QA Officer

The purpose of the position is to bring and maintain the validation of systems, processes, facilities and equipment within the organisation to the desired level. In doing so, the legal frameworks and in particular the pharmaceutical guidelines and regulations must be observed

and a strategy must be determined partly in consultation with the customers' quality managers.

• Performing internal audits and supervising external audits (internal, customers, notified bodies) in the context of validation.
• Setting up, implementing and securing validation studies (or having them set up), in consultation with staff from Operations, Supply Chain, Technical Services and QA .
• Documenting (or having documented) all validation activities and validation results.
• Contributing to the improvement and optimisation of staff, processes and systems and implemented procedures.
• Establishing procedures for the validation activities.
• Assessing the necessary validation in response to (proposed) changes in systems, processes, facilities or equipment.
• The validation of systems, processes, installations and equipment is initiated and implemented in a timely manner.
• The validation activities performed are of a good standard and comply with current international laws and regulations on validation and GMP.
• Changes made do not affect the validation status of systems, processes, installations and equipment.

• Bachelor or Master Industrial Sciences
• A few years of experience within a pharmaceutical production environment is a plus
• Known and familiar with GMP guidelines, pharmaceutical guidelines, knowledge of microbiology, hygiene, etc.
• Experience with quality systems, procedures, training, etc.
• Can work with MS-office
• Good knowledge of English (written and spoken)
• Experience in report writing
• Driven personality
• Leadership
• Ownership (sense of responsibility)
• Can organise work independently and set the right priorities, as well as work in a team.
• Purposeful
• Analytical and open-minded thinking skills

The company is part of a group and is responsible for the packaging and labelling of medicines. 

Permanent contract of unlimited duration.

Working within a strongly growing company. 
Attractive salary package with extra-legal benefits.

Questions or interest?

>> lommel@ctrl-f.be

>> 014 33 75 67 

>> WhatsApp: 0477 71 16 88