Industrial Policies Manager
il y a 2 semaines
**Your Role in MedTech Europe**:
**MedTech Europe, **the European Trade Association representing the medical technologies industries is seeking a highly motivated professional who has a passion for healthcare and medical technologies.
You will be responsible (under strategic direction of the **Medical Devices Senior Manager, Merlin Rietschel) **for taking a lead role in contributing to the organisation’s goals in the **Medical Devices’ Regulation **area. This team’s work focuses on the implementation of EU Regulation 2017/745 (MDR) meaning this is a primarily member interfacing role with a strong regulatory focus.
**Your Key Responsibilities**:
**Key Projects**
- Provide direction and support the functioning of certain **industrial policies working groups,** e.g. post market surveillance and vigilance, device-drug combination products etc.
- Assist with analysing impacts of future legislations on the sector, and more long term the revision of the **MDR**:
- Develop and coordinate MedTech Europe responses to public consultations, position papers and presentations as identified by the working groups and **contribute to advocacy efforts**:
- Develop industry guidance for members on various topics related to the implementation of the **MDR**
**Members Management**
- **Lead working groups** to meet the objectives including coordination of the debate, building consensus and advise on possible successful political and legal strategies
- Liaise and coordinate with other **industry associations and stakeholders in Brussels**
**Representation**
- **Represent the association** at external meetings involving EU institutions, stakeholders and policy makers.
**Your profile**
- Has a genuine **passion for healthcare and use of (medical technology) innovation** in healthcare legislation
- Holds a university degree or other relevant qualifications in **Biomedical Engineering (or other relevant scientific discipline), European Studies, Law, Political Science**:
- Has **minimum 5 years’ experience **of working in medical technology industry (technical or regulatory position), for instance from having worked for a Notified Body, a medical device manufacturer, or EU institution
- Has a strong understanding of **EU policies and the functioning of the EU (a must)**:
- Is fluent in both written and spoken **English,** other EU languages are an advantage
- Has the ability to **communicate effectively with multicultural stakeholders**:
- Is **well-organised **with sound project management skills and always strives for **operational excellence**:
- **Analytical** skills: has the proven ability to analyse, summarise and communicate on complex legal and technical issues.
- Is a **team player **who can work **proactively** and **independently** within complex teams and is open to learn and receive **constructive criticism**:
- Has excellent command of **MS Word, Excel, PowerPoint & Outlook**
**Offer**
- Competitive Salary + Performance Bonus, Lunch Vouchers, Pension Plan, Medical Plan (+ Family), Mobile Phone Subscription, Laptop and Transport Reimbursement
- Be a representative of a well-established and innovative European industry
- Opportunity to be a member of a motivated, dynamic and international team (regular team events)
- Opportunity for trainings and personal development
**INTERESTED?**
For more information: Call **EMMA WAITES **at the number**:02 738 02 63 GSM 0475 614967**
- MedTech Europe is an equal opportunity employer._
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