ARNOWA GmbH | Germany | 33xxx Salzkotten | Permanent position | Part time - flexible / Full time / Home office | Published since: 18.01.2026 on stepstone.de
Quality and Regulatory Management Staff (m/f/d)
You have an organizational talent and a strong eye for detail? And do you want to introduce your strengths in quality management in a dynamic, innovative environment? Then you're right with us! We are a leading trading company for medical devices and pioneers in digital trading. For over ten years we have been in business and our growth is based on innovative strength, digital strength and a clear focus on quality. Our goal is to offer our customers the best possible products and deliver them the highest quality and service. We therefore look for you – from now on and with at least 20 hours a week – for our team at the Salzkotten site! As a member of our QM team, you take responsibility for compliance with regulatory requirements and the continuous development of our quality management system. Whether ISO 13485, ISO 14001, MDR or REACH – you make sure our products and processes meet the highest standards! !
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Your tasks • Your profile • What we offer
You ensure compliance with all relevant quality standards and regulations. You keep the developments in the relevant legislation in mind and ensure that all legislative changes are implemented efficiently in our product portfolio. You support ensuring compliance with all relevant policies, laws, standards and country-specific requirements. You are researching, analysing and independently assessing legal requirements, standards and regulations at national and EU level – e.g. MDR, REACH, CLP, Biocide Regulation or PSA Regulation. You support the clarification and answering questions concerning product compliance, labelling requirements and risk assessments. You will deal with topics such as environment, health, workplace safety, sustainable development and EHS compliance. You carry out internal audits. You identify quality problems and develop solutions. You raise, analyze and prepare quality indicators – with the aim of achieving continuous improvements and supporting management assessment. You train colleagues on quality standards and procedures. You analyze process risks and take appropriate measures to optimize them. You create technical documentation for new products and update the existing files. You work closely with suppliers and customers to meet quality requirements. You support the certification of the company according to standards such as ISO 13485, ISO 9001 or ISO 14001.
Studying in the technical, scientific or environmental field – as an alternative an education with a focus on quality management or a comparable qualification First professional experience (1–2 years) in quality management or regulatory affairs – ideally in the medical device, PPE or food industry. Experience with regulatory requirements for medical devices, PSA or biocidal products Experience in the field of EHS and environmental management is a plus, but no requirement Knowledge of relevant quality standards and systems (e.g. ISO 13485, ISO 14001, Regulation 2017/745, Regulation 2016/425, Regulation 10/2011) Good knowledge of English Safe handling of legal texts, standards and regulations Fun in innovation and analytical thinking Proactive attitude and a structured, independent and responsible way of working
An unlimited setting in a fast-growing and modern working environment An attractive salary including individual performance assessment and success-oriented bonus A monthly voucher card or an Urban Sports membership as a tax-free property cover Christmas money as appreciation for your use Flexible working in the sliding time model with up to two home office days per week A motivating working environment with modern equipment in our new company A dynamic corporate culture with design space and development perspectives Room for personal and professional development in a dedicated team
Location
![]() | ARNOWA GmbH | |
| 33154 Salzkotten | ||
| Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
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