Information Security Specialist Ledige Stillinger på Auditdata
Auditdata presserende behov efter position for Information Security Specialist. Læs denne jobannonce grundigt før ansøger om jobbet. Der er nogle kvalifikationer, erfaringer og kvalifikationsbehov, at arbejdsgiverne kræver. Er din karriere historie passer disse krav? Sørg for at du forstår den rolle, du søger, og at det er egnet til dine evner og kvalifikationer.
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Information Security Specialist Ledige Stillinger på Auditdata Detaljer Job:
Are you passionate about process quality?
Do you like to work with continuous improvements of business processes?
Do you have experience with ISO 270001 information security management systems and preferable ISO 13485?
Do you want to be a part of a global organisation with high professional standards and a great working environment?
Then we have an exciting job opportunity that may be your next career move.
We are looking for a IT/Information security specialist who will become an expert in our
- ISMS – Information security Management System and QMS
- Medical device Quality management system
Read the job description for the IT / Information Security Specialist here.
How to apply If you are interested in applying for the position, please send your CV and application using the link below as soon as possible and no later than February 15th , 2018 .
Interviews will be held ongoing.
Your CV & application will be treated confidential.
A global job with impact As IT/Information security specialist, you will get a varied working day in a dynamic organisation where you get to influence Auditdata’s processes as well as your own daily tasks and responsibilities. Your key responsibilities will be to:
- Drive business development projects to develop our Quality/Information
Management System and ensure and maintain efficient and lean procedures
- Managing regulatory services and submissions around the world
- Maintain, develop and improve our global processes and structures
- Act as quality system auditor on our sites (expected travel 2 weeks/year)
- Handle creation, disposition, approval and closure of non-conformity
- Process training
- Key interface to our Outsourced IT operation
- You have ambitions to grow in your job and obtain new qualifications and knowledge
Experience with Medical Devices and Quality Assurance To succeed in the job, you need to have a background as engineer or similar and 3+ years of experience with quality assurance (product QA and/or IT QA) in the medical device/IVD or pharma industry – preferably from both the design/development area and to a lesser degree the manufacturing side. In addition, you have experience with writing procedures and QOP’s and a high degree of flair for working with various IT systems.
It is important that you have great cooperation skills and a structured approach to your work. At the same time, you are open-minded and see possibilities even when daily life is dynamic and hectic.
You can work independently, but you also like to work in teams by being a team player. It is natural for you to be analytical, take charge, and be good at prioritering, planning and finalising your tasks as well as being proactive.
Auditdata is a global company and English is our corporate language, which requires that you speak and write English at a high level, Danish are the preferred language in the Danish office.
Contact You can get more information about the job and about Auditdata A/S by contacting Director Corporate QA/RA & IT security, Dan Haugbøl, telephone no. +45 4075 0311.
Auditdata is a Danish company, founded in 1992, with headquarters in Copenhagen, and subsidiaries in the Nordic counties, the UK, the US, and in Ukraine. Auditdata develops and supports management software systems and measurement equipment for audiologists and hearing instrument dispensers.
Our solutions offer hearing care professionals across the world the most complete, user-friendly applications and devices for handling their daily work.
Our ultimate mission is to improve the quality of life for people with a hearing disability.
Our full software production life-cycle is handled by our office in Kiev in cooperation with key capacities at our main office in Copenhagen as well as our offices in the UK and US.