Working Student – Regulatory Monitoring

Job not on LinkedIn

🔥 17 hours ago

🇩🇪 Germany – Remote

⏱ Part Time

⚪️ Entry-level

🚔 Compliance

🚫👨‍🎓 No degree required

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Johner Institut GmbH

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2005

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Johner Institut GmbH is a German regulatory and training services firm specializing in medical devices and in vitro diagnostics (IVD). The company helps manufacturers with regulatory affairs, market access (EU/UK/CH/US), quality and information security management systems, technical documentation, clinical and performance studies, product testing (biocompatibility, electrical/EMC, IT security) and penetration testing, and provides authorized-representative/legal-manufacturer and outsourcing services. It also offers education (seminars, e-learning, Auditgarant templates), RegTech/SaaS tools for regulatory intelligence and post-market surveillance, and consulting to implement AI/AI Act compliance and digitalization for medtech clients.

📋 Description

• Research and assessment of relevant regulations • Preparation of reports for the Regulatory Intelligence solutions Regulatory Radar and Post-Market Radar • Supporting the service team with customer inquiries • General database maintenance • Independently reviewing automated regulatory monitoring for assigned markets and regulatory groups • Contributing to the optimization of internal processes in Regulatory Monitoring

🎯 Requirements

• Currently enrolled as a student for at least one year • Ideally pursuing a degree in medical engineering, regulatory affairs, natural sciences, engineering, or a comparable field of study • Interest in regulations relating to the medical device and/or pharmaceutical industries • Independent, meticulous, and structured approach to work • Ability to quickly become familiar with new topics and digital tools • Basic knowledge of HTML structures and their use for automated data collection from websites is an advantage, but not required • Excellent written and spoken German and English skills • Current proof of enrollment and transcript of records required with the application

🏖️ Benefits

• Support for and promotion of professional and personal development • Flexible working arrangements with no core working hours • Option to work fully remotely • Option to work remotely or from our Konstanz or Frankfurt office • Two team events per year • Workation opportunities • Innovative working environment offering plenty of scope for shaping processes and implementing change • Great team atmosphere and strong sense of collaboration