Quality Assurance Pharma Jobs in Europe
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Top Job
The Director of Regulatory Affairs for RAQA is responsible for development and coordination of all harmonized regulatory requirements. Leads, strategizes, develops and implements...
Posted 8 days ago Deadline 31 August -
Top Job
In your new role, you are the primary Quality Assurance contact for our contract manufacturers, contract laboratories or service providers in their day-to-day business to ensure...
Posted 29 days ago -
Develop and set strategic direction for global quality organization including quality systems, quality assurance, supplier quality, design assurance and documentation control. Lead...
Posted 1 day ago -
Support the release and stability sample testing and implementation in collaboration with counterparts in the U.S. Furthermore, the job holder contributes proactively to regulatory...
Posted 2 days ago -
In your new role you are responsible for successful mammalian cell culture (upstream) process transfers of early stage biological (CMC I) and late stage biological (CMC II)...
Posted 2 days ago -
Jobs like this to
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The Clinical Team Manager (CTM) provides operational expertise and leadership in the planning, implementation and management of clinical trials through all periods of trial...
Posted 6 days ago -
The Senior Clinical Research Associate is responsible for the monitoring of clinical trials and tracking of study progress, thereby contributing to the overall management of...
Posted 7 days ago -
Optimize a QA unit that can support the organization in late stage clinical trials and market authorization; Set global GCP goals and monitor the progress; Lead and extend a local...
Posted 8 days ago -
You will be managing and developing the QA Operations department to meet regulations and business needs. You will also be a member of the Site Leadership Team and represents QA and...
Posted 12 days ago -
The Senior Manager of GxP Compliance Strategy will support the management of Health Authorities Regulatory Inspections including but not limited to, participation in the on-going...
Posted 23 days ago -
CEP Revisions’ Team Supervisor
Council of Europe - European Directorate for the Quality of Medicines & Healthcare (CoE EDQM)Strasbourg, FranceReviewing assessment reports related to CEP revision and renewal dossiers drafted by junior scientific assistants, participating in scientific decisions taken on dossiers to ensure...
Posted 26 days ago Deadline 26 August -
Moderna is seeking an AD/D External Quality Control to oversee Quality Control (QC) testing including in-process, release, and stability in support of contract manufacturing and...
Posted 27 days ago -
Organises and oversees the local Quality management system of the “exploitant” (commercial affiliate) in line with global policies and national requirements in accordance with...
Posted 28 days ago -
As a Lead Data Manager you will be accepting this exciting opportunity to lead interesting, mainly early phase clinical trials. As a key member of the clinical study team, you will...
Posted 34 days ago -
This is a leadership role responsible to manage the Quality assurance activities of the new bio-manufacturing plant in line with cGMP regulations for clinical and commercial supply...
Posted 34 days ago -
QA handling, review and support of Quality Management System (QMS) documents and Corrective and Preventive Actions (CAPA), handle QA, approval of changes, quality agreements and...
Posted 34 days ago -
The Clinical Research Associate will identify, select, initiate and close-out appropriate investigational sites for clinical studies. The successful candidate(s) will monitor these...
Posted 36 days ago -
As a Quality System Manager you are the Global Quality System process owner, you develop and implement Quality System strategy and architecture for the company and ensure...
Posted 37 days ago -
This role has a specific focus on maintaining QMS systems and supplier quality audits of non-S+N companies. Works closely with non-S+N and S+N Franchise Regulatory across three...
Posted 40 days ago -
The (Senior) Medical Director provides leadership to the global medical function including medical monitoring. This position collaborates with Medical Affairs Leadership on the...
Posted 41 days ago -
The Senior Director of Quality is responsible for setting the strategic direction, properly staffing and maintaining the Quality Management Systems (QMS) to assure the site is...
Posted 41 days ago -
Assume responsibility for all aspects and processes related to drug safety, including the collection and processing of safety relevant data in clinical studies, signal detection,...
Posted 43 days ago -
Lead the global team clinical team (including CRA's) on projects, providing the team with direction guidance. Build in all necessary project training built in for assigned clinical...
Posted 43 days ago -
My client is looking for an experienced and motivated candidate for the position of Project Manager – Technology Transfer within their global medical diagnostics and therapeutics...
Posted 49 days ago -
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OctapharmaLachen, SwitzerlandPosted 19 days ago
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BioNTechIdar-Oberstein, GermanyPosted 37 days ago
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