Regulatory affairs administrator Medtronic Maastricht | Maastricht | Fulltime | Manpower Vacaturenr: 38045125

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Regulatory affairs administrator Medtronic Maastricht

Publicatiedatum: 27 oktober 2017
Regio: Limburg
Opleidingsniveau: HBO
Vakgebied: Administratief
Aantal uren per week: 40
Full time/Part time: Fulltime
Client: Medtronic
Salarisindicatie: Loon per maand
€ 2000,00 per maand € 11,56 per uur
Vacaturenummer: V-0010418

Over de functie

Do you have at least a bachelor’s degree in regulation, administration or life science? Do you want to work for world’s biggest company that specializes in medical technology? Are you fluent in English and are you a quick learner with a knack for administration? Then this is the job for you!

Manpower is looking for a regulatory affairs administration assistant for Medtronic in Maastricht

Your work at Medtronic
As radio/telecom regulatory affairs administrator (RF RAS) you will be working in a versatile job. You will be covering  administrative responsibilities of the current RF RAS who goes on maternity leave. In this position you will work with Business Units and expansion teams to follow up submissions already done, to maintain global radio/telecom product certification and compliance sheets. You will interface with other Medtronic functional groups (e.g. Marketing/Sales, Regulatory Affairs, Reliability/Quality engineers) to gather information and documents required to store and maintain RF product technical files as required by applicable radio/telecom certification regulations. This includes radio/telecom regulatory aspects of user manuals and RF compliance labeling.

This is what you’ll be doing on a daily base:

  • Producing and maintaining tracking sheets of projects, like pending RF certifications, submitted applications, approvals, renewals etc.
  • You will perform follow-ups of current process of certifications
  • Communicating with RA EMEA’s clients (the Business units) on the Radio Frequencies Certifications Plans and update accordingly
  • Support the RF RAS Program Manager in the creation of the direct routes in South Saharan countries, and to create country guidelines/recipes for RF certification processes as for example in South Saharan countries in EMEA region, and other regions where RA EMEA supports the Business Units

Over het bedrijf

About your new employer, Medtronic
Together Medtronic and Covidien are working to improve how healthcare addresses the needs of more people, in more ways and in more places around the world. As one company, they can accelerate and advance their ability to create meaningful innovations but they will only succeed with the right people on their team. This is the ideal opportunity to join them, and be part of their commitment to the health of others. They know the combined resources of Medtronic and Covidien will be transformative, creating new methodologies and new opportunities. Whatever your specialty or ambitions, you can make a difference at Medtronic – both in the lives of others and your career. Medtronic is a $27.8b company with 85,000+ employees, in more than 160 countries. 

At their Bakken Research Center in Maastricht, about 220 clinical researchers, scientists and technical engineers cooperate closely with medical specialists in and outside of Europe to develop new, and improve existing therapies in Cardiac Rhythm Disease Management and Cardiovascular Surgery. Their broad range of clinical services, includes international project management, statistical advise, IT support and medical writing, which makes them Medtronic’s authority on clinical research outside of the US.

Working hours
You will be working 40 hours a week during flexible hours.

Why you would want to work as regulatory affairs administrator at Medtronic

  • Gross salary of 2.000 euro per month
  • A travel allowance of 0,19 euro per kilometre (max. 40 km)
  • A fulltime job with 40 hours guaranteed each week
  • A job for 6 months, when you do well you have a chance to prolong this period
  • A chance to work for world’s largest company that specializes in medical technology, a great boost to your CV

Functie eisen

To be the new regulatory affairs administrator it is important you meet the following requirements:

  • You have at least a bachelor (HBO) degree in regulation, administration or life science
  • You have preferably at least 1 year of experience in administration or a related function (not necessary!)
  • Your English is fluent in both writing and speech
  • You are available to work 40 hours a week
  • You are good at administrative work, you learn fast and you are independent
  • Preferably, You live within a range of 25 km from Maastricht, for example in Valkenburg or Geleen
  • You have working knowledge or are willing to learn international radio frequency regulatory requirements, and procedures including details on submissions
  • The ability to learn and comprehend basic principles of RF, physiology and medical device use
Start date vacancy
This vacancy starts at 6 November 2017.

How can you be considered for this job as soon as possible?
  • Apply online through the orange button 'Solliciteer direct'
  • Fill out the questionnaire (you will receive an e-mail within a few minutes after you have applied for the vacancy)
  • Complete this questionnaire as soon as possible so we can take your application into consideration
  • Review of your application based on your resume and further information
  • Is this vacancy, production worker Hoofddorp, still online on the Manpower website? Then you can still apply for the job!
  • For this job, it's important that your resume is up to date. Please make sure that you add an up to date resume during your application

Regulatory affairs administrator Medtronic Maastricht