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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 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...
Program Manager (Clinical Trials/Managed Access)
WEYBRIDGE, ENGLAND, UNITED KINGDOM
...as it relates to pharmacovigilance workflows, order processing, logistics, regulatory scoping, client set-up documents, etc Be responsible for program related updates, implementation of such updates via defined change control processes and ensuring relevant teams are trained as appropriate...
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Associate Director, Pharmacovigilance QA - Home Based / Remote
OXFORD, ENGLAND, GB
...To lead Jazz s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quality strategy, as...
Senior Clinical Quality Assurance Specialist (Remote / Home Based)
OXFORD, ENGLAND, GB
...Trials, including Pharmacovigilance activities and quality vendor management. CQA Quality Lead for Clinical Quality Assurance to support Study teams, providing quality support and regulatory requirements advice/guidance for multiple clinical studies/trials. Create and Manage Study Quality...
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Manager, Quality and Compliance - 8 months FTC
OXFORD, ENGLAND, GB
...Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations, industry standards, Jazz policies, procedures and quality standards in support of the Quality Management System within the...
Senior Manager Pharmacology, Neuroscience (Remote)
OXFORD, ENGLAND, GB
...to regulatory, pharmacovigilance and medical affairs documents as required to meet corporate needs Contribute to Function and/or Programme (pre-DP0) or Project (post-DP0) Teams as determined within the governance matrix structure Responsible for maintaining own cGxP and H&S knowledge...
Senior Administrative Assistant - R&D
OXFORD, ENGLAND, GB
...with prior regulatory/pharmacovigilance support as a key advantage Ability to multi-task and work in a global, fast-paced environment, often under tight deadlines Ability to prioritize workload and manage multiple projects simultaneously, with strong attention to detail Experience working in an...
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...
Pharmacovigilance Manager
WINDSOR, ENGLAND, UNITED KINGDOM
Job Title: Quality Manager, Global Quality Management Location: UK (preferably located near Windsor) Are you a Pharmacovigilance professional with a keen eye for quality management? Do you possess experience in audits, inspections, and CAPA management, and aspire to transition into a broader...
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...
Product Surveillance Reporting Analyst
MARLOW, ENGLAND, UNITED KINGDOM
...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...
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...
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...
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...
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...
GCSP Regions Head of Europe
WEST SUSSEX, ENGLAND, UNITED KINGDOM
The GCSP Regions Head of Europe is a leadership position for providing end-to-end pharmacovigilance (PV) strategic insight and operational oversight for CSL enterprise affiliates and guiding PV operations in the Affiliates. The role directly manages personnel including Regions Territory Managers...
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...
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