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Pharmaceuticals
Senior Pharmacovigilance Officer
Northamptonshire
DBS Not Required
Senior Pharmacovigilance Officer - Pharmaceuticals - Midlands
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Senior Pharmacovigilance Officer - Pharmaceuticals - Midlands
A fantastic position has become available as a Senior Pharmacovigilance Officer. This company has doubled in size since its inception, and it will be a great opportunity for a Senior PV Officer to progress their career even further. As a Pharmacovigilance Officer, you will be required to review CAPAs; Maintain SOPs and review documentation, surrounding the adverse effects of released drug product.
As a Senior Pharmacovigilance Officer, you will be required to:
Provide first inspection of individual case safety reports (ICSRs)
Conduct Document Control, surrounding the adverse effects of a released drug product.
Maintain the SOPs.
Review and Implement CAPAs.
Conduct Change Controls.
Utilise their own unique QMS.
Required Skills
Documentation review.
Knowledge and experience within the pharmaceutical industry.
Strong communicative skills.
Ability to meet deadlines and manage workloads.
3 + Years working within pharmaceutical pharmacovigilance (UK Market)
Desirable Skills (Not Compulsory)
A Degree within a Chemistry/Scientific background.
Demonstrable experience working within a QA or PV Environment.
Have great knowledge and understanding of GMP/GDP.
Supervision experience
PLEASE NOTE: This company does not have the ability to provide Sponsorship. You MUST have a Full & Permanent right to work in the UK.
Please Contact Aidan Stanley at Science Solutions Recruitment.
A fantastic position has become available as a Senior Pharmacovigilance Officer. This company has doubled in size since its inception, and it will be a great opportunity for a Senior PV Officer to progress their career even further. As a Pharmacovigilance Officer, you will be required to review CAPAs; Maintain SOPs and review documentation, surrounding the adverse effects of released drug product.
As a Senior Pharmacovigilance Officer, you will be required to:
Provide first inspection of individual case safety reports (ICSRs)
Conduct Document Control, surrounding the adverse effects of a released drug product.
Maintain the SOPs.
Review and Implement CAPAs.
Conduct Change Controls.
Utilise their own unique QMS.
Required Skills
Documentation review.
Knowledge and experience within the pharmaceutical industry.
Strong communicative skills.
Ability to meet deadlines and manage workloads.
3 + Years working within pharmaceutical pharmacovigilance (UK Market)
Desirable Skills (Not Compulsory)
A Degree within a Chemistry/Scientific background.
Demonstrable experience working within a QA or PV Environment.
Have great knowledge and understanding of GMP/GDP.
Supervision experience
PLEASE NOTE: This company does not have the ability to provide Sponsorship. You MUST have a Full & Permanent right to work in the UK.
Please Contact Aidan Stanley at Science Solutions Recruitment.