Quality Engineer

Company : Katalyst Healthcares & Life Sciences

Responsibilities:

• Participate in Suppliers' and contract manufacturers' performance scorecards as required.
• Coordination and execution of QMS audits (Internal and Vendor) as required.
  
  Act as Quality representation for product innovation processes as directed by the Quality Director.
• Coordinate the calibration and preventive maintenance processes of the measurement devices in all client sites.
• Manage all Quality Management system activities including CAPA, Management Review, and Document Control.
• Conduct failure analysis on returned products.
• Support client WH and VAS centre regarding work instructions and process definition.
  
  Other duties as assigned.

Requirements:

• Minimum 5 years of working experience as a Quality Engineer in a manufacturing environment.
• Experience in ISO Quality Systems Implementation and Management.
• Bachelor's degree or equivalent work experience in a Manufacturing environment.
• Strong knowledge of MS Excel and skills in other Microsoft applications (i.e. Word, PPT, etc.)
• ISO Led auditor/Auditor certified preferred.
• ISO 9001 Quality System Managements.
• PPAP, FMEA, SPC, Lean-Six Sigma methodologies.
• Strong analytical skills to identify the source of problems and to propose solutions.
• Strong organizational and communication skills.
• Ability to multi-task and meet deadlines.
• Demonstrated time management skills.
• Strong attention to detail.
• Positive attitude, self-motivated and eager to succeed.

Apply Online