REGULATORY AND PHARMACOVIGILANCE PRODUCT jobs in ENGLAND, United Kingdom

.com and follow @JazzPharma on Twitter. Brief Description: To lead Jazz's Pharmacovigilance QA (GvP) function to assure regulatory... therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage...

legislation Maintenance and communication of electronic regulatory file information for each product. Supporting application... and packaging records review and update Regulatory files compliance checks Pharmacovigilance (PV) Responsibilities...

but not limited to Pharmacovigilance and Patient Safety, Regulatory Affairs and Medical Affairs to ensure optimal QA oversight... and development for the product’s lifecycle to achieve product realization and accelerate access to innovative therapies and products...

but not limited to Pharmacovigilance and Patient Safety, Regulatory Affairs and Medical Affairs to ensure optimal QA oversight... and development for the product's lifecycle to achieve product realization and accelerate access to innovative therapies and products...

strategies to maximize regulatory and pharmacovigilance success. · Sound knowledge of requirements of MA Transfer in EU... activities are carried out in Regulatory and Pharmacovigilance. · Drive all pre-submission meetings including inputting...

and strategically leading cross-functional matrix teams responsible for product safety and benefit risk oversight. The MSO will report...), Qualified Person for Pharmacovigilance (QPPV), Senior Management, Health Authorities (HA), prescribers and/or patients. In...

and strategically leading cross-functional matrix teams responsible for product safety and benefit risk oversight. The MSO will report...), Qualified Person for Pharmacovigilance (QPPV), Senior Management, Health Authorities (HA), prescribers and/or patients. In...

local and global submissions Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA...SRG are partnered with a pharmaceutical organisation who are seeking a Product Surveillance Reporting Analyst...

Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for submissions and escalates requests...Product Surveillance Reporting Analyst 12 months £17.96 p/h Marlow - hybrid (3 days on site) SRG are partnered...

submissions, responses to regulatory agency inquiries, pharmacovigilance (PV) processes and projects, and PV or other audits... into product development and lifecycle management as well as perform or oversee other advanced MSS activities...

function within Bicycle Therapeutics provides clinical safety and pharmacovigilance support to medicines across life cycle... for the assigned compounds within the organization. Responsible for the implementation and the management of pharmacovigilance...

projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. We encourage you to closely follow... and responsibilities are likely to include: You will provide medico-scientific and clinical strategic leadership for assigned product...

activities of an international portfolio of subcontractors, diverse and high-tech product portfolio As a Quality expert... necessary for the manufacture and release of batches such as Product Specification Files, Master Batch Records, Supply Chain...

safety signals. Contribute to the strategy and review of safety assessments and for signals or issues (including product... quality) or in response to Regulatory Authority requests. Lead the collection of material for periodic reports e.g. DSUR...

of experience in the Regulatory Affairs & Pharmacovigilance · Proficiency in the use of MS Office suite (Excel, PowerPoint...Job Title: Pharmacovigilance Co-ordinator Employment Type: Permanent Position Salary: £35,000 per annum Location...

Brands req? No Keywords Medicine, Regulatory, Manager Latitude,longitude 1 52.927182,-1.183948 Function Product...Job Description Medicine Regulatory Manager Vacancy closing date: 22nd May 2024 Recruitment Partner: Laura Taylor...

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...