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Gmp Consultant Jobs

1 - 10 van 101 vacatures

QA CSV

belgium.expatjobs.eu in Antwerpen

For a leading pharmaceutical company we are searching for a consultant/candidate available for a new assignment in computer system validation. Please ... find bellow the Job description : General Mission: To assure that all CSV related regulatory requirements are fulfilled during the complete life cycle (concept, project, operational and retirement phase) for the client's computerised systems. Specific Missions: Maintain the Validation Master Plans up to date and ensure timely execution. Review and approve

xpatjobs.com - geleden 11 dagen - Meer details - 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 - Meer details - 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 - Meer details - 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 - Meer details - 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 - Meer details - 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 - Meer details - 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

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

Validation Consultant with experience in GMP and SAP

Harvey Nash IT Recruitment Belgium in Brussel

One of our clients, a multinational company in the pharmaceutical industry currently requires a Validation Consultant with experience in GMP and ... SAPStart: 15/8/13Length: min. 2 monthsLocation: South of BrusselsFUNCTION DESCRIPTION:Responsability for validation of a new SAP module in replacing an old computer system obsoleteKEY RESPONSIBILITIES. Participate in the revision of new SAP module's URS. Writing of the project charter. development of validation test: Writing and realization according to

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

QA Consultant

belgium.expatjobs.eu in Brussel

Our client is an engineering company and is looking for a QA Consultant to join a QA project at a pharmaceutical company. The QA Consultant will work at ... our client in Belgium for at least 1 year. Scope of work: join a team working on a QA project linked to filling activities be in charge of GMP deviations: investigation, analysis, writing, review, execution/implementation/coordination Requirements: mandatory: knowledge and experience ( 4 years, max. 15 years) in filling (liquid lyo), in sterile/aseptic

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

QA Consultant

Harvey Nash IT Recruitment Belgium in Brussel

Our client is an engineering company and is looking for a QA Consultant to join a QA project at a pharmaceutical company. The QA Consultant will work at ... our client in Belgium for at least 1 year. Scope of work: join a team working on a QA project linked to filling activities be in charge of GMP deviations: investigation, analysis, writing, review, execution/implementation/coordination Requirements: mandatory: - knowledge and experience (> 4 years, max. 15 years) in filling (liquid & lyo), in sterile/aseptic

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