Johnson & Johnson seeks a Pharmacovigilance QA EMEA Auditor to lead routine audits and support regulatory inspections across multiple European locations.
This position operates within a global team dedicated to improving quality standards through pharmacovigilance auditing and collaboration with business partners. The role is based in Allschwil, CH, but opportunities exist in Italy, Belgium, France, Spain, and the UK, potentially under different requisition numbers.
Responsibilities
- Directs the planning, execution, and reporting of standard pharmacovigilance audits.
- Assists with non-routine audits covering data, facilities, and GxP processes.
- Joins assigned projects or cross-functional teams as directed by management.
- Provides support during regulatory inspections in various capacities.
- Helps create training materials when requested.
- Advises business partners on routine tasks, with occasional supervision.
- Collaborates with partners on compliance questions and consults on complex issues to maintain a unified departmental stance.
Requirements
- Bachelor’s degree or equivalent in natural or biological sciences.
- Excellent verbal and written communication abilities, including presentation skills.
- Strong analytical and teamwork capabilities.
- Proven ability to function effectively within a collaborative team environment.
- Fluent proficiency in English.
Nice to have
- At least two years of experience in a GVP-regulated setting, with specific exposure to pharmacovigilance activities.
About the company
Johnson & Johnson operates with the belief that health is paramount, striving to create a world where complex diseases are prevented, treated, and cured. The organization fosters an inclusive environment that values each individual, respecting employee diversity and dignity while recognizing merit.
- Commitment to preventing, treating, and curing complex diseases.
- Inclusive work environment that treats every person as an individual.
- Respect for employee diversity, dignity, and merit.
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