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Projektbeschreibung
Leading medical device company is expanding their regulatory team and are seeking for an interim Regulatory Affairs Associate.
Energetic and progressive medical device company has big plans over the next 12 months and are looking for someone to support their existing regulatory team.
General Responsibilities Include;
- Maintaining and updating technical files.
- Submitting documents to standards within EMEA,
- General regulatory support to existing team.
Key skills;
- 2-3 year's regulatory affairs experience.
- Working experience in a medical device back ground.
- Good technical file understanding.
If you feel that you have the experience necessary, or know someone who has, please contact me Joseph on details below.
To find out more about Real Staffing please visit www.realstaffing.com
Energetic and progressive medical device company has big plans over the next 12 months and are looking for someone to support their existing regulatory team.
General Responsibilities Include;
- Maintaining and updating technical files.
- Submitting documents to standards within EMEA,
- General regulatory support to existing team.
Key skills;
- 2-3 year's regulatory affairs experience.
- Working experience in a medical device back ground.
- Good technical file understanding.
If you feel that you have the experience necessary, or know someone who has, please contact me Joseph on details below.
To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
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Einsatzort:
London, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges