Position Overview
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We are seeking an experienced QA/QC Manager to lead and strengthen AcroCyte’s quality management function. This role will be responsible for the development, maintenance, and continuous improvement of the company’s Quality Management System (QMS), while providing leadership and oversight across quality assurance and quality control activities.
The QA/QC Manager will work closely with manufacturing, laboratory, research, and cross-functional teams to ensure that operations are performed in accordance with established quality standards, internal procedures, and applicable regulatory requirements. This position will also lead internal and external audits, oversee supplier quality activities, and manage the QA/QC team to drive consistent execution and continuous improvement.
This is a key leadership role for an experienced quality professional who combines strong technical knowledge with practical problem-solving, team leadership, and the ability to build an effective quality culture in a growing biotechnology organization. -
This is a full-time position at AcroCyte Therapeutics in New Taipei City, Taiwan.
About AcroCyte
AcroCyte Therapeutics is a pioneer in advanced translational medicine, leading the development of next-generation scaffold-free 3D organoid cultures derived from human patient samples. By bridging the gap between complex in vitro models and clinical reality, we are driving the future of next-generation liquid biopsy platforms and precision oncology to accelerate therapeutic discovery and patient care.Key Responsibilities
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Lead the development, implementation, maintenance, and continuous improvement of the company’s Quality Management System (QMS).
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Ensure quality systems and operational activities remain aligned with applicable regulatory requirements, industry standards, and internal procedures.
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Provide oversight of QA/QC activities supporting manufacturing, laboratory, and related operational functions.
- Monitor quality-related processes to ensure activities are performed consistently and in accordance with established procedures and quality standards.
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Plan, coordinate, and lead internal and external quality audits.
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Manage supplier qualification, evaluation, monitoring, and periodic review activities.
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Work with suppliers and internal stakeholders to address supplier-related quality issues and maintain appropriate quality documentation.
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Lead, coach, and develop the QA/QC team to strengthen technical capability, accountability, and execution.
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Collaborate closely with manufacturing, laboratory, R&D, operations, and other functions to resolve quality-related issues.
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Facilitate clear and constructive communication across departments while maintaining appropriate quality standards.
Minimum Qualifications
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Bachelor’s degree or higher in Biotechnology, Biomedical Sciences, Biology, Chemistry, Pharmacy, Biomedical Engineering, or a related life-science field.
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10+ years of professional experience in the biotechnology, pharmaceutical, medical device, or related life-science industry.
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At least 5 years of hands-on QA/QC experience.
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At least 2 years of experience managing or leading a team.
- Strong knowledge and practical experience with ISO 13485 Quality Management Systems.
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Full professional proficiency in English and Mandarin, with strong written and verbal communication skills.
Preferred Qualifications
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Experience in cell therapy, regenerative medicine, or other advanced biotechnology applications.
- Hands-on experience working in GMP- or GTP-regulated facilities or environments.
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A strong commitment to quality and a willingness to take ownership of quality-related decisions and outcomes.
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Effective leadership skills with the ability to coach, develop, and motivate a QA/QC team.
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Clear, logical thinking and a structured approach to investigating and resolving quality issues.
How to Apply
Send your resume to buddy@acrocyte.com. Please include the position title in the subject line.
You may also choose to submit your resume through 104 Job Bank.