Production Team Leader

Location: North West / North Wales Salary: £43,000 - £47,000 Duration: 18 month FTC Overview An established pharmaceutical manufacturing organisation is seeking a Production Team Leader to support manufacturing operations within a regulated GMP environment. This position is responsible for leading a production team to ensure safe, compliant, and efficient manufacturing activities while driving operational performance and continuous improvement initiatives. The successful candidate will work cross-functionally with departments including Engineering, Quality, and EHS to ensure production targets, quality standards, and site objectives are achieved. Key Responsibilities Leadership & Team Management * Lead and support a manufacturing team to achieve operational targets and maintain high performance standards. * Conduct regular performance reviews, coaching, and development activities. * Identify training needs and ensure all team members are appropriately trained for assigned activities. * Promote a positive team culture focused on accountability, collaboration, and continuous improvement * Support effective communication across departments to resolve operational issues and improve processes. Production Operations * Ensure manufacturing activities are completed safely, efficiently, and in line with production schedules. * Monitor production performance and support delivery against KPIs including Right First Time (RFT). * Ensure production documentation is completed accurately and in compliance with GMP requirements. * Support deviation investigations, root cause analysis, and implementation of corrective actions. * Work closely with Engineering and support functions to coordinate maintenance, calibration, and validation activities. * Drive continuous improvement initiatives to enhance efficiency, quality, and operational performance. Quality & Compliance * Ensure all activities are performed in accordance with GMP and site quality standards. * Support inspection readiness and compliance with regulatory requirements. * Maintain accurate documentation including SOPs, batch records, and training records. * Promote a strong safety culture and ensure compliance with Environmental Health & Safety procedures. * Participate in audits, self-inspections, and quality improvement activities. Skills & Experience Essential * Experience working within a GMP-regulated pharmaceutical manufacturing environment. * Previous leadership or supervisory experience within manufacturing or operations. * Strong understanding of GMP documentation and compliance standards. * Excellent communication, organisational, and problem-solving skills. * Ability to work cross-functionally in a fast-paced manufacturing environment. Desirable * Experience within aseptic or sterile manufacturing environments. * Knowledge of continuous improvement methodologies such as Lean or Six Sigma. * Familiarity with electronic systems and manufacturing planning tools. * Scientific or engineering qualification, or equivalent industry experience. Personal Attributes * Strong leadership and people management capability. * Proactive and adaptable approach to changing business needs. * Detail-oriented with a strong focus on quality and compliance. * Analytical mindset with effective problem-solving abilities. * Team-oriented with a collaborative working style