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Pharmacovigilance Auditor
, , UNITED KINGDOM
...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
PV Physician (Director) - Remote
LONDON, ENGLAND, UNITED KINGDOM
Hobson Prior is currently seeking a PV Physician (Director Level) for a remote position located in either London or Paris. The successful candidate will be responsible for providing medical and scientific support to pharmacovigilance in accordance with applicable regulatory guidelines/requirements...
Pharmacovigilance Auditor
UNITED KINGDOM, UNITED KINGDOM
...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
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Manager, Global Aggregate Reports quality and compliance
BERKSHIRE, ENGLAND, UNITED KINGDOM
The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a...
Counsel, PV & Quality, Legal Global Medical Ops
£100 - 125
LONDON
...support in areas of pharmacovigilance and quality assurance (both R&D and PV) for projects of a lower complexity, using a developing, working knowledge of relevant law and the relevant science. The role can work on matters of higher complexity with the direction and supervision of their...
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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...
Clinical Safety Scientist
£0 - £40 per hour , GBP
BRENTFORD
...Conducting routine pharmacovigilance activities, signal detection/evaluation and leading authoring of key regulatory documents (e.g. DSURs, EU RMPs and PBRERs). Ensuring that all safety documentation is accurate & available to meet global compliance & regulatory requirements. Your Background...
Pharmacovigilance Director of Projects (Europe, USA or Canada)
, , UNITED KINGDOM
We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information...
Quality Specialist
UNITED KINGDOM, , UNITED KINGDOM
...solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Opportunity The Quality...
Senior Drug Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...studies, ensuring compliance with international safety reporting requirements. Provide invaluable medical expertise to our Drug Safety and Pharmacovigilance team, supporting both medically trained and non-medical colleagues. Spearhead training and mentoring initiatives, empowering our team...
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
...in place to maintain compliance with the requirements of the Medical Devices Regulation (EU) 2017/745 and the in Vitro Diagnostic Medical Device Regulation (EU) 2017/746, in the context of our obligations as an own brand. You will demonstrate an innovative approach to obtaining market...
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...
Continuous Improvement PMO
, , UNITED KINGDOM
About the company: We are Qinecsa. Trusted partners to global life science companies. We bring together and offer best-in-class pharmacovigilance technology and scientific expertise to connect life science companies to the right safety solutions. Reportum platform Our automated case intake and...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...programs, ensuring compliance with applicable ICH GCP and GLP standards and global regulations. As an integral member of the team tasked with product development, the position serves as a Quality and compliance business partner, engaging with multiple collaborators. The ideal candidate must...
Global Labelling Lead
UNITED KINGDOM, , UNITED KINGDOM
...Maintain labelling compliance Maintain labelling compliance for assigned products ensuring version control and tracking of CDS implementation in relevant company systems Core labelling supporting documentation Oversee preparation of supporting documents for core labelling changes, in...
Senior Regulatory Affairs Officer
, , UNITED KINGDOM
...submissions, ensuring compliance with regulatory requirements. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Affairs Manager will be varied however the key duties and responsibilities are as follows: 1. Oversee dossier compilation and submission for UK and EU markets. 2. Liaise...
! RBDS Supervisor based in Andover - Leading Chemical manufacturing!
, , UNITED KINGDOM
...regulatory compliance and, above all, safety. We must also be able to respond to our customers changing demands and timescales to ensure that the service we provide delivers meaningful value, above and beyond the decontamination itself. Overview of the role: Our UKIE business is...
Environment, Health and Safety Manager
MIDDLETON, ENGLAND, UNITED KINGDOM
...for Legislative Compliance for all health and safety aspects and managing Integrated management systems ie. ISO14001. Main Responsibilities Health & Safety lead for the Middleton site Prime interface for HSE/EA and other Regulatory Authorities Ensure compliance with Environmental...
! Regulatory Affairs Manager - Remote/hybrid in Uxbridge - Global Biotech !
UXBRIDGE, ENGLAND, UNITED KINGDOM
...timely regulatory compliance with above approvals As requested this role may provide management and leadership by supervising one or more other regional regulatory leads and/or support staff (dependent on grade) Responsible for: Advising the GRT on regional considerations in developing...
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