Product Quality Executive

PRESTIGE BIOPHARMA LIMITEDSingaporemycareersfuturefoilsithe 11/09/2026
Riachtanach:QA/TestLeadPrincipalJunior

Job Responsibilities

  • Lead in the implementation of Quality Management System in accordance with internal company policies and procedures, cGMP and other international regulations.
  • Update complaints retrieved from various sources to complaint log in a timely manner and escalate complaints into the CAPA system following review.
  • Participate in Product Quality activities by reviewing test protocols, reports, batch records and analytical data to ensure product quality meet the specified requirements.
  • Review OOS investigation, deviation, CAPA and risk management for products as required.
  • Review product quality documents and provide documents related to product quality upon request.
  • Draft and review Quality Technical Agreements
  • Provide management with quality data and trends as required.
  • Lead internal audits to ensure the effective implementation of Quality Management System as required.
  • Lead audits in DS and DP CMOs to ensure compliance to all relevant guidelines, regulations and agreements.
  • Provide training and guidance to personnel on quality assurance procedures, regulations, and best practices.
  • Mentor junior QA staff and contribute to their professional development.
  • Any other duties as assigned by supervisor.

Education/Qualification

  • Degree in Engineering (Biomedical) or Degree in Science (Biology, Chemistry,

Bio-engineering)

  • Experience in quality function dealing with Biopharmaceuticals with 3 to 5 years experience.
  • Experience in Bioprocessing Technology (Upstream and Downstream operations).
  • Minimum of 3-5 years of experience in pharmaceutical quality assurance, with a focus on product quality management and compliance.

Skills preferred

  • Strong analytical and problem-solving skill
  • Good computer skills, inclined to adapt to technology efficiently.
  • Results-oriented, multi-tasking, quick learner
  • Works independently and well under tight deadlines
  • Good knowledge and thorough understanding of cGMP, FDA regulations, ICH guidelines, and other relevant regulatory guidelines and quality standards.
  • Strong analytical skills and attention to detail, with the ability to critically evaluate data and identify trends.
  • Excellent oral and written communication skills, with the ability to effectively collaborate with cross-functional teams and communicate complex issues to diverse audiences.
  • Proven track record of conducting audits, investigations, and implementing corrective actions.
  • Team-player