Stuart Mcculloch Email & Phone Number

Girvan Distillery

To ensure that the Girvan Site is fully compliant with all relevant current and future legislation in the areas of Health & Safety and the Environment.

Dalry, Ayrshire

Championing manufacturing excellence in Final Product processing and packing areas. Communicating the quality standards required by cGMP including the coaching and training of personnel on quality, cGMP and hygiene standards. Leading quality investigations and reporting process including quality deviation investigation and customer compliant investigation processes in accordance with QMS. Providing pragmatic and supportive problem solving and decision making in relation to quality related… Show more Championing manufacturing excellence in Final Product processing and packing areas. Communicating the quality standards required by cGMP including the coaching and training of personnel on quality, cGMP and hygiene standards. Leading quality investigations and reporting process including quality deviation investigation and customer compliant investigation processes in accordance with QMS. Providing pragmatic and supportive problem solving and decision making in relation to quality related issues. Lead auditor for external and internal QMS audits against ICHQ7, EU GMP Part 2, ISO9001, ISO14001 and FSSC 22000 regulatory requirements. Show less

Provided consultation services in relation to the decommissioning and dismantling of API pharmaceutical plant.

Irvine, Ayrshire

Responsible for providing technical and cGMP support to the manufacture of intermediate and final API products within designated areas of manufacturing to ensure compliance with ISO9001 and ICH Q7A. Provide improvements and troubleshooting support to manufacturing processes to ensure quality, increased yield and throughput using Lean Six Sigma techniques and continuous improvement methodology. Deviation and failure investigation (CAPA) and root cause analysis reporting. Control and management… Show more Responsible for providing technical and cGMP support to the manufacture of intermediate and final API products within designated areas of manufacturing to ensure compliance with ISO9001 and ICH Q7A. Provide improvements and troubleshooting support to manufacturing processes to ensure quality, increased yield and throughput using Lean Six Sigma techniques and continuous improvement methodology. Deviation and failure investigation (CAPA) and root cause analysis reporting. Control and management of change using QMS. Show less

Cupar, Fife

Contract Research Organisation specialising in quality custom synthesis and process development for clients in the pharmaceutical industry. Responsible for all cGMP production associated aspects – compliance and validation of processes and systems, preparation and review of batch documentation, health and safety, production planning and plant operations. Preparation and review of technical and quality reports for clients.

Montrose, Angus

Project manager for manufacturing campaigns. Responsible for all relevant documentation, planning, operator training; ongoing adherence to the manufacturing plan; dealing with technical issues. Process champion for processes under direct supervision. Responsible for maximising quality, yield and throughput as well as contributing to process development projects. Proactively managed all internal manufacturing improvement activities for the area of responsibility to meet/exceed the requirements… Show more Project manager for manufacturing campaigns. Responsible for all relevant documentation, planning, operator training; ongoing adherence to the manufacturing plan; dealing with technical issues. Process champion for processes under direct supervision. Responsible for maximising quality, yield and throughput as well as contributing to process development projects. Proactively managed all internal manufacturing improvement activities for the area of responsibility to meet/exceed the requirements of business management and customers. Show less

Montrose, Angus

Responsible for the day-to-day operation and management of the laboratory and personnel to ensure the analytical analysis of site effluent complies with GLP/GMP and discharge consent (SEPA).

Montrose, Angus

Process development and troubleshooting support to the manufacture of established products and new chemical entities in order to achieve compliant, cost effective and secure supply. Process Contact and Shift Chemist responsible for the technical support to manufacturing operations. Supervision of laboratory technicians in managing their weekly activities.

Loughborough, Leicestershire

Produced quantities of designated compounds, in high purity, for clinical evaluation and safety studies and investigated and developed practicable syntheses to these compounds.

Pgdip, Safety & Risk Management

Phd, Synthetic Organic Chemistry

Thesis, “Tandem Radical Macrocyclisation-Transannulation Reactions Towards Steroid Construction”, carried out under the supervision.

Chemistry With Medicinal Chemistry, First Class Honours

Honours thesis carried out under the supervision of Professor G.W. Kirby, FRS. The synthesis of an aryl adamantyl guanidine for use.