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Senior Manager Regulatory Affairs & Pharmacovigilance
not provided
DARTFORD, KENT, SOUTH EAST, UK
Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Senior Manager Regulatory Affairs & Pharmacovigilance. Job Requirements: Define, develop, and leads regional strategies to maximise regulatory and pharmacovigilance success...
Global Quality Manager
WINDSOR, ENGLAND, UNITED KINGDOM
Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management. The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the...
Global Quality Manager
WINDSOR, SOUTH EAST ENGLAND
p Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management. /p p br /p p The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the...
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Manager, Global Aggregate Reports quality and compliance
BERKSHIRE, ENGLAND, UNITED KINGDOM
...of new and evolving pharmacovigilance legislation within the GRIP process. Coordinates the Aggregate Reports Quality Review Board and overseeing Aggregate report KPIs across CSL business units. The authoring of high quality regulatory required aggregate reports including scientific analysis...
Head of Global Safety Data Integration and Literature (UK)
£80 - 100
SLOUGH
...team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices. /p p b About the role: /b /p p You will play a pivotal role in oversight and implementation of new and improved solutions to...
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Product Surveillance Reporting Analyst
MARLOW, ENGLAND, GB
...internal teams such as pharmacovigilance, local in-country teams, and the device quality assurance team to ensure the appropriate and accurate reporting of complaints. Responsibilities: Decision maker for all reportability decisions Lead for all vigilance reporting, including local and global...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new processes necessary to deliver compliance with European and local legislation. You will support the European Head of Pharmacovigilance and...
Regulatory Affairs Role
HAMPSHIRE, ENGLAND, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
Production Technician
MILTON KEYNES, ENGLAND, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
Scientist - Bioanalytics/Mass Spectrometry
READING, ENGLAND, UNITED KINGDOM
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
Senior Regulatory Affairs & PV Manager
LONDON, SOUTH EAST ENGLAND
...maximize regulatory and pharmacovigilance success. /li li knowledge of requirements of MA Transfer in EU territories, which includes requirements of notarization and translations. /li li a team of 4 to ensure day-to-day activities are carried out in Regulatory and Pharmacovigilance. /li li all...
Product Surveillance Reporting Analyst
MARLOW, SOUTH EAST ENGLAND
...internal teams such as pharmacovigilance, local in-country teams, and the device quality assurance team to ensure the appropriate and accurate reporting of complaints. /p p b Responsibilities: /b /p p • Decision maker for all reportability decisions /p p • Lead for all vigilance...
Regulatory Affairs Manager- Alvita
WOKING, SOUTH EAST ENGLAND
...Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new processes necessary to deliver compliance with European and local legislation. /li li You will support the European Head of...
Regulatory Affairs Role
HAMPSHIRE, SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates...
Portfolio Marketing Manager - Global Company
ANDOVER, SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates...
Car Fleet Manager
LONDON (HAYES), SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates...
! Regulatory Affairs Manager - Remote/hybrid in Uxbridge - Global Biotech !
LONDON (UXBRIDGE), SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates...
! RBDS Supervisor based in Andover - Leading Chemical manufacturing!
ANDOVER, SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates...
Production Technician
MILTON KEYNES, SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates...
Scientist - Bioanalytics/Mass Spectrometry
READING, SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates...
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