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Pharmaceuticals
Senior Pharmacovigilance Officer
Northamptonshire
DBS Not Required
Senior Pharmacovigilance Officer - Pharmaceuticals - Midlands
A fan...
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.
Chemicals~Household
Regulatory Affairs Consultant – Biocides -(Remote)
£50,000
Tyne and Wear
DBS Not Required
Regulatory Affairs Consultant – Biocides – Remote
An independent regulatory...
Regulatory Affairs Consultant – Biocides – Remote
An independent regulatory consultancy is looking to hire a Biocides Regulatory specialist to their team. The business provides regulatory services to all sectors of the chemicals industry. They have a UK and EU presence, offer flexible and remote/hybrid working for experienced regulatory specialists along with an excellent benefits package.
Responsibilities:Will act as biocide regulatory affairs expert for the business (EU AND UK BPR)Responsible for successful management and delivery of projects to selected companiesOffering regulatory advice and deliverablesProvide scientific and technical input into processesAct as a client liaison for relevant projectsTake part in training / L&D continuing their professional developmentProvide business development strategies
Minimum essential requirement:You must have Industry or consultancy experience supporting biocidal active substance and product registrations in the EU and/or UK
To find out more about this Biocides Regulatory Specialist role please send a word version of your CV!
An independent regulatory consultancy is looking to hire a Biocides Regulatory specialist to their team. The business provides regulatory services to all sectors of the chemicals industry. They have a UK and EU presence, offer flexible and remote/hybrid working for experienced regulatory specialists along with an excellent benefits package.
Responsibilities:Will act as biocide regulatory affairs expert for the business (EU AND UK BPR)Responsible for successful management and delivery of projects to selected companiesOffering regulatory advice and deliverablesProvide scientific and technical input into processesAct as a client liaison for relevant projectsTake part in training / L&D continuing their professional developmentProvide business development strategies
Minimum essential requirement:You must have Industry or consultancy experience supporting biocidal active substance and product registrations in the EU and/or UK
To find out more about this Biocides Regulatory Specialist role please send a word version of your CV!