About the Role
The QCR will implement inspection and test plans for each project. They will maintain and distribute accurate drawings and red line corrections throughout fabrication process, maintain quality control records, documents and logs.
Quality Control Representitive Tasks:
Updating and maintaining current ISO paperwork including:
Standard operating procedures (SOPS)
QC check lists
Change to documentation log
Corrective and preventive action report log (CPAR)
Maintenance records for equipment
Confirm that the latest revisions are accurate and being implemented as expected.
Be responsible for internal audits annually
Audit each area for:
Weak points in the process. Highlight potential failure nodes in the systems.
Highlight areas for improvement, recommend resolutions and document the advantages of the changes.
Cover all areas required by ISO
External audits annually from Medical clients
Evaluate any recommendations and their implication on quality and productivity
Respond to non-conformances, if any.
Respond and liaise with clients on resolutions on the above.
Chair the management review meetings annually
Implement resolutions to CPAR reoccurances.
Examine recommendations and their implications on quality and productivity.
Cover all areas required by ISO.
About the Company