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Regulatory Affairs Specialist - (m/f) - 100%/Medical Devices
Eingestellt von Experis Schweiz AG
Gesuchte Skills: Support, Engineering
Projektbeschreibung
REGULATORY AFFAIRS SPECIALIST - (M/F) - 100%/MEDICAL DEVICES
On behalf of our client, an international and global company, specialized in medical devices based in the Basel area, we are looking for a REGULATORY AFFAIRS SPECIALIST with experience IN THE MEDICAL DEVICES. This is a challenging contracting position starting ASAP until the END OF SEPTEMBER 2016.
As REGULATORY AFFAIRS SPECIALIST you will make sure that the medical devices are compliant with the product development process such as with the applicable regulatory requirements (eg MDD 93/42/EEC). As key team member, you will be responsible for the organization and administration of technical documentation (incl. the update). The Regulatory Affairs Specialist will also be in charge of the evaluation of medical devices regarding risk potential (based on EN ISO 14971). In addition, you will support the international releases of medical devices and prepare and support audits.
IN ORDER TO GIVE THE BEST OUTPUT FOR THE ROLE YOU SHOULD BRING:
- A scientific, medical or ENGINEERING BACKGROUND
- Minimum 3 years' experience in REGULATORY AFFAIRS (incl. MDD 93/42/EEC) of MEDICAL DEVICES (focus on Class I, IIa and IIb)
- Experience with US Regulatory Affairs will be a strong asset
- Excellent communication skills with fluency in GERMAN and ENGLISH
If you are an independent, energetic and highly motivated Regulatory Affairs Specialist who wants to apply your skills in a well-known pharmaceutical environment with very attractive salary and who wants to extend your IT professional network then we look forward to receiving your application!
Do you want to have more information about this exciting role?
Then just give me a call and I will give you all further information about the job and the organization.
You can reach me under the following number (see below)
I am looking forward to hearing from you soon!
We at Experis are carrying out of connecting talent with the right job that helps you in achieving your goals and we understand your needs on what is possible and which opportunities match what you're looking for at the moment. More is humanly possible!
On behalf of our client, an international and global company, specialized in medical devices based in the Basel area, we are looking for a REGULATORY AFFAIRS SPECIALIST with experience IN THE MEDICAL DEVICES. This is a challenging contracting position starting ASAP until the END OF SEPTEMBER 2016.
As REGULATORY AFFAIRS SPECIALIST you will make sure that the medical devices are compliant with the product development process such as with the applicable regulatory requirements (eg MDD 93/42/EEC). As key team member, you will be responsible for the organization and administration of technical documentation (incl. the update). The Regulatory Affairs Specialist will also be in charge of the evaluation of medical devices regarding risk potential (based on EN ISO 14971). In addition, you will support the international releases of medical devices and prepare and support audits.
IN ORDER TO GIVE THE BEST OUTPUT FOR THE ROLE YOU SHOULD BRING:
- A scientific, medical or ENGINEERING BACKGROUND
- Minimum 3 years' experience in REGULATORY AFFAIRS (incl. MDD 93/42/EEC) of MEDICAL DEVICES (focus on Class I, IIa and IIb)
- Experience with US Regulatory Affairs will be a strong asset
- Excellent communication skills with fluency in GERMAN and ENGLISH
If you are an independent, energetic and highly motivated Regulatory Affairs Specialist who wants to apply your skills in a well-known pharmaceutical environment with very attractive salary and who wants to extend your IT professional network then we look forward to receiving your application!
Do you want to have more information about this exciting role?
Then just give me a call and I will give you all further information about the job and the organization.
You can reach me under the following number (see below)
I am looking forward to hearing from you soon!
We at Experis are carrying out of connecting talent with the right job that helps you in achieving your goals and we understand your needs on what is possible and which opportunities match what you're looking for at the moment. More is humanly possible!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges