11/06/2024 | Fulltime | CV-LibrarySenior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team members deliver Global RA initiatives in designated
Save for laterRegister your CV11/06/2024 | Fulltime | Brimscombe | CV-LibraryEnsuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk
Save for laterRegister your CV11/06/2024 | Fulltime | Cambridge | CV-LibraryTo implementation of novel methods into project work. Maintain an electronic lab note-book and records of experiments, write protocols and assist in the preparation of standard operating procedures and risk assessments. To be considered for the position you should have the following PhD in a relevant life science
Save for laterRegister your CV11/06/2024 | Fulltime | Lydbrook | CV-LibraryEnsuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk
Save for laterRegister your CV11/06/2024 | Fulltime | CV-LibrarySenior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team members deliver Global RA initiatives in designated
Save for laterRegister your CV11/06/2024 | Fulltime | Minchinhampton | CV-LibraryEnsuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk
Save for laterRegister your CV11/06/2024 | Fulltime | CV-LibraryEnsuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk
Save for laterRegister your CV11/06/2024 | Fulltime | Stoke-on-Trent | CV-Library | £45,000 - £60,000 / Year Testing processes. Providing guidance to program management on risk management. Knowledge of Linux based systems and databases Professional certification such as Six Sigma, Quality Engineer, or Quality Auditor Bachelor's degree in Computer Science or relevant Engineering degree 5+ years of experience
Save for laterRegister your CV11/06/2024 | Fulltime | CV-LibraryEnsuring all aspects of analytical development and validation are delivered to the required standard of science, quality and regulatory compliance in accordance with agreed timelines. Assist with and ensure Quality Management System processes such as Change Controls, Deviations, CAPAs and Quality Risk
Save for laterRegister your CV11/06/2024 | Fulltime | CV-LibraryPartners, and our employees. The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team
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