Mölnlycke Health Care seeks experienced Regulatory Affairs in Me
Manpower Professional / Biomedicinjobb / Göteborg
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hela Sverige Mölnlycke Health Care is a world leading manufacturer of single-use surgical and wound care products and services for the professional health care sector.
The Wound Care division offers gentle and effective wound healing and provides a range of unique products based on a patented soft silicone technology, together with surgical, absorbent and fixation dressings.
Mölnlycke Health Care started operations as an independent company in 1998 and was acquired from Apax Partners by Investor in January 2007.
The company has about 5500 employees and manufacturing plants in Belgium, the Czech Republic, Finland, Malaysia, Thailand and the U.K.
Go to
www.molnlycke.com for more company information.
The Regulatory Affairs Europe team is a mixture of qualified and new staff and currently manages all pre-market Regulatory activities across Europe, gives support to R&D project and performing the central complaint handling.
Job description
Location: Göteborg, Sweden
Status: Full-Time Employee
Reporting to the Regulatory Affairs Manager Europe, the Team Leader will actively support and participate in the development of the Regulatory Affairs Europe team in Gothenburg as well as performing operative work in R&D projects. The Team Leader will be involved in the daily activities and in some extent also the overall and long term planning.
The key priorities of the position will include:
• Working closely with colleagues and make a strong contribution to the regulatory work, especially for the Wound Care division.
• Review systems and processes, introduce changes to meet the needs of the growing company, to improve sophistication, efficiency and business alignment.
Requirements
We are looking for a team player with a structured working approach but who also is able to work independent with own initiatives. You should also have good communication skills and simultaneous capability.
The successful candidate has a university degree in life science, such as biochemistry, cell biology, microbiology or pharmacology.
You should have at least 3-5 years experience of qualified regulatory work with medical devices and a good understanding of regulatory requirements in EU, USA and Japan. It is also necessary to have experience from all classes of devices and combination products (medical device supported by a medicinal or biological active component).
It is beneficial to have some background from Quality Assurance and experience of managerial tasks.
Fluency in English is a requirement.
Contact person
For more information about the job position please contact Recruitment Consultant Jeacline Hedlund at +46(0)31-63 15 21 or
jehedl@manpower.se . As the recruitment process is ongoing, we would appreciate your application submitted as soon as possible, however no later than 9 June 2008.
Apply by clicking "Ansök" below.
Publiceringsdatum2008-06-02Arbetstider och omfattningEnligt överenskommelse
ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2008-06-02
Ansökan sker via företagets webbplats.
KontaktJeacline Hedlund
FöretagManpower Professional
AdressManpower Professional
Jobbnummer 239264
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