Quality & Laboratory Supervisor

Quality & Laboratory Supervisor Our client is a world leading supplier of biosecurity & infection control products for the past 50 years. Their dedication to Innovation has been a driving force behind this success. With approx. 1,700 employees across 120 countries, they are committed to driving a significant health impact globally. They are saving lives by improving access to safe drinking water with innovative, cost-effective products. One of their main products is used to disinfect 30 billion litres of water annually. They are currently seeking a Quality & Lab Supervisor to join an established team that is based in their manufacturing facility in Wexford. This is a full-time permanent position. The ideal person shall have a minimum of a Degree in Science with 4-5 years GMP industry experience. Role/Responsibilities: Manage the Laboratory & QC function, including staff, procedures, equipment, supplies and compliance with H&S, environmental (Green lab certification) and regulatory approvals. Assist with implementation of ISO, HPRA , FDA and other Customer or regulatory approvals. Lead and assist with GMP across the site. Co-ordinate the sampling and testing of raw materials, printed packaging, bulk intermediate and finished products, line clearances and on-line assessments. Facilitate the release of product. Liaise with production to ensure effective testing and release to meet production schedules. Actively participate in production problem solving and investigations as requested by supporting effective root cause analysis and timely closure of investigations. Ensure deviations & CAPAS are raised and brought to the attention of the relevant personnel. Be a change agent within the QC department by facilitating and leading appropriate change projects. Provide technical support to the Technical and Production teams as required. Ensure that all analytical methods and instruments are qualified/validated and calibrated according to the validation master plan and calibration schedule. Ensure documentation such as protocols, reports, SOP, STM etc are produced, reviewed, approved or updated according to validation requirements. Ensure accurate, up to date documented procedures are available and utilised within laboratory and associate functions. Ensure compliance to GLP and GMP within the laboratory. Liaise with Suppliers, where necessary, in relation to any issues relating to the quality of supplies. Carry out internal and external audits. Drive Quality Improvement projects and identify areas of opportunity for business improvement. Lead continuous improvement culture within the QC Team and the wider Company. Work closely with other members of the Technical Department to achieve the key technical objectives and overall key site objectives. Ensure all laboratory supplies (chemicals, hardware, glassware, and consumables) are purchased, safely stored, and stocks maintained at a level which supports all testing requirements. Be cost focused and support budget within area. Drive and promote the maintenance of good housekeeping, wellbeing and sustainability. Maintain and foster harmonious relationships with all members of staff. Education/Experience: Proven track record with supervisory experience in direct people management within the industry Scientific qualification (Degree) in life science discipline Knowledge of laboratory GMP standards Ability to articulate clearly when dealing with external bodies Ability to use sound judgment to make effective decisions within appropriate timeframes Proven to be self-directed, self-motivated and ability to priorities competing priorities The ideal candidate will be a self-starter with the ability to work on their own initiative and within teams Excellent ability to deliver results, with strong interpersonal, communication and influencing skills For further details please contact: Karen Shiel on or send CV to in confidence. Skills: Lab Management QC GMP