Gmp Audit/compliance

Location:Wavre Type:Contracting#20811GMP ComplianceBrabant Wallon - contractingOur partner is looking for a GMP Compliance to join its team. This international company is well-known for its pharmaceuticals products.What are your responsibilities?The purpose of the role is to support the operation QA team to assure and maintain the organization of the...

Location:Wavre#22053GMP Compliance:Wavre - contractingOur partner is looking for a QA Regulatory Compliance to join its team. This international company is well-known for its pharmaceuticals and vaccines.What are your responsibilities ?: Review and/or approval of variations/submissions/RTQ/Commitment + provide technical support to GRA You support...

**_Votre défi :_**- Conduire et suivre des audits internes dans les laboratoires (chimie et Projects & Stabilities):- Mener des audits auprès du personnel de laboratoires, relever les incohérences, les dysfonctionnements- Evaluer les systèmes et les techniques de travail utilisées en regard des procédures et législations applicables- Rédiger les...

Site Name: Italy - Siena, Belgium-WavrePosted Date: Aug Specialist R&D Third Party Quality GMP/GDP (maternity leave)Job Purpose:Ensure QA Oversight of third parties involved in the Clinical Manufacturing and Supplies environment (including batch review activities). Be the quality contact of the RDC for all GMP topics.Key Responsibilities: Be the quality...

**_Votre défi :_**- Rédiger et/ou assister au développement, à la révision, à l'implémentation de documents QA par rapport au GMP ;- Signer les protocoles et rapports (dans le respect des procédures) ;- Approuver tous les documents au niveau QA ;- Réaliser des audits internes et défend le système qualité lors des audits externes ;- Coordonner,...

Site Name: Belgium-WavrePosted Date: Feb This role will need you to provide Independent Quality Assurance to GSK R&D, by delivering the audit program including defining scope, conducting audit processes, reporting observations and ensuring delivery of audit report. You will identify compliance issues, monitor trends, be accountable for driving quality...

Ready to help shape the future of healthcare? Your talent can bring our science to lifeAs a modern employer, we empower you to be yourself, share ideas and work collaboratively**_Manager QA Operations_**:Job purpose: Act with colleagues of the production team and Primary / Secondary Quality Assurance Team to ensure the continuous supply of vaccines in line...

Site Name: Belgium-WavrePosted Date: May 2 2024About the role:A professional engineer within TRD GMP M&CS who is responsible for the execution and implementation of equipment in vaccines projects, maintenance and automation projects in accordance with agreed deliverables (Quality, EHS, Finance, and Schedule). This person contributes to the liaison...

Site Name: Belgium-WavrePosted Date: Mar **_Specialist QA validation projects PA/IPV_**Job Purpose- _ Built a strong partnership with the MU stakeholders in Validation/Process, Projects and external partners outside MU (central and global functions)_- _ Ensure regulatory compliance and audit readiness of the MU in scope and defend the validation approaches...

Site Name: Belgium-WavrePosted Date: Jun 6 2023Job purpose: In the context of GSK business growth, take responsibility for quality aspects (QA, QC, manufacturing and validation activities) within the groups of MSAT Technical Transfer and External Manufacturing Vaccines. Be accountable from Quality point of view to ensure a successful technical transfer...

Site Name: Belgium-WavrePosted Date: May **_Specialist QA validation _**Job Purpose- _ Built a strong partnership with the MU stakeholders in Validation/Process, Projects and external partners outside MU (central and global functions)_- _ Ensure regulatory compliance and audit readiness of the MU in scope and defend the validation approaches and decisions...

Job Description Your mission : MANAGE BUSINESS IT TEAM WITHIN A GMP ENVIRONMENT People management (support, evaluation, hiring) Organization of the team and assignment of the projects/tasks to the member of the team Participation to customer audit and authorities' inspections Define priorities in collaboration with operational managers. MANAGE...

Site Name: Belgium-WavrePosted Date: May 7 2024Key Responsibilities: Responsible for activities and resources engaged in the production process- and for their continuous optimization. Coordinates manpower trajects, resources and skills. Evaluates capacities (employees and machines) necessary to the completion of the production plan. Supervises/ manages day...

Site Name: Belgium-WavrePosted Date: Jul 5 2023_ Specialist, Operational QA, Live Viral Vaccines_:An operational role, with the responsibility for quality oversight of the manufacturing of live viral vaccines.In this role you will: Ensure regulatory compliance of operations and escalate major quality issues and/or compliance gaps Evaluate product impact and...

Site Name: Belgium-WavrePosted Date: Mar _ First Line Leader - Night Shift_:Job purpose:As a _First Line Leader - Night Shif,_ you will be responsible for the operations of a production plant within a production site:Responsible for activities and resources engaged in the production process and for their continuous optimization Coordination of manpower...

In het kortwavrebediende, freelancer40 uur per week Joachim CemolinTalent Acquisition Specialist Life Sciences- Quality Assurance Officer: Pharma & Sciences Quality & Compliance Develop and implement QA processes and standards following authorities guidelines and GMP Review product specs, batch records, and quality test data to maintain our client's high...

Site Name: Belgium-Wavre, Durham Blackwell Street, StevenagePosted Date: May 3 2023About the role:As a Associate Director, Third-Party Programme Management, CQA, you will be expected to deliver independent quality oversight and management to GSK R&D as a valued partner acting as the single point of accountability for one or more clinical development...

Please note that this is a 6-months contract. Job purpose: European cGMPs (Eudralex vol4) define that the purpose of controlling batch release is to ensure that the batch has been manufactured and checked in accordance with the requirements of its marketing authorization, the principles and guidelines of Good Manufacturing Practice and any other...

Site Name: Belgium-Wavre, GSK Tres Cantos, MadridPosted Date: Mar _ QA Manager External Manufacturing - CMO _: Job purpose: _ Take responsibility for the Contract Manufacturer Quality oversight quality aspects (QA and QC) within the group of Tech Transfer / External Manufacturing Operations. Ensure the release of the commercial batches in compliance with the...

**Site Name**: Belgium-Wavre**Posted Date**: Nov En tant que ** QA**, vous êtes en charge de l'assurance de la qualité de la documentation GMP, de la revue qualité et du travail de terrain.**Vos responsabilités sont**:- Assurance de la qualité des batch records ainsi que leur clôture dans les délais- Assurance du bon suivi des procédures sur le...