Validation Engineer
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
We are currently looking for a Qualification & Validation Specialist to join a leading pharmaceutical manufacturing company based in the Walloon Region, Belgium. This is an exciting opportunity to contribute to critical qualification and validation activities within a dynamic team environment. The role offers the chance to support key projects related to production, assembly, and packaging activities, playing a crucial part in maintaining compliance and operational excellence.
The successful candidate will work remotely with some on-site presence, supporting both documentation and hands-on qualification activities for equipment and processes. This position is an initial temporary assignment with potential extension, ideal for professionals with proven experience in qualification and validation within the pharmaceutical or related industries.
This mission is for one year until end of 2027, and can offer between 600-675€ per day depending on experience.
Key Duties And Responsibilities
- Support the periodic review of qualification status and ensure compliance with quality standards.
- Execute qualification and validation activities for production, assembly, and packaging equipment.
- Work on qualification activities related to combination products and support packaging projects.
- Investigate deviations, technical issues, and propose appropriate solutions.
- As the Qualification & Validation Specialist, you will collaborate with stakeholders to ensure timely completion of activities and maintain accurate documentation.
Role Requirements
- A Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
- Proven experience of at least 3 years in Qualification & Validation within a regulated pharmaceutical environment, particularly with production and packaging equipment.
- Hands-on experience qualifying and validating equipment for manufacturing and packaging processes.
- Fluency in French, with the ability to read and write technical documentation in English.
- Availability and full commitment for the duration of the assignment.
Key Words:
Qualification / Validation / Pharmaceutical / Equipment Qualification / Packaging / Documentation / Compliance / French / Remote / Validation Activities
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements.
-
Validation Engineer
Il y a 16 heures
Brussel Hoofdstad, Brussel Hoofdstad, Belgique ELMEA Consulting Group Temps plein 55 000 € - 75 000 € ContratPlan, execute, and review qualification protocols (IQ, OQ, PQ) for equipment, utilities, and facilitiesPerform Computer System Validation (CSV) activities in line with GAMP 5 guidelinesAuthor and review validation documentation: VMP, URS, FS, DS, test protocols, and final reportsCollaborate with cross-functional teams including QA, IT, production, and...
-
Calibration & Validation Engineer, GMP Compliance
Il y a 3 jours
Brussel Hoofdstad, Brussel Hoofdstad, Belgique Prothya Biosolutions Temps plein 50 000 € - 75 000 € ContratProthya Biosolutions in Belgium is seeking a Calibration Maintenance Engineer to join our Maintenance team. You will serve as the technical expert for calibration and periodic validation activities across critical manufacturing and utility systems.The role requires a Master's in Industrial Engineering (Electromechanics) or equivalent, 1–3 years in a...
-
Validation Engineer: CSV
Il y a 16 heures
Brussel Hoofdstad, Brussel Hoofdstad, Belgique ELMEA Consulting Group Temps plein 55 000 € - 75 000 € ContratELMEA Consulting Group seeks a Validation Engineer to plan, execute, and review IQ/OQ/PQ protocols for equipment, utilities, and facilities. You will perform CSV tasks aligned with GAMP 5 and author comprehensive validation documents.In this role, you will collaborate with QA, IT, production and engineering, manage deviations and CAPAs, and support...
-
Life Sciences Computer system validation engineer
Il y a 5 jours
Brussel, Brussel Hoofdstad, Belgique Sopra Steria Temps plein 45 000 € - 65 000 € Contrat2 days ago Be among the first 25 applicantsDescription De L'entrepriseSopra Steria propose des solutions technologiques et logicielles sur mesure, de bout en bout, pour aider ses clients à faire des choix audacieux et à obtenir des résultats. Et ce, avec succès ! Avec plus de 51 000 collaborateurs dans 30 pays, nous sommes le leader européen des...
-
Railway Systems Engineer — Validation
Il y a 4 jours
Brussel, Brussel-Hoofdstad, Belgique Free-Work UK Temps plein 45 000 € - 65 000 € ContratViveris is seeking a Systems Engineer to join our client's project engineering team in the railway sector. You will define, verify, validate and integrate subsystems (doors, brakes, etc.) to ensure safety and reliability across the system.You will write system specifications, plan testing, analyse results, and coordinate between customers and internal teams...
-
Engineer Maintenance Calibration/Validation | Brussels
Il y a 3 jours
Brussel Hoofdstad, Brussel Hoofdstad, Belgique Prothya Biosolutions Temps plein 50 000 € - 75 000 € ContratAt Prothya, we are committed to delivering life-saving plasma-derived therapies that improve patients' lives worldwide. To support our growing operations, we are looking for a Calibration Maintenance Engineer to join our Maintenance team.As the technical expert for calibration and periodic validation activities, you will play a key role in ensuring the...
-
Senior Engineer QA Validation | Brussels
Il y a 4 jours
Brussel Hoofdstad, Brussel Hoofdstad, Belgique Prothya Biosolutions (operating under Accord Plasma B.V. / Intas Pharmaceuticals) Temps plein 90 000 € - 120 000 € ContratReports to the Supervisor QA (A.I.)ObjectivesAs a Senior Quality Engineer, you safeguard quality levels by monitoring and ensuring that all operations at all levels are carried out in accordance with the cGMP quality systems applied within Prothya Biosolutions. In this way, you contribute to Prothya Biosolutions’s pharmaceutical products meeting European...
-
Senior QA Validation Lead – cGMP
Il y a 4 jours
Brussel Hoofdstad, Brussel Hoofdstad, Belgique Prothya Biosolutions (operating under Accord Plasma B.V. / Intas Pharmaceuticals) Temps plein 90 000 € - 120 000 € ContratProthya Biosolutions, a Belgium-based biopharmaceutical company, seeks a Senior Quality Engineer to safeguard quality by overseeing qualification and validation protocols from a QA perspective. You will review validation protocols and reports and draft validation tests for equipment, utilities, IT, cleaning, and process validation.You will lead...
-
Senior IT Specialist – Computer System Validation
Il y a 3 jours
Brussel Hoofdstad, Brussel Hoofdstad, Belgique Agidens Temps plein 70 000 € - 110 000 € ContratBen jij een ervaren IT-professional met een sterke technische achtergrond en ervaring binnen een GMP-omgeving? Begrijp je hoe moderne software, IT-infrastructuur en dataomgevingen zijn opgebouwd en wil je jouw expertise inzetten binnen de farmaceutische industrie? Dan zoeken wij jou! Wij zijn op zoek naar een Senior IT Specialist die complexe IT-systemen kan...
-
Qualification & Validation Coordinator – Life Sciences
Il y a 4 jours
Brussel, Brussel-Hoofdstad, Belgique SmartRecruiters, Inc. Temps plein 60 000 € - 90 000 € ContratFull-timeContract Type: PermanentCompany DescriptionALTEN is a world leader in Engineering and Technology Consulting with almost 60 000 employees, 88% of whom are engineers.Operating in more than 30 countries, the Group supports its customers' development strategy in the areas of engineering, innovation, R&D and technological information systems.Why choose...