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

Medical Information Officer Pharmaceutical jobs

Sort by: -
    • Ensure product complaints, adverse events, special situations, and safety information received through Medical Information are appropriately identified,…
    • This key role will provide administrative and coordination support for CQC compliance, incident reporting (Datix), policy management, and information governance…
    • View all PrimaryCareCareers jobs - Stowmarket jobs - Governance Officer jobs in Stowmarket
    • Salary Search: Governance & Compliance Officer salaries in Stowmarket
    • See popular questions & answers about PrimaryCareCareers
  • View similar jobs with this employer
    • Monitor regulatory/pharmaceutical regulations for the relevant therapeutic areas and share information internally.
    • Preparation and submission of variations.
    • To ensure Business compliance with MHRA’s Good Distribution Practice guidelines (2013/C 343/01) and corresponding legislation relating to the wholesale of…
    • Ensure tracking and update of relevant regulatory information in Novartis compliance systems and trackers as provided by RA sub-team representatives.
    • Bachelor’s degree in life sciences, healthcare, pharmacy, or information management.
    • Manage submission-readiness of clinical documents, ensuring compliance with…
    • Industry Tenure: 10+ years of pharmaceutical industry experience specifically within Quality Assurance.
    • You are the independent quality authority ensuring that…
    • The Director, Regulatory Platforms holds strategic oversight and operational accountability for the technology systems that power CSL's Global Regulatory…
  • View similar jobs with this employer
    • You'll set global labelling strategy, balancing business need against the core obligation of getting benefit/risk information right for the people relying on it…
    • Extensive clinical experience and proficiency in pharmaceutical care.
    • The Head of Clinical Operations is accountable to the Clinical Director for the management…
    • This check will provide information about employees who have been dismissed for fraud or dishonesty offences.
    • To have understanding, and possibly experience, of…
    • Assure that status of information is timely and accurate.
    • Teledyne Digital Imaging are looking for a Senior Export Analyst to manage the operational side of the…
    • Experience within a medical device or healthcare manufacturing industry in a regulatory or quality role.
    • You will be responsible for a portfolio of cutting-edge…
    • Ability to analyse complex information, influence stakeholders, and drive change across matrix organisations.
    • This role is based in London, United Kingdom.
    • Experience in the pharmaceutical industry with relevant diagnostics or in vitro diagnostics focus.
    • Design and deliver global regulatory strategies for precision…

People also searched:

information manager
information officer
information specialist
librarian
medical assistant
medical devices
medical receptionist
medical sales
medical secretary
medical writer

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