מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Senior Manager - Regulatory Affairs Innovative Medicines Europe ב-United Kingdom והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו Teva. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
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27 jobs found
23.11.2024
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Teva Senior Microbiology Technician United Kingdom, England
Documentation - checking and approval of batch documentation, (Product and starting materials). Ensure a high level of compliance in accordance with CGMP and maintain performance through regular review of data...
Cartridges & Pen Injectors. Pre-filled Syringe & Safety Systems (PFS). Autoinjectors (AI). Supporting the engineering design and development of drug delivery devices at various stages of development, from research, through...
You will develop regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities. Depending on your experience you may also have the opportunity to do...
Leads, manages and performs data mining, exploration, usage of analytical programs/languages to find anomalies within big data and/or develops and deploys enhanced models. Serves as a partner to business leaders...
You will be responsible for statistical aspect of study designs and data analyses for non-clinical projects. You will provide study design input and consultation for clinical endpoint assessments and sample...
Ensure compliance with all disclosure rules and regulations, e.g. SEC Regulation FD. Collaborate with SVP, Head of Investor Relations and the entire IT team to develop and implement investor relations...
Successfully execute the brand strategy to deliver agreed commercial targets in line with business objectives. Work alongside the Marketing Manager to define brand proposition, positioning and targeting on all new...
Documentation - checking and approval of batch documentation, (Product and starting materials). Ensure a high level of compliance in accordance with CGMP and maintain performance through regular review of data...
Are you an experienced in regulatory affairs in the tech industry? Do you want to join one of the world’s leading pharmaceutical companies, Teva in the United Kingdom? Teva is looking for a Senior Manager of Regulatory Affairs for Innovative Medicines Europe to lead regulatory strategy and plans for a portfolio of products across all regions in Europe.
You will be working closely with the cross-functional teams, including the registration and government affairs teams, to ensure that regulatory strategies are developed, implemented and monitored in line with the company’s objectives. You will be responsible for the timely execution of registration activities and negotiate favorable outcomes with multiple European regulatory agencies. In this role, you will also need to keep up-to-date with industry regulations and best practices of the pharmaceutical industry.
This is an exciting role for driven individuals who thrive in a fast-paced environment. The successful candidate will be a proactive and strategic self-starter, with deep regulatory knowledge and advanced communication and collaboration skills. A strong understanding of European regulatory requirements and the ability to identify relevant risks and develop mitigation plans are important skills to have in this role. You should also have financial acumen to effectively manage allocated budgets and to provide proper justifications for needed resources.
If you think you have the required skills and knowledge, and looking for a challenging and rewarding opportunity in the tech industry, then this is the role for you. Sign up for Expoint and apply for the Senior Manager of Regulatory Affairs for Innovative Medicines Europe role today.