Kelsius

Operations Manager

Quality Manager

•	Maintaining the Quality & Environmental System in line with ISO90001 & ISO14001 standards
•	Supporting external audits by regulatory agencies and customers
•	Complete Internal Audit identifying gaps and areas for improvement. Following implementation of audit actions ensure effectiveness and compliance.
•	Raising non-conformity and corrective action reports, completing root cause analysis, completing risk assessments and issuing corrective actions
•	Working with the Quality and Environmental Management Team to ensure Objectives for continuous improvement (based on the strategic direction of the company) have been met.
•	Use of Salesforce and Excel to generate weekly manufacturing build schedules
•	Purchasing and control of stock to support manufacturing
•	Working with Customer Services, Sales and Dispatch to ensure Customer timelines are met
•	Management of Quality Assurance, Stock Control and Dispatch staff
•	Relationship building with Suppliers and Couriers

Quality Assurance and Stock Control Manager

Randox Life Sciences

Manager of the Biochip Manufacture and Quality Control of Biochip and Randox Machines
•	Ensuring manufactured product met specification
•	Investigation of Non-conforming Products and completion of Corrective Actions Reports
•	Maintaining Quality Standards 
•	Supporting ISO13485 and FDA audits
•	Ensuring equipment and clean rooms were maintained to a high standard, and calibrated or validated
•	Training and mentoring of staff
•	Creation and revision of Standard Operating Procedures and Work Instructions

Biochip Formulation Manager

Almac Group

•	Quality Control supporting large scale API Manufacture, including testing of raw materials, in process Controls, isolated intermediates and APIs.
•	Generation of Certificates of Analysis
•	Raising Out of Spec investigations. Participation in root cause investigations and implementation of corrective actions
•	Internal audit Walk-through
•	Scheduling and prioritising workloads for shift analysts
•	Training analysts on procedures, methods and equipment
•	Accurate record keeping and report writing.
•	Responsible for Lab preparation prior to customer audits, MHRA, FDA audits

Technical Leader

Reliable, dynamic and highly motivated individual, with solid experience in the manufacturing industry. Highly competent in stock control and production planning and all aspect of quality management. Energetic and enthusiastic with the capacity to engage and communicate effectively with others.

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