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Job Responsibilities
. 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.
. Perform internal audits to ensure the effective implementation of Quality Management System as required.
. Perform 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.
. Any other duties as assigned by supervisor.
Education/Qualification
. Degree in Engineering (Biomedical) or Degree in Science (Biology, Chemistry, Bio-engineering)
. Minimum of 2-3 years of experience in pharmaceutical quality assurance, with a focus on product quality management and compliance.
. Experience in Bioprocessing Technology (Upstream and Downstream operations).
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.
. Good 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
Date Posted: 20/11/2024
Job ID: 100972927