The Environment Agency are recruiting environment and science professionals of the future, onto our (approximately) four-year Environment and Science Graduate Training Scheme (ES-GTS). ...
Contract: Full time/6 month fixed term contract.Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients....
Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.We are currently looking for an experienced Seni...
Key Words: Analytical Development | Method Development | Assay Development | MDV | Protein Characterisation | Product Characterisation | Protein Analysis | AAV | Viral Vector | Gene Therapy | GMP | QC | Quality Control | CMC | Biologics | Biopharmaceutical | C> | ATMP | Analytical Chemist | Senio...
You’re either a Graduate or someone with 12 months experience with transferable skills. Whilst we are ideally looking someone who has recently graduated or about to, if you don’t fall into that category but think Levin is the place for you, we’d love to hear from you. ...
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At Pareto, we have range of entry level graduate schemes where we deliver award winning training and you reap the benefits. Fact Number 2 – There is an abundance of fantastic graduate opportunities in Manchester, and a candidate driven marketplace means that you’re in a stronger position than eve...
Our award winning, internationally renowned client need a number of ambitious, commercially astute graduates for the next intake of their graduate programme!. The scheme will enable rotation across differing arms of the business, allowing you the room to work out how and where you want to progres...
Experience in submissions using MHRA and CESP Portals. Monday to Friday. Full Time
Play a figurehead role in managing regulatory agency inspections from MHRA, EMA, and FDA. * Oversee a global electronic Quality Management System along with managing a network of CMOs. * Lead Quality ...
... MHRA), the role will expose you to all parts of quality management within the business.In the initial phase, the Quality Manager will be a standalone role, so you need to be prepared to roll your ...
Ensure compliance to the relevant company SOP & current MHRA & EU GDP requirement * Drive sustainable compliance to current global quality requirements * Participate in resolving quality matters with ...
... MHRA | PSUR
... MHRA, audit, release
Understand the role of the MHRA (and other competent authorities) in the licensing of medicines, the risk-based inspection process, the role of the enforcement group, the Inspection Action (IAG) and ...
Up-to-date knowledge of the ABPI, PAGB codes, MHRA and other relevant international regulatory bodies * Understanding of the NHS/ international health systems and broader health environment
EU and UK product labelling approval and compliance with the MA approval activities. * interact with the MHRA and any EU UK Regulatory Authority. Ensuring that regulatory processes are completed and ...
Knowledge of GMP and GDP and MHRA Guidance Note 14 * Practical experience in GxP Supply Chain, Production and Quality Assurance * Pro-active and solutions-driven, with the ability to work to strict ...
Experience with submissions to the MHRA is essential * Bachelor's degree or equivalent in a relevant scientific subject
Previous involvement in a regulated laboratory atmosphere (like MHRA GCP for laboratories, GLP, or GMP). * Proficiency in operating and resolving issues with ELISA analytical systems. * BSc Science ...
Ensure compliance to the relevant company SOP & current MHRA & EU GDP requirement * Participate in resolving quality matters with contract manufacturers * Participate in resolving supply chain ...
... MHRA/GCP/ICH requirements. * Prepare Investigational Product Review Forms (IPRFs) and submit them to WEP Clinical Regulatory team. * Support preparation of study files based on project scope ...