Quality Engineer at Katalyst Healthcares Life Sciences
Carlsbad, CA 92008, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

0.0

Posted On

13 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Management Skills, Working Experience, Microsoft Applications, Communication Skills, Analytical Skills

Industry

Other Industry

Description

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.
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
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