Operations Quality Engineer to Oticon Medical
Oticon Medical AB / Övriga jobb / Göteborg
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hela Sverige Visa alla jobb hos Oticon Medical AB i Göteborg We put people first! Our mission is clear: We want hearing impaired to be able to experience the sounds of life. This is the foundation for everything we do - which drives us and keeps us focussed on innovation efficacy. We want to develop the world's best hearing healthcare solutions.
Would you like to work with products that actually change the lives of people worldwide and do it in a fast-growing company? Then we can offer you an exciting opportunity in Oticon Medical.
Right now, we are looking for a dedicated and highly skilled Operations Quality Engineer to support our fast-growing business and international expansion.
Bone Anchored Hearing Systems
The job we offer you will play an important part of ensuring to keep our products on the market! Team wise, you can look forward to joining the Operations team consisting of 7 dedicated and highly skilled colleagues. The team is responsible for all manufacturing and logistics activities as well as maintenance of all products released to market. Besides your closest colleagues you will be working closely with the other functions in the company and our external partners.
Core responsibilities
You contribute to set-up and maintenance of efficient and secure manufacturing and logistics flow through outsourced processes.
The position is situated in our Gothenburg office working with Bone Anchored Hearing Systems (BAHS). In your new job, you will be working with activities and projects related to our outsourced manufacturing and distribution processes.
Assignments could include;
• set-up of manufacturing processes in collaboration with our suppliers as part of product development projects
• supplier change projects
• projects related to distribution and return flows.
The work includes ensuring quality of our processes and that activities are defined, planned, documented and executed according to Medical Device standards and regulations, all in collaboration with internal and external partners.
What we are hoping for
We are looking for someone with a passion to work with manufacturing and logistics processes; set-up, maintenance and improvements.
What you bring:
• B.Sc. / M.Sc. in Engineering or similar relevant background
• We prefer that you have experience from process validation and supplier quality from the medical device industry, GMP and ISO 13485.
• You are stimulated by building relationships and implementing improvements and new processes as well as working in cross functional teams with your colleagues.
Your professional style is characterized by your ability to work structured and focused in a technical and professional manner
Besides that, we expect that you are pragmatic and strive for efficiency in all that you do. You have a holistic view of thinking and acting and are driven by taking responsibility.
Besides the above mentioned, we prefer flexible candidates who can travel up to 40 days per year.
We believe in the good life
We create solutions that allow people to live their lives to the max! We also recognize that in order to bring energy and inspiration to work, you need to re-energize and spend time with family, friends and hobbies in a healthy work life balance. We offer you professional and personal development opportunities.
The atmosphere is informal and creative where respect is pivotal and we strive for the common goal.
Application
To apply for this position please attach your CV and personal letter in English. For more information please contact Karolin Isberg Jernby +46 (0)703-551459
We are looking forward to hearing from you!
Publiceringsdatum2018-08-14Så ansöker duSista dag att ansöka är 2018-09-04
Klicka på denna länk för att göra din ansökanFöretagOTICON MEDICAL AB
KontorsadressEKONOMIVÄGEN 2
Jobbnummer 4289857
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