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    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
    • The successful candidate will play a pivotal role in our laboratory dedicated to ensuring the efficacy and safety of anti-seizure medications through precise…
    • Create medical information standard letters.
    • Final medical sign off for copy approval.
    • Provide medical information standard letters to external customers.
    • Ensure compliance with laboratory quality standards, health and safety requirements, and good laboratory practices.
    • TEMP - ONSITE - 22.77/hr PAYE 35hr wk.
    • Experience in working in a scientific laboratory and health and safety requirements.
    • Maintenance roles, particularly those required to work in laboratory…
    • Successful candidates will be expected to have a medical.
    • Ensuring the laboratories are clean, tidy and free from clutter.
    • Pro rata for job share.
    • Experience of scientific support work in a process laboratory type of environment, particularly dosimetry.
    • Experience of scientific support work in a process…
    • When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.
    • Significant, current experience working in a molecular diagnostic laboratory.
    • Performing audits, investigating incidents, contributing to laboratory…
    • The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio and will also have…
    • A varied and influential role within a respected UK analytical laboratory.
    • At least ten years’ relevant experience in an analytical laboratory environment.
    • Experience supporting laboratory improvement projects.
    • Support development of junior scientific staff.
    • Monitor laboratory quality indicators and performance…
    • Experience working within a Haematology laboratory.
    • This role requires prior experience in a UK-based laboratory relevant to the post.
    • Experience in teaching and training both medical and non-medical staff stakeholders.
    • Lead and contribute general clinical support, for example by providing…
    • A presentation may also be included in the interview that will assess your scientific and project management skills.
    • National: £42,665 - £46,765.

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Job Post Details

Senior Pharmacovigilance Officer - job post

Milpharm Ltd
Uxbridge UB11 1AF
£28,000 - £35,000 a year - Permanent, Full-time
Responded to 51-74% of applications in the past 30 days, typically within 3 days.

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

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