drjobs Head of Product Omnisol incl Regulatory mfd

Head of Product Omnisol incl Regulatory mfd

Employer Active

1 Vacancy
The job posting is outdated and position may be filled
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

Aachen - Germany

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

We Vivalyx are a medical technology startup from Aachen dedicated to saving people suffering from organ failure. Our goal is to significantly increase the vitality and number of donor organs. The company is currently in the preparation phase for certification and the associated studies. For this purpose we are looking for new colleagues (m/f/d) starting from 01.06.2024 (or later) for 3240 hours a week.

Tasks

As the Head of Product incl. Regulatory your role encompasses driving the development registration and market entry of our core product while also acting as the primary contact for regulatory issues among both our team and external partners. You will be tasked with formulating and executing strategies to adhere to regulatory requirements overseeing everything from strategic planning to the preparation of technical documentation in collaboration with our internal and external teams. Since we are a small team you will be also required to write regulatory documents yourself for the initial period. Additionally you will negotiate agreements with partners and suppliers ensuring our operations align with quality management standards set forth by ISO 13485 and 21 CFR 820.

Requirements

Motivation and enjoyment of work especially in medical technology and development

Strong ownership drive independence and commitment

Proven leadership capabilities

Technical or scientific degree or comparable training

Several years of professional experience in the medical device sector preferably in product management RA and project management including contact with regulatory bodies

Preferably experienced in applying ISO 13485 ISOCFR 820 and MDR

Confident handling of Microsoft Office and proficient English in spoken and written form

Benefits

We offer the opportunity to work on highly innovative cuttingedge technology with a good purpose in a dynamic highly qualified and highly motivated team. In addition we work very flexibly mobile and in flat hierarchies. We also offer further training and career advancement opportunities as well as an attractive employee participation program.

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.