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.

• 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