Skip to main content
Post your CV and find your next job on Indeed!

Medical Biotechnology jobs

Sort by: -
    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
  • View similar jobs with this employer
    • The Veterinary Medicines Directorate (VMD) is an Executive Agency of the Department for Environment, Food and Rural Affairs (Defra) and is responsible for…
    • You will also have the opportunity to oversee contract research organisations (CROs) that conduct in vivo studies of our immunotherapy candidates.
    • Contract type: PAYE (Inside IR35).
    • Design and execute innovative in vitro investigative toxicology experiments or technical work programs to support Project…
    • Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety…
  • View similar jobs with this employer
    • Governance & Compliance: Establish and oversee global governance frameworks, ensuring all medical activities uphold the highest ethical and scientific standards…
    • Bath ASU which produces thousands of aseptically (sterile) compounded injectable pharmaceutical products each day for hospitals and patients who are fighting…
    • Ensure compliance with applicable medical device regulations and internal quality standards.
    • The Precision Medicine Director is responsible for developing and…
    • Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review.
    • As Director, Clinical Quality Assurance Compliance you will lead quality assurance activities across clinical development programs in global teams.
  • View similar jobs with this employer
    • Provide operational and leadership continuity across Immunocore's medicinal product lifecycle by deputizing for the Director, Quality Assurance, and supporting…
    • Involvement in bringing regulated medical devices to patients.
    • Experience with medical device quality management systems (QMS).
    • The GIST Access Acceleration Lead will leverage clinical understanding, expertise of Evidence Based Medicine, alongside deep global payer knowledge and…
    • Experience within a regulated environment, ideally diagnostics, medical devices, biotechnology or life sciences.
    • Strong analytical and problem-solving skills.
    • Clinical PM roles in healthcare delivery could involve coordinating regulated programmes that balance clinical outcomes, operational efficiency and stakeholder…

People also searched:

medical writer
microbiology
molecular biology
synthetic biology
biotechnology graduate
biotechnology internship
life science
medical assistant
medical devices
medical receptionist

Job Post Details

Senior Pharmacovigilance Officer - job post

Milpharm Ltd
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