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PV Manager and Deputy QPPV

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Hays

2021-12-03 22:00:05

Job location Greenford, Greater London, United Kingdom

Job type: fulltime

Job industry: Healthcare & Medical

Job description

Drug Safety Manager and Deputy QPPV for a global pharmaceutical company

A well-established, exciting and global pharmaceutical company based in West London are now searching for a PV Manager and Deputy QPPV to join their small and close-knit team in the UK. They are market leaders in Semi-Synthetic Penicillin's and as well as this, they have a presence in exciting therapeutic areas such as neurosciences, cardiovascular, anti-retrovirals, gastroenterology and many more.

This is an exciting long-term prospect as the company keeps growing, providing excellent exposure on a global scale in a collaborative, diverse and like-minded environment. You will be provided with plenty of support and they company are renowned for their diversity, scale, leadership, patient focus and operational excellence. As well as this they have sustainability at their forefront and have put in clear efforts to benefit the communities they work with.

This an opportunity provides great variety and you will be reporting directly into the UK QPPV. Your main responsibilities will include, but are not limited to:
- Acting as Deputy QPPV and coordinating with the QPPV to ensure adequate processes are in place to ensure compliance of the PV system
- Change Management of local PV systems and processes
- Managing service providers for UK & Ireland
- Ensuring medical information activities are complemented in a timely manner
- Ensuring all ADRs are reported to Global and EU PV Department, all enquiries are tracked, responsibility for investigation, conclusion and responses to patients
- Support the submissions of PSURs, RMPs, ACOs or any other PV documents
- Tracking all RMMs
- Management of local Deviations and CAPAs for all designated PV activities
- Execution of SDEAs
- Ensuring compliance and preparation of monthly PV Compliance reports
- Participation in organizational development projects (including EU wide projects)

What do you need?
- A strong background in pharmacovigilance, 5 years + or equivalent
- Knowledge of post-marketing PV regulations
- Ideally experience in generic pharmaceuticals
- Excellent communication skills
- Proven ability to working independently, prioritise tasks and influencing others to achieve results
- Commitment to go to the office

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

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