Quality Assurance StaffArkray Industry, Inc.
Workplace: Batangas
Salary: Agreement
Work form: Full time
Posting Date: 19/04/2024
Deadline: 07/03/2024
Duties and Responsibilities:
Monitor and checking processes according to company's policies, procedures and standards.
Participate in Corrective and Preventive Action (CAPA) Root Cause Analysis and Continuous Improvement (Kaizen) Activities.
Ensure that product meets specification requirements by analyzing test results for applicability, accuracy documenting required data/information.
Ensure CAPA / audit observations response are appropriately implemented and closed in a timely manner.
Provides general support to quality team during audit and other related inspection activity.
Assists in the creation, review and improvement of documentation.
Qualification:
Preferably with bachelor's degree in any engineering or business-related course
With at least three years of relevant experience in a manufacturing set-up, preferably from an ISO 13485 (Medical Devices) certified company
Qualified auditor or has experience with QMS Audits is an advantage.
Experience in US FDA audits handling is an advantage.
Can create QMS procedures and can judge suitability of work instructions and procedures.
Applicants may also send their comprehensive resume with colored recent picture at [Protected Info] / [Protected Info] and indicate position applied for as the "subject".
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Monitor and checking processes according to company's policies, procedures and standards.
Participate in Corrective and Preventive Action (CAPA) Root Cause Analysis and Continuous Improvement (Kaizen) Activities.
Ensure that product meets specification requirements by analyzing test results for applicability, accuracy documenting required data/information.
Ensure CAPA / audit observations response are appropriately implemented and closed in a timely manner.
Provides general support to quality team during audit and other related inspection activity.
Assists in the creation, review and improvement of documentation.
Qualification:
Preferably with bachelor's degree in any engineering or business-related course
With at least three years of relevant experience in a manufacturing set-up, preferably from an ISO 13485 (Medical Devices) certified company
Qualified auditor or has experience with QMS Audits is an advantage.
Experience in US FDA audits handling is an advantage.
Can create QMS procedures and can judge suitability of work instructions and procedures.
Applicants may also send their comprehensive resume with colored recent picture at [Protected Info] / [Protected Info] and indicate position applied for as the "subject".
Sharing is Caring
We know that resume is a must to apply for a job. If you don't have one or yours is already obsolete. HireMe.ph gives you free editable resume templates
Hireme.ph
Other Info
Santo Tomas, Batangas
Permanent
Full-time
Permanent
Full-time
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Arkray Industry, Inc.
About the company
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