Job DescriptionSUMMARY OF POSITION:The role will use technical expertise to:Support the setting of Pharmacovigilance and Product Quality Complaint cases in the UKSupport the Pharmacovigilance Manager in maintaining, developing and implementing Pharmacovigilance compliance procedures.Priority is given to Pharmacovigilance case setting which must be completed to a high standard within short deadlines. This involves working with the technical and veterinary teams who gather the case information, to ensure that information gained is sufficient and to a high clinical standard to allow each Pharmacovigilance case to be fully assessed and coded within PV Works.The role will also assist the current team of Pharmacovigilance Officers by giving technical support.The role will assist the Pharmacovigilance Manager with the maintenance, development and implementation of Pharmacovigilance compliance procedures in line with internal and external guidance.The successful candidate will be a vet, member of the RCVS ( Royal College of Veterinary Surgeons)MAJOR ACTIVITIES AND RESPONSIBILITIES:To enter data for pharmacovigilance cases in the appropriate system within the deadlines.To assess cases for VEDRA coding and final causality, with explanation of findings.Apply technical knowledge to improve pharmacovigilance case technical content, case quality and consistencyTo liaise with Competent Authorities as requiredTo liaise with Vet advisers and the Technical Product Support Group to ensure accurate case data is available and to reconcile anomaliesTo work with Global colleagues to understand the Pharmacovigilance requirements for different products.Product Quality Complaints setting in PV WorksTo assist the Pharmacovigilance Manager with maintaining, developing and implementing Pharmacovigilance compliance procedures.To provide backup to the Pharmacovigilance manager and PQC DPOC to ensure compliance with procedure and deadlines as required.To give advice/training to Commercial, Pharmacovigilance and Technical product Support Group as required.Major challenges of the role are:To source accurate data from practices and use technical knowledge to assess this when case setting.To liaise with global colleagues to discuss pharmacovigilance cases.To assess operational protocols and implement improvements.To ensure all cases are reported in the required timescaleTo prioritize work loadsAdditional location(s) Compensation Information:Required Skills: Adverse Event Report, Compliance Monitoring, Data Analysis, Decision Making, Drug Safety Surveillance, Pharmaceutical Regulatory Compliance, Pharmacovigilance, Regulatory Compliance, Regulatory Reporting, Risk Management, Veterinary Products, Veterinary ServicesPreferred Skills: Current Employees apply HERECurrent Contingent Workers apply HERESearch Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: RegularRelocation:No relocationVISA Sponsorship:NoTravel Requirements:No Travel RequiredFlexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):N/AJob Posting End Date:10/28/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. SummaryLocation: GBR - Buckinghamshire - Milton KeynesType: Full time
Pharmacovigilance Veterinary Officer in Milton Keynes employer: Merck Sharp & Dohme (MSD)
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