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Packaging Developer

  • Mölnlycke Health Care
  • Gothenburg
  • Publicerad: 27 november, 2018
  • Fulltid

 

Do you have what it takes to make a difference?

If the answer is yes, welcome to join us! In our daily work, we create unique medical solutions to improve quality of life. We enjoy what we do because it makes a difference in people’s lives – for real.

Although we’re a global company, we’re still small enough for you to make your mark. Our leaders are accessible and trust us to make the right decisions. As a Mölnlycke employee, you’ll thrive when you take on the responsibility.

We’re now looking for a Packaging Developer to play a critical role in our Packaging and Artwork team. What makes you stand out is your passion for what your work means – coupled with your ability to listen to customers and respond with appropriate urgency.

 

Packaging Developer

As a packaging developer in our packaging and Artwork team you are responsible to secure implementation of new and/or improved packaging solutions for all global products and our evidence-based documentation is compliant. You represent the profession in our Life Cycle Management projects.

 

Your role

  • Secure implementation of new or improved packaging solutions to be completed with all required technical documentation.
  • Maintaining specifications and secure daily operations related to supply and quality
  • Support continuous packaging improvements to improve customer satisfaction and compliance towards regulations in Life Cycle Management projects
  • Accountable to establish and maintain appointed suppliers of raw materials and lead technical aspects during discussions and negotiations and audits with them.
  • Act as a speaking partner to procurement in packaging issues.
  • Support cross functional global projects
  • Contribute to our overall R&D excellence ambition.

 

Qualifications

  • Academic background or equivalent education in related areas
  • Experience in Life Science Industry with focus in Product/Material/Packaging development
  • Experience from working with external suppliers/partners.
  • Ability to handle complex documentation.
  • Good team-working and communication skills.
  • Experience in regulatory requirements and standards for medical devices, e.g. MDR, FDA is desirable.

 

To be successful you have a high degree of customer focus and a business-oriented mindset. You are used to perform with high quality within deadlines. It is essential having a good ability to structure and prioritize, as you will be involved in several cross-functional projects at various stages of development.

This is a full-time permanent position based in Gothenburg.

We look forward to receiving your application. Please send your CV and cover letter to katarina.wanderydz@molnlycke.com

Closing date for applications is 12 December

Questions regarding this position: contact Tom Bergqvist, In-house Recruitment Partner at tom.bergqvist@molnlycke.com or +46 (0)733 – 87272

 

Mölnlycke processes your information for the purpose of considering your application for a position. Please ensure that you have read the our job applicant privacy notice before submitting your resume to us.

 

 

 

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