QC Microbiology Analyst
On-siteVictoria, Central and Western, Hong Kong
Job Summary
Conduct internal audits of R&D and Quality laboratories to ensure readiness for regulatory agencies' audits. Ensure compliance with regulatory policies, procedures, and practices by identifying discrepancies in product safety and recommending corrective actions. Maintain laboratory areas, equipment, and facilities in a clean, orderly, and operational state while performing verification or calibration of instruments for annual product review. Develop good working practices and guidelines for staff to use quality system Standard Operating Procedures, managing review and approval of Building Management System Alarms. Lead the Continuous Improvement (CI) process for Integrated Manufacturing Excellence (IMEx) within the Drug Product unit, identifying and conducting continual improvement projects.
Required Qualifications
- BA/BS degree
- Associate's degree with 4+ years of experience
- high school diploma (or equivalent) with 6+ years of relevant experience
- Solid understanding of common laboratory databases
- Familiarity with regulatory compliance requirements for pharmaceutical manufacturing
- Ability to work effectively both independently and as part of a team
- Proficiency in using quality system Standard Operating Procedures
Desired Qualifications
- Experience in a pharmaceutical microbiology laboratory
- Strong problem-solving skills
- Ability to manage multiple tasks and projects simultaneously
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity
- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
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