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Regulatory Affairs Officer for medical device development

Phillips-Medisize is looking for an Regulatory Affairs (RA) Officer for Global Innovation Development EU in Struer, Denmark. If you have a passionate interest in creating unique products for people who need medical treatment and want to be part of a rapidly expanding project organization, you might be the one we are looking for.

About the position:

As RA Officer you will be part of the RA team. The team is responsible for the regulatory approvals in different countries executed either by ourselves or in close cooperation with customers. This product approval process starts early in the product development project phases and continues throughout the product lifetime. Your main responsibilities will be:

  • to participate in medical device development projects to lay out the regulatory strategy 
  • to support regulatory intelligence work so we are always up-to-date on regulatory expectations
  • to execute the agreed regulatory strategies and coordinate regulatory work with customers and authorities
  • perform regular reviews of technical files

The position requires both internal and external cross functional cooperation and communication. 

What we are looking for in you: 

Professional qualificationsMaster or Bachelor degree in Natural Science or similar qualifications. More than 3 years experience as a Design Assurance engineer or Regulary professional – preferably in the medical device industry. 

You also have proven experience/knowledge with:

  • Medical device quality management systems and standards (eg. ISO 13485:2016, MDD and MDR)
  • Preparing Technical File for CE marking, preparing 510(k) package to FDA, preparing Device master File (MAF) to FDA.obtaining and maintaining regulatory approvals
  • Keeping overview of regulatory commitments and driving necessary actions to maintain approvals for systems and products
  • Authority inspections/audits

Personal qualifications

You are analytical and theoretical well-grounded. You have a systematic approach to your work and you deliver well-structured results. You have a holistic can-do attitude, a pro-active approach and deliver on time. You thrive in a changing environment and by working across many disciplines – some of these are probably new to you. You have excellent written and verbal communication skills in English.

We offer you

  • A challenging position in an international innovative and successful company in growth
  • An opportunity to become part of a team of dedicated and highly qualified RA colleagues based in Struer, Denmark
  • Cooperation in cross-functional project teams with great opportunities to influence the daily work 
  • Participation in developing the RA area to support a more global set up and more complex products 
  • Well-structured training and continuous development of your competencies.
  • Flexible working hours
  • Salary on a competitive level

We look forward to hearing from you.

Application

We processes applications continuously. Please submit your application and CV soonest possible from our website.

The Company – in short

Phillips-Medisize A/S is an excellent expert in the design, development and delivery of advanced drug delivery devices and connected health solutions.  Our customers are leading pharmaceutical companies worldwide.Phillips-Medisize A/S is a part of Molex. We offer innovative and integrated solutions supported by an end-to-end service offering from Strategy to Launch. Read more about Phillips-Medisize A/S at www.phillipsmedisize.com or follow us at LinkedIn.


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330152529Phoenix-361ee9ef12020-01-09T00:00:00Regulatory Affairs Officer for medical device development

Phillips-Medisize is looking for an Regulatory Affairs (RA) Officer for Global Innovation Development EU in Struer, Denmark. If you have a passionate interest in creating unique products for people who need medical treatment and want to be part of a rapidly expanding project organization, you might be the one we are looking for.

About the position:

As RA Officer you will be part of the RA team. The team is responsible for the regulatory approvals in different countries executed either by ourselves or in close cooperation with customers. This product approval process starts early in the product development project phases and continues throughout the product lifetime. Your main responsibilities will be:

  • to participate in medical device development projects to lay out the regulatory strategy 
  • to support regulatory intelligence work so we are always up-to-date on regulatory expectations
  • to execute the agreed regulatory strategies and coordinate regulatory work with customers and authorities
  • perform regular reviews of technical files

The position requires both internal and external cross functional cooperation and communication. 

What we are looking for in you: 

Professional qualificationsMaster or Bachelor degree in Natural Science or similar qualifications. More than 3 years experience as a Design Assurance engineer or Regulary professional – preferably in the medical device industry. 

You also have proven experience/knowledge with:

  • Medical device quality management systems and standards (eg. ISO 13485:2016, MDD and MDR)
  • Preparing Technical File for CE marking, preparing 510(k) package to FDA, preparing Device master File (MAF) to FDA.obtaining and maintaining regulatory approvals
  • Keeping overview of regulatory commitments and driving necessary actions to maintain approvals for systems and products
  • Authority inspections/audits

Personal qualifications

You are analytical and theoretical well-grounded. You have a systematic approach to your work and you deliver well-structured results. You have a holistic can-do attitude, a pro-active approach and deliver on time. You thrive in a changing environment and by working across many disciplines – some of these are probably new to you. You have excellent written and verbal communication skills in English.

We offer you

  • A challenging position in an international innovative and successful company in growth
  • An opportunity to become part of a team of dedicated and highly qualified RA colleagues based in Struer, Denmark
  • Cooperation in cross-functional project teams with great opportunities to influence the daily work 
  • Participation in developing the RA area to support a more global set up and more complex products 
  • Well-structured training and continuous development of your competencies.
  • Flexible working hours
  • Salary on a competitive level

We look forward to hearing from you.

Application

We processes applications continuously. Please submit your application and CV soonest possible from our website.

The Company – in short

Phillips-Medisize A/S is an excellent expert in the design, development and delivery of advanced drug delivery devices and connected health solutions.  Our customers are leading pharmaceutical companies worldwide.Phillips-Medisize A/S is a part of Molex. We offer innovative and integrated solutions supported by an end-to-end service offering from Strategy to Launch. Read more about Phillips-Medisize A/S at www.phillipsmedisize.com or follow us at LinkedIn.

2020-02-17T18:50:52.733 Phillips-Medisize is looking for an Regulatory Affairs (RA) Officer for Global Innovation Development EU in Struer, Denmark. If you have a passionate interest in creating unique products for people who need medical treatment and want to be part of a rapidly expanding project organization, you might be the one we are looking for. About the position: As RA Officer you will be part of the RA team. The team is responsible for the regulatory approvals in different countries executed either by ourselves or in close cooperation with customers. This product approval process starts early in the product development project phases and continues throughout the product lifetime. Your main responsibilities will be: to participate in medical device development projects to lay out the regulatory strategy to support regulatory intelligence work so we are always up-to-date on regulatory expectations to execute the agreed regulatory strategies and coordinate regulatory work with customers and authorities perform regular reviews of technical files The position requires both internal and external cross functional cooperation and communication. What we are looking for in you: Professional qualificationsMaster or Bachelor degree in Natural Science or similar qualifications. More than 3 years experience as a Design Assurance engineer or Regulary professional preferably in the medical device industry. You also have proven experience knowledge with: Medical device quality management systems and standards (eg. ISO 13485:2016, MDD and MDR) Preparing Technical File for CE marking, preparing 510(k) package to FDA, preparing Device master File (MAF) to FDA.obtaining and maintaining regulatory approvals Keeping overview of regulatory commitments and driving necessary actions to maintain approvals for systems and products Authority inspections audits Personal qualifications You are analytical and theoretical well-grounded. You have a systematic approach to your work and you deliver well-structured results. You have a holistic can-do attitude, a pro-active approach and deliver on time. You thrive in a changing environment and by working across many disciplines some of these are probably new to you. You have excellent written and verbal communication skills in English. We offer you A challenging position in an international innovative and successful company in growth An opportunity to become part of a team of dedicated and highly qualified RA colleagues based in Struer, Denmark Cooperation in cross-functional project teams with great opportunities to influence the daily work Participation in developing the RA area to support a more global set up and more complex products Well-structured training and continuous development of your competencies. Flexible working hours Salary on a competitive level We look forward to hearing from you. Application We processes applications continuously. Please submit your application and CV soonest possible from our website. The Company in short Phillips-Medisize A S is an excellent expert in the design, development and delivery of advanced drug delivery devices and connected health solutions. Our customers are leading pharmaceutical companies worldwide.Phillips-Medisize A S is a part of Molex. We offer innovative and integrated solutions supported by an end-to-end service offering from Strategy to Launch. Read more about Phillips-Medisize A S at www.phillipsmedisize.com or follow us at LinkedIn.11Jobnet361ee9ef100000000000IDK_OFIR_02DKDanmark228DKK2020-03-03T00:00:000000https://www.phillipsmedisize.com/join-us/europe-careers/regulatory-affairs-officer-for-medical-device-development0EuropaDanmarkJyllandVestjyllandLemvig3688405Phillips-Medisize A/S11Gimsinglundvej 207600StruerDKDanmark0
DKDanmarkDKDanmark
8Fuldtid46Permanent10000880728JobNet5095769509576910007-01-2020000https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=361ee9efhttps://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=361ee9efhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=361ee9ef&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=361ee9ef&page=EmailApplyForm&component=SendApplicationButtonhttps://static.matchwork.com/company/logo/DK/ORS/SoMe/Produktion_haandvaerk_og_transport/Haandvaerk_og_service/1.jpgRegulatory Affairs Officer for medical device development9006001Dansk3Læse/ tale11018Officer7Håndværk & service363891902Applynoreply@ofir.comDKDanmarkDKDanmarkda-DK