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Pharmacovigilance jobs in Milton keynes

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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...
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...
Complaints Intake Analyst 27451 MARLOW, BUCKINGHAMSHIRE, SL7 ...Regulatory Affairs and Pharmacovigilance Supports more complex complaints that are escalated Serve as a Subject Matter Expert for a designated product(s) within the team when required Where applicable, decide whether a replacement, credit, or warranty claim is warranted, and notify the...
Looking for Pharmacovigilance jobs in Milton Keynes? Top Salaries! Full time, part time and contract. MILTON KEYNES Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.

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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...
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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 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...
Senior Pharmacovigilance Manager 41680 WEYBRIDGE, SURREY, WEYBRIDGE, SURREY Hobson Prior is seeking a Senior Pharmacovigilance Manager. The successful candidate will maintain the overall safety profiles and any emerging safety concerns concerning the pharmaceutical products. This role is crucial in managing all pharmacovigilance risk management issues and acting as the UK...
Clinical Trial Specialist Apprentice FARNBOROUGH, HAMPSHIRE, FARNBOROUGH, HAMPSHIRE ...Up Data Management Pharmacovigilance These are office based departments, not lab or hospital based. Qualifications What do I need to have/demonstrate to be eligible? Minimum 5 GCSEs grades 9 to 4 (A to C) including Maths and English language Have/be predicted to achieve 80 UCAS points...
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...
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...
! 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...
Pharmacovigilance Co-ordinator £35000/annum Excellent Benefits DARTFORD, KENT, DA1 Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator. Job Description: Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. Liaise...
Senior Manager Regulatory Affairs & Pharmacovigilance 47145 DARTFORD, KENT, DA1 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...
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