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The primary role of Manufacturing Quality function is to design, implement and monitoring quality control programs. Key deliverables include, but not limited to, recommending changes to methods, procedures and standards to improve quality of output based on analysis of data and systems. Ensures products are built correctly to specification, quality standards and appropriate regulatory compliance. Reports defects and tracks until resolution. The Quality Control Team Leader (Day Shift) is responsible for leading the QC team, ensuring compliance to quality systems, and supporting inspection activities across Goods Inwards, in‑process, and final production stages. The role emphasizes strong leadership, process control, continuous improvement, and adherence to GMP and safety standards.
Job Responsibility:
Lead, motivate, and support QC Inspectors to meet daily operational goals
Conduct training on procedures and product specifications
maintain LMS training records
Mentor team members, identify development opportunities, and coordinate skills improvement
Build strong working relationships with cross‑functional teams
Ability to lead and support global projects or continuous improvement projects
Support the calibration team in maintaining calibration systems and driving improvement
Oversee QC processes for incoming materials, in‑process checks, and outgoing checks
Resolve daily QC issues using sound problem‑solving techniques
Ensure records are properly maintained, filed, and archived without backlog
Manage nonconforming materials and drive timely investigations and dispositions
Improve QC processes and provide monthly KPI tracking, including SPC analysis
Support rehabilitation of injured employees and uphold Duty of Care obligations
Promote safe work practices and prevent OH&S hazards, especially around manual handling
Ensure GMP, 5S, and quality standards are consistently followed on the production floor
Requirements:
Tertiary qualification in Engineering or Science
Minimum 2 years of industrial experience, preferably in volume manufacturing
Solid knowledge of FDA QSR, GMP, and ISO standards
Strong understanding of GMP, quality systems, and regulatory requirements
Ability to maintain process documentation and ensure product traceability
Strong analytical capability for root cause and corrective action analysis
Effective communication, leadership, and cross‑functional collaboration
Able to manage multiple priorities with attention to detail
Proficient in Microsoft, Oracle, and relevant software tools