Science & Innovation Scientist Ftc

4 weeks ago


Cape Town, South Africa SciStaff Full time

Bachelor’s degree or diploma in Microbiology/Biochemistry/Chemistry/Process Engineering or equivalent and relevant hands-on experience or at least 2-3 years’ practical experience in a similar position. Ability to work under biosafety level 3 containment._
- Location:

- Cape Town
- Description:

- A leading vaccine manufacturer is seeking a Scientist to join their Science and Innovation team. This is a 6-month fixed-term contract position and the duties and responsibilities of the role include, but are not limited to, Laboratory Administration, including Budgeting and Cost Control; Ensure services are delivered to all internal and/or external stakeholders as defined and as per agreed timelines; Risk and Anticipation Mitigation to ensure that all work done is in accordance with current standards/processes and assist Senior Scientist/Group Leader to identify anticipated risks impacting the group/unit/team; Follow cGMP guidelines and ensure all Change Controls/NCR’s etc. are effectively managed to support QA’s processes; Mitigate obvious risks on site and submit job cards to address facility issues/risks as per the process set by Engineering; Close all actions assigned to self/staff member as per EHS committee agreed deadlines; Responsible for providing assistance, guidance, problem solving or input to the operational departments as required and agreed; Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines; Responsible for biological product and process development, which could include upstream (microbial cultivation) and down-stream processes (purification) and analytical method development (microbial, immunological, chemical); Responsible for experimental design, planning, execution, problem solving and recording; Assist with technology transfers from development to manufacturing (including manufacture of material to be used in clinical trials); Responsible and accountable for the generation of applicable documentation in accordance with current scientific, GMP and GDP guidelines; Driving Innovation and Continuous Improvement; and Compilation of Deviations, Change Controls, and CAPAs.
- Key Requirements:

- A Bachelor’s degree or diploma in Microbiology/Biochemistry/Chemistry/Process Engineering or equivalent with relevant hand-on experience or at least 2-3 years practical experience in a similar position. Sound knowledge and experience in Product development of vaccines and/or biologicals and associated equipment. Exposure and understanding of scientific principles that governs the production of vaccines and/or biologicals. Knowledge of cGMP (SA, PIC, WHO) and GLP guidelines. Knowledge of bio-safety principles and the ability to work under biosafety level 3 containment. Experience in having successfully faced local quality audits would be advantageous.
- Additional Requirements:



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