I’m working exclusively with my Biotechnology Client in Belgium, which is in urgent need for an interim QA Sterility Assurance Manager to ensure the quality monitoring of projects, participate in the management and improvement of the quality of pharmaceutical production meeting GMP standards.
Reason for the role being open is due to the fast growing projects of the organisation; so an initial 6 month interim contract is offered to a suitable consultant. If interested, send your CV to firstname.lastname@example.org ASAP, since interview + offer will take place this week.
Start Date: ASAP / Duration: 6 Months / Hours: 40 per week (1 or 2 days working from home is possible)
Implement standards in terms of sterility assurance within a GMP environment
Ensure the role of Expert for the implementation and development of a CCS (Contamination Control Strategy)
Follow the mitigation plan for the implementation of the CCS (Contamination Control Strategy)
Support Production / Quality Control / Quality Assurance / Technical Services & Validation teams
Minimum 5 years of experience in the pharmaceutical industry in quality assurance
Very good knowledge of the quality system (Deviation, CAPA, change control, risk management, ...)
Knowledge and/or experience/expertise on topics/areas related to sterility assurance (Contamination Control Strategy, aseptic practices, environmental & clean fluid monitoring, cleaning/disinfection, sterilization, aseptic simulation, ...)
Interview process: 1 stage interview process via Teams