A biotechnology company is seeking an experienced QA Referent
Writing and implementation of SOPs and relevant QA documents.
Document control and management.
Close interface with the Company’s personnel from all departments.
Perform investigations of deviations and OOS.
Lead CAPAs and change controls processes.
Execute QA internal and external audits.
Work under GMP guidelines.
Report to the QA Manager
Requirements:
Education: BSc /MSc or equivalent in Biology, Biotechnology, Biological Sciences, Bio-Medical Engineering.
2 – 3 years’ experience in the field.
Experience in cell therapy – a major advantage.
Experience with QA-QC interface – an advantage.
Previous work experience in a GMP environment.
Team player with very good interpersonal skills.
Excellent oral and technical writing skills in English.
Assertive, accountable and responsible.
Ability to multitask and work independently under stressful conditions.
Organized with great ability to work with high level of detail.
The position applies to men and women alike.
