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Quality Control Manager - Medical Device Garments

MAS Holdings · Colombo

New
Senior 🇬🇧 English
ISO 13485 GLP/GMP ISO 14971 Six Sigma Lean manufacturing CAPA Change control Root cause analysis

Job description

About the role

The Wearables and Growth Platforms team is building, scaling and commercialising wearable technology and medical device businesses. It is looking for a Quality Control Manager in Colombo to lead quality across the development and manufacture of soft goods for medical device garments, ensuring compliance with global regulatory standards.

Key responsibilities

  • Establish, implement and maintain quality system processes aligned with ISO 13485 and GLP/GMP across product development and manufacturing.
  • Ensure ongoing compliance with ISO 14971 (risk management) and regional regulations such as US FDA, EU MDR and TGA.
  • Own regulatory audit readiness and act as a key contact during external and internal audits.
  • Lead quality risk management across the product lifecycle, from design through manufacturing.
  • Develop, implement and maintain quality control plans, including documentation review and approval processes.
  • Design, verify and validate quality control test methodologies for soft goods and textile-based medical device garments.
  • Drive quality involvement in new product integration and lead design transfer planning from development to manufacturing.
  • Manage supplier quality and act as the primary quality liaison with contract manufacturers.
  • Lead root cause analysis for quality issues and non-conformances, manage change control and CAPA, and set up ongoing monitoring and control mechanisms.
  • Lead, manage and motivate a cross-functional quality team and report progress to leadership.

Required profile

  • BEng, BSc, BTec or equivalent technical degree with a minor in management studies.
  • Solid background in materials, textiles or garment development, manufacturing and quality control/testing.
  • Proven people management experience leading teams in a technical or manufacturing setting.
  • Hands-on experience implementing GLP/GMP and ISO 13485, ideally in medical devices or healthcare products.
  • Track record managing supplier quality programs and contract manufacturer relationships.

Required skills

  • Quality risk management, QC planning and execution, and documentation control.
  • Experience developing and validating QC test methods.
  • Root cause analysis, CAPA and change control.
  • Building and reporting quality metrics to senior leadership.
  • Added advantage: CQE/CQA, Lean manufacturing, Six Sigma green/black belt, GMP/ISO auditor.

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Published 1 hour ago

Expires 1 month from now

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MAS Holdings

Colombo