The Role:The Production Supervisor will oversee manufacturing operations in a manufacturing environment, ensuring efficient production, compliance with regulatory standards, and adherence to quality and safety protocols. The role involves leading a team, optimizing workflows, and driving continuous improvement initiatives.Key Responsibilities:Supervise daily production activities to meet output, quality, and efficiency targets.Ensure compliance with medical device regulations (FDA, ISO 13485, GMP).Train, mentor, and manage production staff to enhance team performance.Monitor and enforce safety protocols to maintain a safe working environment.Collaborate with engineering, quality, and supply chain teams to resolve production issues.Implement lean manufacturing and continuous improvement initiatives.Maintain accurate documentation and reporting for audits and compliance.Troubleshoot and resolve equipment or process inefficiencies.Support new product introductions and scale-up manufacturing processes.Required Qualifications & Skills:Bachelor's degree in Engineering, Manufacturing, or related field, or equivalent experience.3 years of supervisory experience in a medical device or regulated manufacturing environment.Strong knowledge of GMP, FDA regulations, and ISO 13485 requirements.Excellent leadership and team management skills.Experience with lean manufacturing and process optimization.Strong problem-solving and decision-making abilities.Effective communication and interpersonal skills.Preferred Qualifications:Six Sigma or Lean Manufacturing certification.Experience with ERP/MES systems in a manufacturing setting.Familiarity with validation and process improvement methodologies.For a confidential conversation about the role please apply for the role or contact Owen Clancy at By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose.