20 beste vacatures voor de functie van program manager in amersfoort, ut (nieuwe medewerkers gezocht)

Regulatory Affairs Specialist, Post Market (32 - 40hrs per week)
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GlaxoSmithKline —Amersfoort
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- Microsoft Excel
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Digital Product Manager App
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Elekta —Veenendaal
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Director of Business Development
Xebia Group —Hilversum
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JDE Peet's —Utrecht
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Res2 B.V. —Utrecht Leidsche Rijn
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SCD Santander Consumer Finance (Netherlands) —Utrecht
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Business Development Manager - Export Europe (all genders)
FrieslandCampina —Amersfoort
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- Master
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- Flexibele werkuren
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Portfolio Manager
Kramp GmbH —Utrecht
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Requirements Engineer (Medewerker Requirements)
Ministerie van Defensie —Amersfoort
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Digital Program Manager – Commercial Growth
ViCentra B.V. —Utrecht
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Regulatory Affairs Specialist, Post Market (32 - 40hrs per week)

Applied Medical Europe B.V. -
Amersfoort

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Vacaturegegevens

Secundaire arbeidsvoorwaarden

Pensioen
Bedrijfsfeesten

Kwalificaties

Engineering
Engels
Bachelor
Communicatieve vaardigheden

Volledige vacaturetekst

Overview:

Job Description:

Are you enthusiastic about building your career in regulatory affairs and eager to deepen your expertise in post market product support?

We are looking for a driven Regulatory Affairs Specialist to join our Post Market Regulatory Team at Applied Medical’s European headquarters in Amersfoort (NL).

In this role, you will be a key member of a small and highly collaborative sub team focused on complaint handling and post market regulatory activities.
You will be responsible for coordinating all regulatory efforts related to customer complaints processing, ensuring timely and accurate reporting to European authorities.
The position plays a coordinating role, ensuring smooth collaboration between field teams, internal departments, and external parties.
You will work closely with Customer Service, Quality, Sales, our U.S. Regulatory team, and external customers to ensure complaint data is handled, processed, and communicated with the highest level of quality and accuracy.

The Post Market team consists of seven members, with the immediate sub-team including four specialists.

Key Responsibilities

Review and verify complaint data to ensure accurate and complete regulatory reporting
Submit mandatory reportable events to European authorities within strict timelines and track all follow up activities
Review and prepare final responses and closing reports
Ensure compliance with European regulations and internal quality and reporting standards
Collaborate closely with QA Engineers responsible for technical complaint investigations
Support additional regulatory activities such as recall notifications, and internal/external regulatory requests

Requirements:

Bachelor’s degree (HBO) in Engineering, Medical Affairs, Regulatory Affairs or related field
1+ years relevant working experience
Excellent oral and written communication skills in English
Knowledge of another European language is a plus
Experience in Medical Devices, knowledge of Quality Management System, ISO or CE marking is a plus

We Offer:

An international working environment, fueled by respect and a healthy work-life balance tailored to the business and team member’s needs
27 paid vacation days (based on fulltime contract) with option to purchase five additional days
This is mainly an on-site role with hybrid options
Commuting allowance of €0,23/km or full coverage of public transportation costs
A wide variety of internal trainings and development possibilities and a tuition program for external trainings
The opportunity to pro-actively work on your vitality and fitness
State-of-the-art facilities, including green areas, in-house restaurant and gym
Additional benefits, such as:
- Attractive pension scheme (your contribution at 4%, ours at 12%)
- €50 net monthly health insurance contribution
- Two (paid) days per year dedicated to volunteering activities
- Several fun company events and meaningful initiatives organized throughout the year

At Applied Medical, we are committed to make a meaningful, positive difference, each and every day. Within our European headquarters in Amersfoort (NL), we develop, manufacture and support the implementation of our advanced medical devices across Europe and the MENA region. Applied’s team members enjoy working in an environmentally friendly and international environment, in which people of diverse backgrounds are valued, challenged, and acknowledged. We support our team members by giving them opportunities of ongoing learning and education, possibilities to take part in community volunteering activities and a variety of onsite exercise classes and health activities.

If you are passionate about working in an organization that allows you to make decisions based upon what is right for the patient, customer, community and environment, Applied Medical is the place for you.

Interested?

Would you like to be part of our expanding team? If the answer is yes, we'd love to get to know you and look forward to hearing from you!

For more information regarding our hiring process, click here. If you have any questions, feel free to contact us via [email protected] or +31 (0)33 7548713.

Not the right job for you? Take a look at our other vacancies and follow us on LinkedIn.

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Verfijn je zoekopdracht

program manager vacatures in amersfoort, ut

Regulatory Affairs Specialist, Post Market (32 - 40hrs per week)

Junior Project Leader

Project Manager Category Management

Project Manager

Head of Sustainable Solutions

Senior Program Manager Change

Business Analyst

Digital Product Manager App

Senior Project Manager / RTE

Omgevingsmanager

Digital Product Manager (Easy-to-Buy)

Director of Business Development

PMO Programme Manager

Security & IT Manager

Medior Change Consultant

Senior Strategy & Transformation Officer | Open Bank, S.A., Netherlands Branch

Business Development Manager - Export Europe (all genders)

Portfolio Manager

Requirements Engineer (Medewerker Requirements)

Digital Program Manager – Commercial Growth

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van program manager in amersfoort, ut

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