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Site Lead

2 months ago


Newry Co Down, United Kingdom Next Phase Recruitment Full time
About the Role

We are seeking an experienced Operations Site Lead to join our team at Next Phase Recruitment. As a key member of our manufacturing team, you will be responsible for leading high-performing teams in the production of veterinary pharmaceutical products to the highest standards.

Key Responsibilities
  • Develop and lead high-performing teams in one of our manufacturing sites in Northern Ireland.
  • Drive a safety culture and maintain the highest level of safety standards.
  • Embed continuous improvement and a quality mindset within the team.
  • Embed an effective two-way communication culture on site, ensuring business updates are frequently communicated and queries are dealt with in a timely manner.
  • Coach and mentor team members to drive high standards of performance.
  • Responsibility for ensuring customer requirements are exceeded, through effective coordination and planning of the manufacturing schedule.
  • Identify process improvements to maximize output and efficiency of the facility.
  • Partner with other site leads to ensure change is implemented consistently across sites, avoiding any silo mentality.
  • Responsibility for operational and compliance KPIs for manufacturing facilities on site.
  • Ensure products are manufactured to the highest standards and associated records are completed compliantly at all times.
  • Liaise with and promote teamwork with other departments such as engineering, process excellence, validations, and quality to ensure all production equipment and areas are fully compliant with all GMP and customer requirements.
  • Lead the change management process for manufacturing issues.
  • Actively engage in continuous improvement programs ensuring that all manufacturing activities are carried out in the most cost-effective manner, minimizing reject levels and maximizing yields to ensure that daily production targets and annual departmental goals are met.
  • Adhere to the principles of Good Manufacturing Practice ensuring product is manufactured within the defined parameters of the Quality Management System. Where deviations occur, suggest and implement CAPAs. Lead investigations and suggest CAPAs for manufacturing issues.
  • Perform regular internal compliance audits against the appropriate regulations to ensure an audit-ready production facility. Assist with external audits as required.
  • Drive high standards of performance within the team and identify development needs/skills gaps.
Requirements
  • A degree or third-level qualification in pharmacy, science, engineering, or mathematics (or a closely related area) or at least 5 years' experience in a manufacturing environment in the pharmaceutical industry.
  • A minimum of 7 years' experience in a management role, directly managing managers who individually manage teams.
  • Experience and understanding of pharmaceutical manufacturing, regulatory, quality, and validation requirements, pharmaceutical manufacturing processes (e.g., solid oral dose, aseptic, non-aseptic techniques, API manufacturing, and packaging, including materials, sciences, and technology activities) and product launch.
  • Ability to think strategically and act tactically, comfortable with getting into the detail as required.
  • Demonstrated ability to maintain a compliant and safe working environment, delivering products at high quality and in line with regulatory standards.
  • Excellent leadership skills with demonstrable ability to motivate and train team members; coach new/less experienced team members.
  • Experience of environmental, health, and safety (e.g., complete risk assessments, COSHH assessments, NEBOSH).
  • Knowledge of control of documents (including a document management system).
  • Experience of documentation associated with a Quality Management System.
  • Understanding of production documentation processes.
  • Excellent IT skills (PowerPoint, Excel, Word).
  • Excellent organizational and communication skills with ability to successfully implement change.
Desirable Criteria
  • Experience in aseptic manufacturing.
  • Experience of inventory control systems.
  • Experience of control of cross-contamination (microbial or chemical).