Regulatory & Technical Consultant Active-Medical Devices
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs, or auditing in the area of medical devices. We are a worldwide operating and fast-growing consulting organization in the medical device sector with our largest base in Europe, the Netherlands, and local teams in China and the USA.
This is what you will be doing at Qserve:
As a Regulatory & Technical Consultant of our company, you provide specialist consulting services to obtain, maintain, or expand market access for our customers to various Medical Device markets (EU, USA, China). This could involve supporting customers transition from the MDD to the MDR or gain CE marking or FDA clearance.
As a consultant, no two days or customers are the same. You may be required to build a technical file to support CE marking or 510(k) submission or similar approvals for active medical devices and medical software. It could also include strategy planning, in-depth reviews of performance evaluation or risk management data, creating and reviewing quality management systems, performing gap analyses, or perhaps delivering customer training.
You will be part of a team, no one is an expert on everything, so we support each other to play to our strengths so that we provide the best service to customers. This position offers a great opportunity to apply your expertise inactive devices and medical software and continue to build your expertise in artificial intelligence. For this specific expert area, you will be the point of contact for colleagues and customers. You will pro-actively follow the new developments and trends in the market to share within our Knowledge Center (blogs, whitepapers, news items, presentations or similar to promote knowledge base and brand of Qserve).
Is this your DNA?
Are you passionate to help customers? Are you able to find the right balance between business needs and quality of work in the interest of the customer, while always staying close to ethical and professional values and pride in the work that you deliver? Do you have a practical approach and being creative in finding pragmatic solutions within your projects for customers? Then please take a look at our career opportunities at Qserve. We would like to get in contact with you!
Why choose Qserve?
Qserve has an international and dynamic work environment in which you can learn, develop, and operate in the innovative, fast-moving medical device sector. We offer flexibility and diversity in terms of clients, devices, technology, roles (author, reviewer, expert, trainer, auditor, etc.), and projects. Work together, learn from and be part of a strong international team with technical, regulatory, quality, and clinical competences (altogether over 500 years’ experience). And, last but not least we offer a balanced set of core benefits that we believe are important to all employees.
“Global reach, practical approach, experienced team”
Getting excited about a career as a consultant in the dynamic and innovating world of medical devices? Then please submit your resume and letter of motivation to firstname.lastname@example.org or use our application form on our website: http://www.qservegroup.com/about-us/application-form.
For more information about our company, you can always visit our website (www.qservegroup.com) or contact our HR department at +31 20 78 82 630.