DUTIES AND RESPONSIBILITIES- Document policies and procedures as requested by department heads or as part of corrective and preventive action to be taken.
Receives, reviews and route for approval the request for new forms or documents- Upload the new form or document in forms online/documents online.
Informs the department heads regarding the availability of the new form/s or document/s in the forms online/document online.
- Maintains and updates the master list of forms and documents.
Issues hardcopy of the new documents or forms to process owner.- Retrieves obsolete hard copies of documents and ensures that no obsolete documents are uploaded in the form/s or document/s online.
Conducts QMS audit base on approved quality plan and submit accomplished audit checklist to the Lead Auditor or / PIA Manager for verification.
- Facilitates Process Improvement Meeting as a result of audit / complaints monitoring.
Conducts investigation on incidents / complaints as instructed by PIA Manager.- Assist Officers and Managers in verifying existing policies and procedures.
Perform process improvement study as assigned. (e.g. capacity planning, facility layout, time study etc.)
- Performs other tasks from time to time.
Candidate must possess a Bachelor's / College Degree in Industrial Engineering / Manufacturing Management in Quality Management/ Industrial Quality Management or any Medical Course with graduate certificate course in quality management.
- Knowledgeable in ISO 9001 standards, documentation and audit.
Minimum of 1 year experience in process development and documentation
Job Type: Full-time
Benefits: Health insurance
Schedule:
* 8 hour shift
