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Automation Project Manager - Global Pharma - Perm
WATFORD, 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...
Automation Project Manager - Global Pharma - Perm
WATFORD, HERTFORDSHIRE, EAST ANGLIA
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of...
Automation Project Manager
HERTFORDSHIRE, 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...
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Automation Project Manager
HERTFORDSHIRE, EAST ANGLIA
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of...
We've expanded the search to "East Anglia" to find more jobs with all your keywords
Qualified Person, Pharmacovigilance (QPPV)
LUTON, ENGLAND, UNITED KINGDOM
...maintain the company's Pharmacovigilance system. Being the main point of contact for MHRA competent authority. Responsibilities: Acting as the single point of contact for MHRA competent authority on a 24-hour basis. Ensuring the structure and performance of the pharmacovigilance system complies...
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Associate Director, GCP and GLP Quality Assurance Cambridge, MA, United States Posted on 08/11/[...]
£80 - 100
CAMBRIDGE
...Drug Safety & Pharmacovigilance, and Regulatory teams, contribute to the design and implementation of a risk-based clinical Quality Assurance management system. br /li li Review and approve CRO quality events and CAPA, as appropriate. br /li li Identify QA and compliance related...
Senior Manager, Quality
ABINGTON PIGOTTS, EAST ANGLIA
...Data Management, Pharmacovigilance, etc.) based on analysis and interpretation of applicable regulations. Identify and partner with key collaborator functions and business partners as appropriate. /li li Assist development team business partners with development and documentation of CAPAs...
We've expanded the search to "England" to find more jobs with all your keywords
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...
QPPV office and Alliance Management
GREATER LONDON, ENGLAND, UNITED KINGDOM
Passionate about transforming lives? Ready to drive innovation in Research & Development? We're on a mission to revolutionise patient care and need your expertise to make it happen. QPPV Office & Alliance Manager (f/m/d) What You'll Do: Lead global Pharmacovigilance system with finesse...
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...
Senior Regulatory Affairs & PV Manager
GREATER LONDON, ENGLAND, UNITED KINGDOM
...maximize regulatory and pharmacovigilance success. knowledge of requirements of MA Transfer in EU territories, which includes requirements of notarization and translations. a team of 4 to ensure day-to-day activities are carried out in Regulatory and Pharmacovigilance. all pre-submission meetings...
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...
Environment, Health and Safety Manager
MIDDLETON, 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...
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...
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...
Computer System Compliance Auditor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice...
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