Quality Assurance Manager (Pharmaceutical)

Getz Pharma Philippines

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Di tempat - Pasig3-5 Tahun KedaluwarsaS1Penuh waktu
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Deskripsi Pekerjaan

Keterangan

The purpose of this role is to ensure the safety and quality of Getz Pharma Phils., products by overseeing the collection, assessment, and compliance with local and international regulatory requirements.


Responsibilities


  • Works with the Quality Assurance Supervisor and the Quality Director, also the Deputy Management Representative (MR) in the design, development, implementation and continual improvement of the company’s management system.
  • Handless the over-all Validation & Qualification Program of Getz Healthcare.
  • Manage & analysis of Quality data for the organization.
  • Supervise and direct quality assurance associates who are responsible for ensuring the effective implementation of Quality Management System on their respective sites and other quality-related policies in order to meet product quality standard.
  • Conducts mentoring, training and performance evaluation to Quality Associates to ensure good performance.
  • Ensures that all issues and concerns regarding Quality are immediately acted upon and/or reported to the Quality Assurance Director or to the concerned departments.
  • Assists in investigating and correcting quality-related issues (including customer complaints) through collaboration with other departments.
  • Ensure compliance to Deviation Management and Change Management Procedures.
  • Conducts training on quality-related procedures and standards such as GMP, GDPMDD, ISO 9001 and RQA Guidelines.
  • Act as a Lead in EMS Programs.
  • Works with the Systems and Compliance Officer and Internal Quality Audit Team in conducting routing operational audit to ISO 9001:2015, good distribution and storage practices, and good manufacturing practices compliance.
  • Attends the internal, client or external audits, regulatory visits/inspections/audits, and audits of the third party service providers. Raise Corrective and Preventive Action (CAPA) Report on the identified nonconformities.
  • In coordination with the various site Managers, may lead the Client audits and other external audits in the sites as the need arises.
  • Coordinate and follow through with the Process Owners for the submission of corrective actions on non-conformity reports or deviations. Report to Management on the performance of the Quality Management System as well as the non-conformities observed.
  • Assists in complying with audits/routine inspection from Regulatory Bodies (FDA/PDEA) and other government agencies.
  • Act as internal auditor in the conduct of the Internal Quality Audit.
  • Assist in preparing audit program, plan and conduct internal audits / inspections in the specified branches to check on operational departments’ compliance to established procedures, ISO 9001, GSDP, GDPMDD, cGMP, regulatory and other international standards requirements as well preparation for Clients, Regulatory or other external audits.
  • Ensures compliance to client, regulatory requirements, international standards and procedures applicable to the Distribution Center.
  • Spearheads quality programs and initiatives for continual improvements by driving improvements activities or changes in processes or systems through coordination with cross functional project teams.
  • Make proactive recommendations to the Quality Assurance Director to improve quality and work efficiency.
  • Ensures recording and timely reporting of periodic Management Reports such as Quality KPIs.
  • Collates data and does comparative analysis of performance to serve as point of reference for process improvements.
  • Signs and approves documents within level of authority.
  • Prepares and provides the reportorial requirements of the company and principals as requested.
  • Recommends managing the necessary interventions, policies, and procedures that will make the delivery of the function’s objectives effective and efficient.
  • Perform other job functions as directed by the Quality Director from time to time or as may be necessary in support of company objectives.


Qualifications

  • A minimum of a bachelor’s degree in Pharmacy, Medicine Life Sciences or related field.
  • A minimum of 3-5 years of experience in Quality Assurance and Management System with demonstrated experience in Regulatory Compliance, Safety Reporting and Risk Management.

Persyaratan

Please refer to job description.

Manajemen mutuTest PlanningTugas beresikoPeningkatan ProsesTeam LeadershipPenyelesaian masalahCompliance StandardsAutomation TestingPengujian Kinerja
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Boss

HR ManagerGetz Pharma Philippines

Lokasi Kerja

10/F One Filinvest Ortigas Center, Pasig City, Metro Manila, PH

Diposting di 28 May 2025

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