This person will be responsible for the corrective action process, the internal audit process, and the document control process.
Responsibilities:
· Maintain and revise Quality Management System (QMS) procedures and work instructions as necessary to comply with ISO 9001:2015 and AS9100D standards.
· Facilitate review and disposition of updates to Quality Management System procedures and work instructions.
· Train process owners of the QMS procedures and work instructions on the proper content and level of detail in each type of document to ensure consistency across the QMS.
· Create, coordinate, and facilitate all internally issued corrective actions with assignees.
· Assist manufacturing, quality, and engineering teams in determining effective corrective actions.
· Verify completed corrective actions are effective in preventing the reoccurrence of the original problem and root causes.
· Track status and issue monthly metrics for internal and external corrective actions for review by the management team.
Desired Skills and Qualifications:
· Experience working in a manufacturing company with ISO9001:2015 and AS9100D accreditation.
· Experience performing root cause analysis using 5-Why, 8D Problem Solving, or Fishbone Diagram methods.
· Experience with QMS audits performed by customers and external auditors.
· Experience with QMS internal audits.
· Excellent English written and oral communication skills.
· Action-oriented and resilient, staying composed and focused under stress. Comfortable with ambiguity and change.
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