drjobs Head of Regulatory for a core product incl. Project Management

Head of Regulatory for a core product incl. Project Management

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Cologne - Germany

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

At Vivalyx a medical technology startup based in Aachen were on a mission to save the lives of those suffering from organ failure. Our innovative approach aims to significantly improve the vitality and availability of donor organs. As we gear up for certification and related studies were seeking dedicated team members (m/f/d) to join us starting as soon as possible for 32-40 hours per week.

Tasks

As the Head of Regulatory Affairs and Product Management you will lead the registration and market launch of a dedicated product. You will be the go-to person for regulatory matters of one of our core products both within our team and to external partners. Your responsibilities will include crafting and implementing strategies to meet regulatory requirements from strategic planning to preparing technical documentation in collaboration with our internal team and external partners. Given our small team size you will also be hands-on in writing regulatory documents. Additionally you will manage negotiations with partners and suppliers ensuring that our operations comply with quality management standards such as ISO 13485 and 21 CFR 820.

Requirements

Requirements

  • Passion for working in medical technology development
  • Strong sense of ownership drive independence and commitment
  • A technical or scientific degree or equivalent training
  • Several years of experience in a regulatory position in the medical device sector with broad responsibilities across the regulatory spectrum (i.e. companies with five or less people in regulatory such as startups or SMEs)
  • Expertise in regulatory affairs and project management including liaising with regulatory bodies
  • Experience with ISO 13485 ISOCFR 820 and MDR
  • Preferably knowledge of standards such as IEC 60601 and IEC 62366
  • Proficiency in Microsoft Office and fluent in English both written and spoken
  • Residence within a maximum commute time of 1.5 hours to Cologne and availability to work from the office at least once a week for team collaboration

Benefits

We provide the opportunity to work on groundbreaking technology that has a meaningful impact. Youll be part of a dynamic highly skilled and motivated team. We prioritize flexibility offering mobile working conditions and a flat hierarchical structure. In addition we support professional development and career growth along with an attractive employee participation program.

We look forward to hearing from you by July 18.

Employment Type

Full Time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.