QA/RA Specialist
Raysearch Laboratories Ab (publ) / Datajobb / Stockholm
Observera att sista ansökningsdag har passerat.
Visa alla datajobb i Stockholm,
Solna,
Lidingö,
Sundbyberg,
Danderyd eller i
hela Sverige Visa alla jobb hos Raysearch Laboratories Ab (publ) i Stockholm,
Båstad,
Arvidsjaur eller i
hela Sverige RaySearch Laboratories AB (publ) is a medical technology company developing advanced software solutions for improved radiation therapy of cancer. RaySearch markets the RayStation® treatment planning system to clinics all over the world. In addition, RaySearch?s products are distributed through licensing agreements with leading medical technology companies. To date, 15 products have been launched and RaySearch?s software is used by over 2,500 clinics in more than 65 countries.
There is now a full-time position vacant at our quality department. You will focus on our quality processes, and will work with all departments within the company. RaySearch is expanding rapidly and as the business continues to evolve, your responsibility will be to provide structure and clarity and implement a strategic approach. Through planning and discussions with colleagues and review of documents and records, you will make sure that RaySearch does not loose in efficiency during the expansion, while standards and laws are complied with.
Your role will involve considerable demands on your social skills and integrity. In discussions with specialists in our organization you will be responsible for meeting both regulatory requirements and business requirements. You need to understand the various conditions that apply to our roles and be pragmatic, while you at the same time clearly communicate what regulations must be complied with.
You will be responsible for internal audits, corrective and preventive actions, document management and internal training records. You will further develop methods and tools to streamline and minimize our administration. You will also take part in hosting external audits.
Since the department is small and the work load varies depending on external factors, you are willing to work with a little of each in both the quality and the regulatory field, as necessary.
QUALIFICATIONS
• University degree or equivalent
• 3-5 years of experience
• having maintained and improved a medical device quality management system
• having driven changes and improvements in medical technology
Operations
• You can contribute to designing a complex work flow to meet internal and external requirements
• You can express yourself well in spoken and written English
You need to have great integrity and at the same time be pragmatic. You need to be clear and educational, orderly and capable of managing and structuring information. You can communicate and discuss complex technical work flows and processes in an easily understandable way.
CONTACT
Send your application and CV to:
ansokan@raysearchlabs.com . For more information on this position, contact David Hedfors, Quality and Regulatory Affairs Director, +46 722 366 110.
Varaktighet, arbetstid
Tillsvidare
Heltid
Publiceringsdatum2015-06-03ErsättningFast månads- vecko- eller timlön
Så ansöker duAnsökan kan skickas till e-postadress:
work@raysearchlabs.comFöretagRAYSEARCH LABORATORIES AB (PUBL)
AdressRAYSEARCH LABORATORIES AB (PUBL)
P.O Box 3297
10365 STOCKHOLM
KontorsadressSVEAVÄGEN 44
STOCKHOLM
Övriga kontaktuppgifterTelefonnummer: 08-51053000
E-postadress:
work@raysearchlabs.com Jobbnummer 2322949
Observera att sista ansökningsdag har passerat.