Medical Device Vigilance jobs
Sort by: relevance - date
Senior Pharmacovigilance Officer
Urgently neededMilpharm LtdUxbridge UB11 1AF- Sick pay
- Life insurance
- Company pension
- Company events
- On-site parking
- Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
- Assist in ensuring continuous oversight of all PV…
- HologicManchester M23 9HZ
- Company pension
- Proven experience in Scientific or Medical Affairs within the medical device industry, ideally with a focus on surgical devices.
- Quoris3DEnniskillen BT94 1RL
- Maintain and develop full regulatory compliance for medical device manufacturing under ISO 13485 and MHRA guidelines.
- ISO 13485: 1 year (preferred).
View similar jobs with this employerMundipharma Research LimitedCambridge CB2 1NT- Governance & Compliance: Establish and oversee global governance frameworks, ensuring all medical activities uphold the highest ethical and scientific standards…
View similar jobs with this employerMundipharma Research LimitedCambridge CB2 1NT- Governance & Compliance: Establish and oversee global governance frameworks, ensuring all medical activities uphold the highest ethical and scientific standards…
- Medicines and Healthcare Products Regulatory...Remote
- Pay rise
- Childcare
- Annual leave
- Sick pay
- Company pension
- Season ticket loan
- Proven track record of undertaking medical device audits.
- A breadth of understanding and practical experience of modern concepts and practicalities underlying…
- Understanding of software validation and cybersecurity requirements in medical devices.
- Experience supporting Class III medical device submissions or…
- Understanding of software validation and cybersecurity requirements in medical devices.
- Experience supporting Class III medical device submissions or…
View similar jobs with this employerSThreeCambridge- Managing regulatory submissions and dossier preparation for medical devices or pharmaceuticals.
- In-depth knowledge of ISO 13485, IEC 62304 and Class III medical…
View similar jobs with this employerSThreeEdinburgh- Managing regulatory submissions and dossier preparation for medical devices or pharmaceuticals.
- In-depth knowledge of ISO 13485, IEC 62304 and Class III medical…
View similar jobs with this employerSThreeManchester- Managing regulatory submissions and dossier preparation for medical devices or pharmaceuticals.
- In-depth knowledge of ISO 13485, IEC 62304 and Class III medical…
- Ministry of Defence Guard ServiceChivenor
- Employee discount
- Company pension
- Successful candidates will be expected to have a medical.
- Monitor security systems – Operate CCTV, alarms, and communication devices.
- Pay: £32,530.00 per year.
- CSLMaidenhead SL6 8AA
- You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain…
- Understanding of software validation and cybersecurity requirements in medical devices.
- Experience supporting Class III medical device submissions or…
- Managing regulatory submissions and dossier preparation for medical devices or pharmaceuticals.
- In-depth knowledge of ISO 13485, IEC 62304 and Class III medical…
View similar jobs with this employerSThreeEdinburgh- Potential to develop specialist expertise in medical device regulations.
- Ensuring product compliance with ISO 13485, IEC 62304 and relevant medical device…
Job Post Details
Senior Pharmacovigilance Officer - job post
Uxbridge UB11 1AF
£28,000 - £35,000 a year - Permanent, Full-time
Job details
Pay
- £28,000 - £35,000 a year
Job type
- Permanent
- Full-time
Location
Uxbridge UB11 1AF
Benefits
Pulled from the full job description
- Sick pay
- Life insurance
- Company pension
- Company events
- On-site parking
Full job description
- Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
- Assist in ensuring continuous oversight of all PV activities performed internally and by third parties.
- Support regulatory inspections, audits, and CAPA management.
- Contribute to PV governance activities and safety compliance monitoring.
- Provide oversight of Medical Information activities to ensure compliance with pharmacovigilance obligations.
- Ensure product complaints, adverse events, special situations, and safety information received through Medical Information are appropriately identified, processed, and reported.
- Support and perform reconciliation activities between Medical Information and other stakeholders
- Ensure deviation, CAPA, change control, and risk management processes.
- Drive inspection readiness activities across the PV system.
- Deliver pharmacovigilance training to internal stakeholders
- Coordinate the preparation, review, and submission of PSURs, RMPs and ACOs in accordance with regulatory requirements.
- Preparation and implementation and maintenance of approved RMM programmes.
- Coordinate the preparation, review, UK PSMF and all associated annexes.
- Ensure the PSMF accurately reflects the current pharmacovigilance system and organisational structure.
- Oversight and management of safety variations
Qualification:
- Essential Degree in Life Sciences, Pharmacy, Nursing, Medicine, or related healthcare discipline.
- Significant pharmacovigilance experience within the pharmaceutical industry.
- Strong knowledge of UK Pharmacovigilance legislation and MHRA GVP requirements.
Job Types: Permanent, Full-time
Pay: £28,000.00-£35,000.00 per year
Benefits:
- Company events
- Company pension
- Life insurance
- On-site parking
- Sick pay
Ability to commute/relocate:
- Uxbridge UB11 1AF: reliably commute or plan to relocate before starting work (required)
Education:
- Bachelor's (required)
Licence/Certification:
- UK Work Authorisation (required)
Work Location: In person
Let Employers Find YouUpload Your Resume