This role requires working on-site exclusively, with no other working option available.
To confirm with all site quality management systems and health & safety procedures (ISO17025:2017, ISO15189:2012, GCLP, Human Tissue Act (2004))
Monitor project progress and quality, effectively communicate with relevant teams/departments; ensure projects are delivered within the turnaround time (TAT) and meet the quality requirement
Formulate and update the production plans according to projection, arrange pipeline to ensure smooth operation, optimize NGS protocols and automation of laboratory procedures.
Instruct team leaders to carry out production data summary and statistical analysis. Ensure all relevant information are documented and archived. Be responsible for conducting department's reports.
Establish responsibilities for members by roles and technical levels, supervise them to perform their duties
Other tasks assigned by the line manager.
*Requirements:**
A Master's or advanced degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of three-year laboratory experience.
Experiences in leading a team of 5-10 members (minimum). Strong teamwork ethic and the commitment to successfully deliver to tight deadlines are essential.
High accuracy and attention to detail are a must for both laboratory and office-based work.
A strong and open communication skills is essential.
Fluent operating Microsoft Office software including Word, Excel and PowerPoints is essential.
Experience of using Laboratory information management systems (LIMS) is advantageous.
Experience in PCR, qPCR and Next-Generation Sequencing (NGS)-based analysis is advantageous.
Very good knowledge of German and English language, both written and spoken. Knowledge of Chinese will be an added advantage.
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