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GMP Validation Consultant

Trevalco
Aartselaar

Soumettre votre candidature

Détails de l'emploi

Temps plein

Avantages

Voiture de société
Chèques repas

Qualifications

Français
Anglais
Master
Expérience administrative
Esprit d'analyse
Compétences en communication
Néerlandais

Description complète du poste

Aartselaar, Belgium

A job as validation consultant in the pharmaceutical industry has a lot of variation. It includes technical analysis, document writing, execution of tests in production or laboratory environments, as well as a lot of interaction with different departments in the company where you work.

As validation consultant you execute validation projects on location at clients in the pharmaceutical industry.

This can be production equipment validation, lab equipment validation but it can also concern the validation of facilities and utilities, processes and computer systems. Depending on your background and interests you will be active in one or more of these areas.

For this position we are looking at all levels of experience, from starter to senior level.

Your responsibilities as validation consultant include:

develop a validation strategy which is realistic and meets current regulatory and client expectations, write validation plan and report
write URS
write IQ, OQ and PQ protocol
plan and execute or oversee execution of qualification tests
manage quality records such as deviations, CAPA's and change controls
participate to risk assessments and quality investigations
participate to internal and external audits
advise on pharmaceutical regulatory requirements such as GMP, GLP and GDP, taking into account current trends and future vision of the client
take decisions which properly balance out quality / budget / planning and help project stakeholders to reach a compromise on critical quality decisions

Customer relations

Personal development

Autonomy

Administrative work

Technical expertise

Must have

Fluent in English and Dutch.
Strong analytical skills, well organized, studious and precise.
You enjoy managing documentation: creating documents, reviewing and updating, getting approval on documents.
You can explain, you can convince, you can correct... you have perfect communication skills.
Master degree in science or engineering, or equivalent through experience.

Nice to have

Knowledge of French.
Knowledge of pharmaceutical regulations.

What is great about this job?

As a consultant, you will find yourself working with exciting companies in the Life Sciences sector.
You will use your knowledge and skills to tackle challenges faced by our clients.
A consultancy job can be a calling, or a springboard to the start of a career as a technical expert, people manager, or multipotential.
Trevalco is not a multinational with thousands of employees, but a Belgian SME, so you are not just a number with us.

What we offer

As an employer, we contribute to the success of your career. Proper guidance and training are very important to us. Naturally, we also ensure that you feel good in your job through a healthy work/life balance, a market-competitive salary, and tailored solutions for aspects such as mobility.

Salary

CAO90 bonus, hospitalisation and dental care insurance, meal vouchers and more

Mobility

you choose what works best: company car or mobility budget

Training

coaching, classroom or digital online training, what works for you

Work / life

because we have families, friends and hobbies

Soumettre votre candidature

Affinez votre recherche

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