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Gmp Consultant Jobs

1 - 10 van 102 vacatures

QA Validation Consultant

Pauwels Consulting

The responsibilities of the QA Primary Validation Consultant are among others:. The QA Primary Validation Consultant is part of the QA Operations for one MPU....

Indeed.com - 4 dagen geleden - 

Pharmaceutical consultant

QBD in Kontich, VAN

P, and then in particular with GMP and GLP. As pharmaceutical consultant , you can turn your hand to different types of projects:....

Indeed.com - 4 dagen geleden - 

CONSULTANT(E) Validation Systèmes Informatisés H/F

CVO-Europe in Waterloo, WBR

BPL, GMP et. Efficacement en équipe avec l'ensemble de vos interlocuteurs (clients et consultants). CVO-EUROPE assure des prestations de conseil, assistance...

Indeed.com - 18 dagen geleden - 

Validation consultant

Aerotek in Brussel

My client is a leading pharmaceutical company, specialised in biomedical products.In the context of investments projects in production, ensure proper execution of the validation methodology and application of GMP (Validation Master Plan, Design Qualification, Installation & Operational Qualification, Performance Qualification and Validation Reports) and specific regulations applicable to the “computer” domain (such as FDA’s 21 CFR Part 11 or Eudralex Annex 11)

stepstone.be - geleden 11 dagen - vacature opslaan - 

Validation consultant

Aerotek in Brussel

My client is a leading pharmaceutical company, specialised in biomedical products.In the context of investments projects in production, ensure proper execution of the validation methodology and application of GMP (Validation Master Plan, Design Qualification, Installation & Operational Qualification, Performance Qualification and Validation Reports) and specific regulations applicable to the “computer” domain (such as FDA’s 21 CFR Part 11 or Eudralex Annex 11)

stepstone.be - geleden 11 dagen - vacature opslaan - 

IT Consultant (H/F)

CVO-Europe in Waterloo

Degree in IT.- Experience in a pharmaceutical environment- Knowledge in GMP.- Knowledge in the SQLServer, SQL, XML/XSL, Windows 2000, XP, Vista and Macintosh, Window 7- Being familiar with the following concepts : OS, server platforms, storage, network, security, application delivery management systems, virtualization- Expert

stepstone.be - geleden 9 dagen - vacature opslaan - 

IT Consultant (H/F)

CVO-Europe in Waterloo

Your profile is :- Degree in IT.- Experience in a pharmaceutical environment- Knowledge in GMP.- Knowledge in the SQLServer, SQL, XML/XSL, Windows 2000, XP, Vista and Macintosh, Window 7- Being familiar with the following concepts : OS, server platforms, storage, network, security, application delivery management systems, virtualization- Expert

stepstone.be - geleden 8 dagen - vacature opslaan - 

Consultant en validation / qualification - nieuw

CVO-Europe in Waterloo

Avec plus de 250 collaborateurs, CVO-EUROPE est un groupe international implanté en France, Belgique, Suisse et aux États-Unis.Pour compléter l’équipe de notre Business Qualité / Validation, nous recherchons un(e) consultant en validation / qualification (H/F). Vous êtes en charge des différentes phases de validation :- définition et mise en oeuvre des opérations de validation (VMP, plan de validation, analyse de risques)- coordination et planification des activités

stepstone.be - geleden 1 dag - vacature opslaan - 

QA GMP Consultant

Harvey Nash IT Recruitment Belgium

Located in Walloon Brabant, Harvey Nash is currently looking for a QA GMP Consultant Location: Walloon Brabant Duration: 2 months (possibility of renewal) Scope of work: The QA GMP Consultant is responsible for all activities involving quality assurance and compliance with applicable regulatory requirements conducts audits and reviews/analyses data and documentation has knowledge of commonly-used regulations & guidelines (GMP) relies on instructions and pre-established guidelines reports to a supervisor

jobg8.com - geleden 30+ dagen - vacature opslaan - 

QA/GMP Consultant

Harvey Nash IT Recruitment Belgium in Brussel

Administrative support to management of GMP documents will be part of this role.Job responsibilities: Provide advice and support for technical Operational QA with a specific focus on:- Reviewing investigations- Reviewing specific deviation reports, complaint reports, changes and other risks that could impact product performance- Perform reviews of GMP documents- Administrative management of archiving of GMP documents Quality Agreements: support the drafting and signature

jobg8.com - geleden 30+ dagen - vacature opslaan - 

QA Consultant (GMP) - 12 months - Brussels Area

Brussel

Our client, one of the most prestigious multinational pharmaceutical corporation, is currently looking for a QA Consultant (GMP) 12 months Brussels Area Mission Description: You will work with the QA S Systems Continuous Improvement department in order to: Assure that all technical operations related to the analysis of pharmaceutical products comply with applicable regulations and guidelines (EMEA, FDA, PIC/S, ICH) Co implement technically robust and compliant systems allowing to exploit, maintain

xpatjobs.com - geleden 30+ dagen - vacature opslaan - 

QA Consultant (GMP) - 12 months - Brussels Area

belgium.expatjobs.eu in Brussel

Our client, one of the most prestigious multinational pharmaceutical corporation, is currently looking for a QA Consultant (GMP) 12 months Brussels Area Mission Description: You will work with the QA S Systems Continuous Improvement department in order to: Assure that all technical operations related to the analysis of pharmaceutical products comply with applicable regulations and guidelines (EMEA, FDA, PIC/S, ICH) Co implement technically robust and compliant systems allowing to exploit, maintain

xpatjobs.com - geleden 30+ dagen - vacature opslaan - 

Senior QA GMP Specialist

Harvey Nash IT Recruitment Belgium in Brussel

In the frame of a 6 months CMC project (possible extension), we are looking for a seasoned Consultant specialized in QA GMP to join a leading pharmaceutical company based in Brussels. Location: Walloon Brabant Duration: 6 months (possible extension) Scope of work: Operational Ensure the CMC project related QA activities are consistent across the range of different environments and teams supported (Vendors/Suppliers/in house) Ensure adequate documentation processes and systems are available and followed

xpatjobs.com - geleden 30+ dagen - vacature opslaan -