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QA Manager (Pharmaceutical or Medical Devices Industry)

RM 8,000 - RM 10,000 / Per Mon

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Key Responsibilities:

To act as Quality Liaison personnel in ensuring the Quality Management System are being exercised and implemented as per regulatory requirements (ISO9001:2015, ISO13485:2016, GMP, GDP, GDPMD) and Principal Requirements.

Job Scope:

  • Develop and implement Quality Management System (QMS) as per requirements (ISO 9001:2015, ISO 13485:2016, GDP, GMP, GDP and GDPMD) and customer/principal requirements.
  • Coordinating company Annual Management Review Meeting (MRM) and follow – up identified action required after the meeting.
  • Develop, Review and Maintain the company adherence to SOPs, WIs and Forms as per Quality Management System (QMS) requirements.
  • Oversee and ensure the Non-Conformance is log timely, reviewed and close with effective action taken.
  • To oversee and ensure the customer complaint is log timely in the software, reported and close timely.
  • To oversee and ensure Corrective Action and Preventive Action (CAPA) are taken with effective measures.
  • Coordinate and maintain the Training Program sitewide as per internal SOP, regulatory requirements and principal requirements.
  • Monitor external Service/Product provider performance as supplier Management Program.
  • To oversee and ensure Supplier Corrective Action Report (SCAR) are taken with effective measures.
  • To lead and coordinate Internal Audit Program activities as per requirement (ISO 9001: 2015, ISO 13485:2016, GDMPD, GDP/GMP)
  • Lead and Coordinate External Audit from Authority, Principal and CAB as per requirement (ISO 9001, ISO 13485, GDMPD, GDP/GMP)
  • Lead and coordinate the Change Control Program as per internal SOPs and requirements (ISO9001:2015, ISO13485:2016, GMP, GDP, GDPMD Principal Requirements).
  • Lead and Coordinate Temperature Mapping Program as scheduled and according to requirements (GDP)
  • Lead and Coordinate Validation and Qualifications Program as scheduled and according to requirements (GDP)
  • Lead and Coordinate Redressing and / or Relabeling for Pharmaceutical and Medical Devices Product
  • Lead and coordinate new and/or potentially Customer and Principal Integration and Migration
  • To assist incoming product release (Pharmaceutical and Medical Devices) as per requirements.
  • To prepare and approved incoming product redressing / relabeling (Pharmaceutical and Medical Devices) as per requirements.
  • To review and approved monthly services report of Pest Control, Temperature Recording, Facility cleaning and Monitoring.
  • To review and verify 3PL redressing, product return and NFHU conversion as per principal requirement.
  • To review new and/or existing Quality Technical Agreement with Principal as per principal requirement
  • To be contact personnel for liaise with Principal regarding any changes, audit, meeting, documentation and request according to principal requirement
  • To attend the monthly Country Business Review reporting departmental KPI, risk and compliance as per requirement ISO9001:2015, ISO13485:2016, GMP, GDP, GDPMD Principal Requirements).
  • Develop and foster strong professional relationships with regulatory authorities and professional bodies.
  • Provide insight and advice on all activities or matter associated with Quality Assurance System, Medical Affairs and Pharmaceutical compliance of the company.
  • Supervising and providing technical support and guidance to Operation Department for Quality Assurance matter related.
  • To participate and assist during annual Regulatory Affairs department Precursor Audit by Authority (NPRA)
  • To plan and conduct the Pharmacovigilance Audit to Regulatory Affairs department annually according to requirement (QMS and GVP)

Key Requirements:

  • Work experience in the Pharmaceutical and/or Medical Devices industry for a minimum of 10 years.
  • Managing role experience for a minimum of 2-3 years.
  • Knowledge on QMS (ISO 9001:2015, ISO 13485:2016, GDPMD, GDP/GMP)
  • Auditing experience in Pharma and MD
  • Lead Auditor certified (IS0 9001: 2015) or GDP would be added advantage.

Job Types: Full-time, Permanent

Pay: RM8,000.00 - RM10,000.00 per month

Schedule:

  • Monday to Friday

Education:

  • Bachelor's (Preferred)
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