Pre Market Quality and Regulatory Specialist (m / f / d)

Dedalus HealthCare; Bonn; Hybrid; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

A leading healthcare company in Bonn is seeking a Pre-Market Quality and Regulatory Specialist. You will ensure process adherence for pre-market procedures and regulatory compliance for development projects. This role offers a permanent contract with flexible working hours and a focus on professional growth.

Leistungen

Permanent employment contract

Flexible working hours

Home office options

Up-to-date company cell phone

Company pension plan

Group accident insurance

Qualifikationen

• Minimum 3 years of experience in a regulated industry.
• Working independently towards project deadlines.
• Expertise in ISO 13485, MDR, and IVDR.

Aufgaben

• Ensuring process adherence for pre-market procedures.
• Creation and maintenance of key regulatory deliverables.
• Performing internal audits and defending activities during inspections.

Kenntnisse

Regulatory Affairs

Attention to Detail

Project Management

Ausbildung

University Degree (Engineering, Computer Science or Science)

Tools

Microsoft Office

Jobbeschreibung

And do you want to make healthcare safer better and more reliable

Join our Team!

We are looking for you located in Bonn (Hybrid) as a

Pre-Market Quality and Regulatory Specialist (m / f / d)

Ensuring process adherence for the pre-market procedures

Completeness of design history files and regulatory submissions

Regulatory and process conformance for development and maintenance projects as a member of cross-functional teams

Creation and maintenance of key regulatory deliverables of the projects

Regulatory and CE submissions in cooperation with regional QARA organizations

Ensuring the adherence to the medical device risk analysis process as risk moderator of the

development team

Facilitate regulatory compliance in design control processes to ensure that there are no compliance issues during regulatory inspections

Performing internal audits and defending Dedalus pre-market activities during external regulatory inspections and audits

You bring along :

University Degree (Engineering Computer science or Science) or equivalent

Minimum 3 years of experience in a regulated industry preferably medical device pharmaceutical or related holding a position in project management quality management or quality assurance and regulatory affairs position.

Working independently towards project deadlines and strong attention to detail with the ability to analyse understand and interpret regulations and standards for a more general business audience

Subject matter expert in regulatory affairs with in-depth knowledge of relevant health care quality standards and requirements including ISO 13485 ISO 14971 IEC 62304 IEC 62366 Medical Device Directive and new Medical Device Regulation MDR and IVDR

Awareness of Medical Device product safety and Security Standards including ISO 27001 GDPR and other regulation as determined by product availability (including ANVISA CMDCAS FDA SFDA)

Expert PC operation skills including knowledge of enterprise-wide software applications Microsoft Office applications required (Intermediate to Advanced preferred)

Mandatory Language Skills : German English (upper intermediate or better)

What we offer :

Permanent employment contract with attractive salary for a long-term perspective

Flexible working hours and working time models for a good work-life-balance

Home office incl. TicketPlusCity card from Edenred

Flexitime model

Innovative workplace with the opportunity to shape the work environment independently and to continuously develop your skills

Targeted advancement through training and specialist further education

Up-to-date company cell phone with dual-sim (Android or iOS) also for private use

Free parking spaces

Free drinks and weekly fruit basket

Company pension plan and working time accounts

Group accident insurance (also valid for accidents during free time)

Foreign health insurance for business trips

Regular activities and social events in the team at the site and in the organization

Be part of our innovative power and shape the future with us!

teamdedalus #together4success #dedalusgroup

We are looking forward to receiving your online application!

Severely disabled applicants will be given special consideration if they are equally qualified.

Dedalus HealthCare GmbH

Human Resources

54294 Trier

We are Dedalus come join us

Dedalus is committed to providing an engaging rewarding work experience that reflects the passion our employees bring to our mission of helping clinicians and nurses deliver better care to their served communities.

Our company fosters a culture where employees are encouraged to learn and innovate and to enable and enhance clinical co-operation and processes while making a meaningful difference for millions of people around the world. Each person is the end point and the starting point of the Groups activities and the ultimate beneficiary. For this reason we are so proud of doing our very special jobs each day.

Our company is enriched by a diverse population of 7600 people in more than 40 countries that work together to innovate and drive better healthcare options for millions of patients around the world. We are the people of Dedalus.

Our Diversity & Inclusion Commitment sets out Dedalus approach to ensuring respect inclusion and success for all our colleagues and the wider communities we operate in. It is imperative for us to share our commitment and dedication to ensure an inclusive and diverse workplace. We recognise that we have improvements to make and on this journey we must remain authentic and realistic but also ambitious.

Our diversity & inclusion commitment Dedalus Global

Life Flows Through Our Software

Required Experience :

Unclear Seniority

Key Skills

Employment Type : Full-Time

Experience : years

Vacancy : 1

Regulatory Specialist • Bonn, North Rhine-Westphalia, Germany