| Job alert | Jobs 1 - 10 of 16 |
Senior Clinical Trial Manager Oncology
Gilead Science
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Uxbridge, Greater London, United Kingdom
... management level Previous monitoring experience is desired but not essential for the role Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable Must be able to ... - Apr 18
Medical Device Compliance Manager
InterSystems
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Windsor, Windsor and Maidenhead, SL4 1QT, United Kingdom
As a Medical Device Compliance Manager, you will play a critical role in maintaining and enhancing the compliance standards for our medical devices, with a particular focus on software, in accordance with MDR, FDA, and DCB 0129 requirements. You ... - Apr 10
IS Licensed Animal Technician
Charles River Laboratories
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Ridge, Hertfordshire, EN6 3LD, United Kingdom
... We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in ... - Apr 23
Technical Specialist (IS)
Charles River Laboratories
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Ridge, Hertfordshire, EN6 3LD, United Kingdom
... We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in ... - Apr 22
Associate BD Manager RMS - Southern UK
Charles River Laboratories
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Ridge, Hertfordshire, EN6 3LD, United Kingdom
... We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in ... - Apr 22
Director EU, Regulatory & Scientific Policy (all genders)
Merck
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Feltham, Greater London, TW14 8HA, United Kingdom
... Who you are 10 years of experience in drug development/regulatory in the pharmaceutical industry Knowledge of drug development process EMA/EC/FDA/ICH regulations and guidelines Understanding/experience in policy development and implementation ... - May 01
Lead (Clinical) Data Manager
Indivior
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London, Greater London, United Kingdom
... Working knowledge of ICH, FDA, CFR, GCP, HIPAA, GCDMP regulations and guidelines. Working knowledge of and experience implementing CDISC CDASH / SDTM / ADaM standards. COMPETENCIES/CONDUCT In addition to the minimum qualifications, the employee will ... - Apr 17
Assistant Production Manager
Belazu
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Greenford, Greater London, United Kingdom
... Possess good knowledge of food safety regulations (e.g., HACCP, FDA, GMP) ️ Lead by example and can demonstrate success in helping your team step up in optimising production processes effectively, motivating your team to collaboratively ... - Apr 22
Audit Management Senior Manager, month FTC
Vertex
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Westminster, Greater London, W2 1HB, United Kingdom
... 21 CFR Parts 210/211/610/820/11/1271 and applicable FDA guidelines, ICH guidelines, EudraLex - Volume 4 - Good Manufacturing Practice (GMP) guidelines / Annexes, and applicable international equivalents Deviation / OOS Investigations, Root Cause ... - Apr 05
Post Market Surveillance Lead
Philips
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Farnborough, Hampshire, United Kingdom
... Background /Experience with global medical device regulations, requirements, and standards such as ISO13485, ISO9001, MDD, European Medical Device Regulation (MDR), FDA QSR . Ability to move strategy into action, drive decisions while effectively ... - Apr 25