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QA Officer

Hamont Achel
Fixed
39 hours per week
Chemistry
46526
Reference: 46526
Date: 2024-02-15
Sharon Sannen
Recruitment Partner
014/337 567
014/337 567
sharon.sannen@ctrl-f.be
Technical Engineering Lommel
lommel@ctrl-f.be
Vreyshorring 49, 3920 Lommel
69103
18152
https://wa.me/32477711688

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

Function

The purpose of the position is to bring and keep the validation of systems, processes, installations and equipment within the organisation to the desired level. 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, 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 required validation in response to (proposed) changes in systems, processes, installations or equipment.
  • The validation of systems, processes, installations and equipment is initiated and implemented in a timely manner.
  • The validation activities carried out are of a good standard and comply with the current international legislation and regulations in the field of validation and GMP.
  • Changes made do not affect the validation status of systems, processes, installations and equipment.

Organisation

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

Profile

  • 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

Apply for this vacancy.

We will get back to you as soon as possible.

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