Position Overview
Johnson & Johnson IM is currently recruiting for a Pharmacovigilance QA Auditor Specialist. As a Pharmacovigilance QA EMEA Auditor Specialist, you will be part of a dynamic global team working to enhance quality across the Company through pharmacovigilance audit and business partner collaboration.
Key Responsibilities
Auditing
- Leads the planning, conduct and reporting of Pharmacovigilance routine audits
- Supports non-routine Pharmacovigilance audits of activities, data, internal facilities and processes in GxP areas
Project Management
- Participates in projects or serves on teams, as assigned by supervisor.
Inspection Support
- Supports regulatory inspections in various supporting roles.
Training & Development
- May assist in the preparation of training material if requested.
Subject Matter Expert / Point of Contact
- Provides consultation to business partners on routine tasks with occasional supervision.
- Cooperates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position.
Qualifications
Education
Bachelor’s or equivalent University degree required; Focused degree in natural/biological sciences or equivalent
Experience and Skills
Required
- A Minimum Bachelor’s or equivalent University degree required; Focused degree in natural/biological sciences or equivalent
- Strong verbal and written communication skills, including presentation skills
- Strong teamwork and analytical skills
- Ability to work effectively as part of a collaborative team
- Fluency in English
Preferred
- Minimum of 2 years’ experience in a GVP-regulated environment is preferred, with demonstrated exposure to Pharmacovigilance activities.
Other
- This position requires 10%-30% domestic and international travel
Johnson & Johnson is an Affi…
#J-18808-Ljbffr”, “datePosted”: “2026-05-18”, “hiringOrganization”: { “@type”: “Organization”, “name”: “Johnson & Johnson”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__435630287__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=438” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “High Wycombe” } } }Position Overview
Johnson & Johnson IM is currently recruiting for a Pharmacovigilance QA Auditor Specialist. As a Pharmacovigilance QA EMEA Auditor Specialist, you will be part of a dynamic global team working to enhance quality across the Company through pharmacovigilance audit and business partner collaboration.
Key Responsibilities
Auditing
- Leads the planning, conduct and reporting of Pharmacovigilance routine audits
- Supports non-routine Pharmacovigilance audits of activities, data, internal facilities and processes in GxP areas
Project Management
- Participates in projects or serves on teams, as assigned by supervisor.
Inspection Support
- Supports regulatory inspections in various supporting roles.
Training & Development
- May assist in the preparation of training material if requested.
Subject Matter Expert / Point of Contact
- Provides consultation to business partners on routine tasks with occasional supervision.
- Cooperates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position.
Qualifications
Education
Bachelor’s or equivalent University degree required; Focused degree in natural/biological sciences or equivalent
Experience and Skills
Required
- A Minimum Bachelor’s or equivalent University degree required; Focused degree in natural/biological sciences or equivalent
- Strong verbal and written communication skills, including presentation skills
- Strong teamwork and analytical skills
- Ability to work effectively as part of a collaborative team
- Fluency in English
Preferred
- Minimum of 2 years’ experience in a GVP-regulated environment is preferred, with demonstrated exposure to Pharmacovigilance activities.
Other
- This position requires 10%-30% domestic and international travel
Johnson & Johnson is an Affi…
#J-18808-Ljbffr…