QC Team Leader

Medifox DAN GmbH

Tebrau

Presencial

MYR 78.000 - 123.000

Jornada completa

14 días+

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Descripción de la vacante

Worklane GmbH in Malaysia is seeking a Manufacturing Quality Team Leader to drive GMP‑compliant quality control across goods in, in‑process and final production. You will lead a QC team, implement process controls and mentor staff.

The ideal candidate has at least 2 years in volume manufacturing, a tertiary science or engineering degree, and strong knowledge of GMP, FDA QSR and ISO standards. Experience managing people is preferred.

Formación

  • The candidate holds a tertiary qualification in Engineering or Science.
  • Minimum of 2 years industrial experience in volume manufacturing.
  • Solid knowledge of FDA QSR, GMP and ISO standards.

Responsabilidades

  • Lead, motivate, and support QC Inspectors to meet daily goals.
  • Oversee incoming, in‑process, and final QC checks and reporting.
  • Maintain records, investigate nonconformities, and drive CAPA.
  • Ensure GMP, 5S, and quality standards on the production floor.
  • Collaborate with cross‑functional teams and drive continuous improvement.

Conocimientos

Leadership
Communication
Cross‑functional collaboration
Problem solving
Attention to detail
Analytical thinking
MS Office / Oracle tools

Educación

Engineering or Science degree

Herramientas

Microsoft
Oracle

Descripción del empleo

Job Description

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 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.

Key Responsibilities
Team Leadership
  • 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.
QC Inspection & Reporting
  • 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.
Safety
  • Support rehabilitation of injured employees and uphold Duty of Care obligations.
  • Promote safe work practices and prevent OH&S hazards, especially around manual handling.
GMP & Housekeeping
  • Ensure GMP, 5S, and quality standards are consistently followed on the production floor.
Qualifications & Experience
Core Competencies
  • 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.
Required
  • 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.
Preferred
  • Experience managing people or leadig teams.

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you,

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