Senior Laboratory Technician - Study Delivery (MEA) · Cape Town at Synexa Life Sciences

Main areas of responsibility:

• Ensures that all samples are processed according to the sample analysis plan as well as timely delivery of study deliverables.
• Assists in the laboratory with tasks associated with Method Development and Validation, under the supervision of the APM/ Senior Scientists.
• Is able to work on multiple platforms with minimal supervision.
• Works as the main analyst on multiple studies at any given time.
• Is able to troubleshoot methods and instruments on a technical level
• Ensures that the Odoo planning app is accurately and efficiently updated
• Generates revenue by processing clinical samples and performing Method Development and Validation work as per Method Sheets
• Provides support to up to 10 team members and oversees their work and training
• Ensures study teams work with minimal errors (data and paperwork) and supports members in executing preventative actions
• Ensures the upkeep of Study Files and documentation
• Identifies and document deviations within the study
• Assumes a leadership role in training team members on specific aspects of multiple studies, methods and company procedures
• Oversees and drives the performance of team members while setting an example for others; is a strong driver of teamwork
• Manages equipment which includes being custodian of a range of equipment and identifies issues, including troubleshooting.
• Ensures reagent orders are within the budget of quote, is involved in reagent planning and management
• Supports the writing of reports and documents for projects (Lab Manuals, Validation Phase Plans, Method Development Plans, Sample Analysis Plans, Sample Analysis Reports etc.)

Ad-hoc

• Creates customer satisfaction by flawless study execution and oversight on selected studies and shows good verbal communication with key players.
• Strong adherence to regulatory compliance and safety requirements, involving good clinical laboratory practices (GCLP), SOPs, Health & Safety policies, and other related documents.
• Assesses systems being used, identifies gaps and identifies areas for improvement.
• Writes, maintains and reviews SOPs and forms.

Qualification/Experience:

• A minimum level of vocational training as a Medical/Biomedical laboratory technician (i.e., National Certificate in clinical pathology from recognized institution) with 4-5 years of experience in the equivalent work or in a relevant technical role.
• On-going general International Organization for Standardization - ISO, Good Clinical Practice - GCP and Good Laboratory Practice - GLP awareness training needs to be provided to all staff. The job holder needs to ensure that he/she is up to date with the available training.
• Experience in pipette handling, following protocols, and using basic equipment (e.g., centrifuges, biosafety cabinets, incubators). Can independently troubleshoot equipment-related problems and perform multiple assays.
• Working within a good practice (GxP) and/or Good Clinical Laboratory Practice (GCLP) accredited environment.
• The ideal candidate should have prior experience working with analysers (MSD, Epoch), Flow cytometers, PCR.
• Someone who has a strong understanding of the day-to-day operations within a laboratory and who has a strong ability to lead, train others, and influence their productivity.