Job Description/Requirements
Responsibilities:
- Ensure implementation of Good Clinical Microbiology Practices.
- Manage essential laboratory equipment such as automated ID/AST analyzers, centrifuges, Class II biological safety cabinets, Vitek 2 compact system, and genomic including Polymerase Chain Reaction (PCR) technology.
- Design and implement relevant quality assurance and quality control standards, biosafety, hygiene, and infection prevention and control policies.
- Process data collection and reporting of AMR activities and monitor performance.
- Record and manage relevant program databases.
- Prepare monthly/quarterly program reports for stakeholders and present them to the Principal Investigator (PI).
- Engage with collaborators to review, analyze, and disseminate genomic and molecular data.
- Participate in research proposals, grant writing, abstracts, and manuscript development for international conferences and peer-reviewed journals.
Requirements:
- Minimum of MSc in Microbiology, Biomedical Science, or related field. An MBA or management qualification is a plus.
- 8 years of experience at a senior level in clinical microbiology or molecular biology laboratories.
- Proven expertise in managing laboratories, especially in Antimicrobial Resistance (AMR) testing and analysis.
- Proficiency in handling automated laboratory equipment such as ID/AST analyzers, Vitek 2 compact systems, PCR technology, and biosafety cabinets.
- Strong knowledge of Good Clinical Microbiology Practices, quality control, and biosafety protocols.
- Experience in data collection, analysis, and reporting related to AMR activities.
- Ability to maintain and manage laboratory databases and prepare reports for stakeholders.
- Involvement in research proposals, grant writing, and manuscript development for conferences and publications.
- Strong communication and collaboration skills for engaging with partners and disseminating genomic data.
- Strong leadership and organizational skills to supervise laboratory staff and ensure compliance with regulatory standards.
- Experience in developing and implementing quality assurance, infection control, and biosafety measures.
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