Team Lead Production

Description

• Shift Management & Oversight: Lead shift operations, including manpower allocation, production scheduling, and supervising the achievement of daily production targets.
• GMP & Quality Supervision: Monitor all onsite processes to ensure strict adherence to SOPs and GMP regulations; support the review and approval of Batch Records
• Troubleshooting & Issue Resolution: Provide immediate corrective actions and root cause analysis for technical issues or equipment failures occurring during production.
• Talent Development & Mentorship: Manage On-the-Job Training (OJT), technical guidance, and competency evaluations for new hires and junior operators.
• EHS (Environment, Health, and Safety) Leadership: Supervise safety protocol compliance within the shift, lead Near Miss reporting, and proactively identify/eliminate workplace hazards.
• Cross-functional Collaboration: Communicate effectively with Logistics, Quality (QA/QC), and Engineering departments to optimize production planning.
• Continuous Improvement (CI): Analyze shop-floor data to eliminate waste, improve production yields, and implement cost reduction initiatives.

Qualifications

Highest qualification: University

• Education: High school diploma or equivalent (Associate degree or higher in a related field preferred).
• Experience: Minimum 10 years of experience in pharmaceutical, biotech, or related manufacturing environments.
• Leadership: At least 3–5 years of experience in a leadership or supervisory role (e.g., Team Lead or Supervisor).
• Technical Skills: Deep understanding of GMP environments and high proficiency in process management and equipment operation.
  
  
• Experience in Single-use bioprocessing and Clean Room operations.
• Experience with Deviation management and CAPA (Corrective and Preventive Action) processes.
• Proficiency in ERP (SAP, etc.) and MES (Manufacturing Execution Systems).
• Basic English communication skills (ability to understand global guidelines, etc.).