective actions as necessary to enhance productivity and meet operational objectives.
Process and method validation activities encompass a comprehensive evaluation to confirm that procedures, processes, and systems consistently produce results meeting predetermined specifications. This involves meticulous documentation, rigorous testing phases, and detailed analysis to ensure compliance with regulatory standards and operational requirements. Validation efforts typically include installation qualification (IQ), operational qualification (OF), and performance qualification (PQ) to systematically verify equipment, processes, and methods function as intended under intended conditions. Strong attention to detail, adherence to protocols, and a methodical approach are essential to achieve accurate and reproducible outcomes.
The production staff will undergo comprehensive GMP and safety training, encompassing both structured educational sessions and hands-on practical exercises to reinforce learning and ensure full compliance with industry standards.
Facilitates productive engagement with essential stakeholders to ensure alignment and shared objectives throughout project execution.
Prospective applicants who meet the necessary qualifications are encouraged to submit their CV to oawolesi@animalcare-ng.com, ensuring the subject line includes “Quality Control.”
Qualifications
BA/BSc/HND
