Regulatory Affairs Specialist II - Maastricht, Netherlands
1 dag geleden

Functieomschrijving
Why Merit?
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
SUMMARY OF DUTIES
DUTIES & RESPONSIBILITIES
- Assist with determining global regulatory pathways for various projects including product classification and type of regulatory submission or rationale required.
- Participates on various teams to define regulatory requirements of international submissions or regulatory rationales.
- Identifies guidance documents, international standards, Consensus Standards and assists teams with their interpretation.
- Prepares regulatory submissions to the Ministries of Health wherever required.
- Interacts with various levels of management, external agencies and companies.
- Assist with developing, maintaining and analysing department systems and provides training when needed.
- Participates in and assists with the preparation of Notified Body Audits and other governmental inspections as directed.
- Performs other related duties and tasks, as required.
SUMMARY OF MINIMUM QUALIFICATIONS
- Education and/or experience equivalent to a Bachelor's Degree in the biological, physical, engineering or health science disciplines and four years of related experience.
- Strong knowledge of regulations, the Medical Devices Directive (93/42/EEC, as amended), Medical Device regulation (2017/745), MEA region and ISO 13485 Quality System Standards.
- Supervisory skills are preferred.
- Self-motivated, self-directing, strong attention to detail and excellent time management skills.
- Strong interpersonal skills and the ability to communicate well – verbally and in writing – with others.
- Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.
We are Global
Founded in 1987, Merit Medical Systems, Inc. is a leading manufacturer and marketer of proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care and endoscopy. Merit serves client hospitals worldwide with an international sales force and clinical support team totalling in excess of 500 individuals. Merit employs approximately 6,300 people worldwide.
Merit Medical EMEA currently has over 300 employees, spread over more than 20 countries in the EMEA region.
Merit Maastricht (The Netherlands) is the European Headquarters and Distribution Center of Excellence. Much of Merit Medical's world-class customer service happens here along with our excellent physician training courses. More than 100 employees work at this growing Merit campus and enjoy many benefits, such as flexible working hours and competitive salaries as well as learning opportunities and internships.
Culture
A supportive and collaborative environment make Merit Medical a friendly, enjoyable place to work. We are proud of our energetic and dynamic culture. Diversity & Inclusion is evident here with a 50/50 ratio of male and female employees and more than 30 nationalities. We value every employee as an individual.
To see more on our culture, go to
Soortgelijke banen
At Merit Medical, our mission is to create innovative medical devices that improve lives. · ...
2 weken geleden
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. · We are Global · Founded in 1987, Merit Medical Systems, Inc. is a ...
2 weken geleden
A career of exploration and innovation in regulatory affairs at Medtronic. · ...
5 dagen geleden
You will focus on supporting regulatory affairs field actions and addressing inquiries from the Competent Authority, customers, tenders, marketing, and sales teams. You will also provide guidance and advice to the sales team to ensure compliance with EU and local legislation in t ...
1 maand geleden
This is a Medical Affairs Specialist role with Boston Scientific in EMEA. The key responsibilities include building relationships with Key Opinion Leaders and engaging them on areas of strategic importance to BSC. · Evaluate external clinical research proposals and collaborate wi ...
1 maand geleden
We are seeking a Medical Affairs Specialist for our EMEA region to build relationships with Key Opinion Leaders · - Evaluate external clinical research proposals · - Participate in developing clinical evidence plans that align with our strategic focus · - Communicate scientific ...
1 maand geleden
We're looking for a Medical Affairs Specialist EMEA to build relationships with Key Opinion Leaders, engage them on their fields of interest, on areas of strategic importance to BSC and on research. · Evaluate external clinical research proposals. · Capture European Research Need ...
1 maand geleden
We're looking for a Medical Affairs Specialist EMEA who will build develop and maintain relationships with Key Opinion Leaders engage them on their fields of interest on areas of strategic importance to BSC.<br><p>Key Responsibilities</p><ul><li>Evaluate external clinical researc ...
1 maand geleden
We're looking for a Junior Quality Assurance Specialist to support quality systems and compliance activities within a regulated Life Sciences environment. · This is a great opportunity for someone early in their QA career to gain broad exposure across multiple quality areas. · Su ...
2 weken geleden
We're looking for a Junior Quality Assurance Specialist to support quality systems and compliance activities within a regulated Life Sciences environment. · This is a great opportunity for someone early in their QA career to gain broad exposure across multiple quality areas. · ...
2 weken geleden
The Quality Assurance Specialist supports quality systems programs and processes ensuring compliance with internal policies regulatory standards and external guidelines providing analytical oversight supporting audit readiness contributing to continuous improvement of global qual ...
3 weken geleden
The Quality Assurance Specialist is responsible for supporting maintaining and enhancing quality systems programs and processes to ensure compliance with internal policies regulatory standards and external guidelines. · This role provides analytical and compliance oversight suppo ...
3 weken geleden
We are looking for a Quality Control Officer to support the team of the Quality Improvement Team by reviewing raw data and laboratory documentation to confirm adherence to validated methods and SOPs. · ...
1 maand geleden
We are looking for a Quality Control Officer to support the team of the Quality Improvement Team by reviewing raw data, reports, · and laboratory documentation to confirm adherence to validated methods, · SOPs, regulatory requirements, · and best practices, · driving quality impr ...
1 maand geleden