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ContactWorking timeFull-time LocationHerdecke Start dateas soon as possible Contractby agreement
EN
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Your tasks with us.
- • Maintain and continuously improve the international pharmacovigilance system.
- • Process reports of adverse effects and product risks from spontaneous reports, clinical studies and scientific literature.
- • Document and follow up adverse-event reports, including entries in the global safety database.
- • Prepare and maintain pharmacovigilance documents for regulatory dossiers, including RMP, PSUR and PSMF.
- • Prepare and revise reference documents such as summaries of product characteristics and package leaflets.
- • Provide medical and scientific support for the product portfolio to healthcare professionals, users and field staff.
- • Create and maintain standard operating procedures for relevant workflows.
What you bring with you.
- • Completed degree in biology, pharmacy, medicine or a comparable natural-science discipline.
- • Experience in drug safety is an advantage; qualified career starters can enter through a structured trainee programme.
- • Very good written and spoken German and English.
- • Confident use of databases and Microsoft Office applications.
What we offer you.
- Family-owned company: A secure, permanent position with long-term prospects, respectful collaboration and short decision paths.
- Health & benefits: Attractive compensation, 30 days of annual leave, employer-supported pension benefits and JobRad bicycle leasing.
- Development & training: Structured onboarding and financial support for external specialist training courses and seminars.
Apply in just a few minutes.
Open our online application portal and submit your documents in a few clear steps.