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Site Lead

2 months ago

Newry, 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 operations team, you will be responsible for leading high-performing teams in our manufacturing facilities, ensuring the highest standards of quality and safety are maintained.

Key Responsibilities
  • Develop and lead high-performing teams in our manufacturing facilities, driving performance and embedding a continuous improvement culture.
  • Drive a safety culture and maintain the highest level of safety standards, ensuring compliance with regulatory requirements.
  • 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 and ensure customer requirements are exceeded.
  • Identify process improvements to maximize output and efficiency of the facility, partnering with other site leads to ensure consistent implementation.
  • Ensure products are manufactured to the highest standards, associated records are completed compliantly, and Operational and Compliance KPIs are met.
  • Liaise with and promote teamwork with other departments 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 engaging in continuous improvement programs to minimize reject levels and maximize yields.
  • Adhere to the principles of Good Manufacturing Practice, performing regular internal compliance audits and assisting with external audits as required.
Requirements
  • A degree or third-level qualification in Pharmacy, Science, Engineering, or Mathematics, 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, 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 or less experienced team members.
  • Experience of environmental, health, and safety, including risk assessments, COSHH assessments, and 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, including PowerPoint, Excel, and Word.
  • Excellent organizational and communication skills, with the ability to successfully implement change.