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VALIDATION ENGINEER
Poulpharm —Izegem
- Master
- Bachelier
- IT
- Travail à domicile
il y a 12 jours
senior software developer
Poulpharm —Izegem
- Azure
- Systèmes PGI
- Développement logiciel
- Remboursement des frais de téléphone
- Travail à domicile
il y a 4 jours
Quality Officer
Poulpharm —Izegem
- Formation continue

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VALIDATION ENGINEER

Poulpharm
Izegem

Soumettre votre candidature

Détails de l'emploi

Il y a 12 jours

Avantages

Voiture de société
Chèques repas
Travail à domicile

Qualifications

GxP
Master
Bachelier
IT
Néerlandais

Description complète du poste

At Poulpharm, we believe in the potential of every individual to make a positive impact on veterinary healthcare.

Our dedicated team of professionals – ranging from laboratory technicians, animal carers, researchers and species experts to marketers and quality coordinators – works tirelessly together, both at the diagnostic level and when conducting (pre-)clinical trials in our own state-of-the-art testing facilities.

Acting as a bridge between our IT and QESH teams in Belgium, Poulpharm is looking for a Validation Engineer.

Are you fascinated by quality, IT and validation? Do you enjoy working in a structured manner and do you thrive on ensuring GxP compliance within an international environment?
If so, you might be the validation engineer we are looking for.

Job description

As a Validation Engineer, you will ensure that our computerised systems comply with the applicable quality and regulatory requirements.

Your responsibilities will include, amongst other things:

Overseeing the entire validation lifecycle of computerised systems, from implementation to decommissioning.
Drawing up, implementing and maintaining validation documentation, such as validation plans, user requirements, risk analyses and test protocols.
Monitoring the validated status of systems by correctly tracking changes, periodic reviews and corrective actions within MasterControl.
Ensuring compliance with applicable quality guidelines, regulations and data integrity principles.
Collaborating with IT, QESH, the various laboratories and external suppliers on the implementation, modification and validation of systems.
Supporting internal and external audits and assisting with the follow up of audit findings.
Drawing up user procedures and providing training to ensure systems are used correctly and in accordance with requirements.

To this end, you will work closely with colleagues from the QESH-team, IT, the various laboratories and external partners.

profile

A master’s or bachelor’s degree in a scientific, (bio)technical or IT discipline, or equivalent experience.
You have 3 to 5 years’ relevant experience in computer system validation within a GxP environment.
You are familiar with relevant quality guidelines and regulations, such as GAMP 5, ISO
standards, data integrity and the applicable regulations for validated systems.
You work accurately and in a structured manner.
You are able to work independently and take responsibility for your projects.
You enjoy collaborating with different teams.
You communicate fluently in Dutch and English.
Experience with MasterControl and/or Testo is an advantage.

what do we offer you?

A varied role in which you help to ensure and build a smooth compliance process
Opportunities for personal growth and further development
An attractive salary package, tailored to your experience and expertise, supplemented by meal vouchers, hospitalisation and health insurance, a mobile phone allowance and a company car with a fuel/charging card
The option to work from home
A 40-hour working week with 12 days of compensatory time off
Flexible leave to ensure an optimal work-life balance
A corporate culture centred on collaboration, team spirit and fun, with after-work drinks and regular team events

If you are interested in joining our team, please send your CV and motivation letter to
[email protected].

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facility coordinator emplois - west vlaanderen

VALIDATION ENGINEER

senior software developer

Quality Officer

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