18/09/2024 | Fulltime | | United Kingdom | CV-LibraryOr aligned working experience Practical experience (8+ years) in QA and/or Validation roles within the Pharmaceutical and or Medical Devices industry Managerial experience or Supervisory responsibilities Excellent knowledge and application of GMP and Pharmaceutical regulatory requirements Expert knowledge
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-LibraryThe value of Mundipharma's assets, ensuring internal alignment and successful external stakeholder engagement to enable patient access to medicines and commercial success. As a role model, this leader adheres to and promotes Mundipharma's value-based pricing mindset. Other responsibilities of the role
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-Library | €14 - €18 / Hour And occasional customer meetings. The Candidate The ideal Marketing Coordinator will have - 1-2 years of experience in a similar role. - Experience in a healthcare, hospital, or medical setting is ideal; experience in a regulated industry is beneficial. - Proficiency with MS Office and Salesforce
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-LibraryOr aligned working experience Practical experience (8+ years) in QA and/or Validation roles within the Pharmaceutical and or Medical Devices industry Managerial experience or Supervisory responsibilities Excellent knowledge and application of GMP and Pharmaceutical regulatory requirements Expert knowledge
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-Library | €16 - €27 / Hour Quality Specialist. This role will expose you to the full range of investigational medicinal products in the company development pipeline, from simple small molecules through to complex immunotherapy treatments, and a chance to make a real difference to patients receiving these lifesaving and life
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-Library | €28,000 - €34,000 / Year And appropriately challenge To safeguard and provide consistency and stability To provide advocacy and act with sensitivity Administer medication where needed Maintain adequate records and undertake site risk assessments Write reports and care planning documentation with the use of IT skills Provide stimulating
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-LibraryOr similar or aligned working experience Practical experience (8+ years) in QA and/or Validation roles within the Pharmaceutical and or Medical Devices industry Managerial experience or Supervisory responsibilities Excellent knowledge and application of GMP and Pharmaceutical regulatory requirements Expert
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-LibraryThe value of Mundipharma's assets, ensuring internal alignment and successful external stakeholder engagement to enable patient access to medicines and commercial success. As a role model, this leader adheres to and promotes Mundipharma's value-based pricing mindset. Other responsibilities of the role
Save for later18/09/2024 | Fulltime | | United Kingdom | CV-LibraryWith families, healthcare professionals and other stakeholders to ensure that the best care plans are created and delivered Administering and recording medication Carrying out risk assessments Working alongside care assistants to support residents with daily needs, ensuring residents remain as active
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