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Regulatory Affairs Specialist - Junior, Contract, Switzerland
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Marketing, Engineer
Projektbeschreibung
REGULATORY AFFAIRS MEDICAL DEVICE, SOLOTHURN, CONTRACT, GERMAN
We have an opportunity to join a major medical device company in Solothurn to contribute towards the preparation of any critical regulatory documentation of specified regulatory submissions in accordance to European Medical Device regulations, please note that upper intermediate German speaking (B2+) is essential for the role. The contract is on a full time, onsite 3 month Contract basis and pays an Hourly rate of 80 Chf.
A minimum of 2 years of regulatory affairs experience for the medical device industry is required for the role plus German speaking, you must have a good understanding of European regulations and preferably worked on the 93/42/EEC regulation and experience within a clinical trial programme environment. The role will encompass core responsibilities within regulatory compliance for developing and writing clear arguments and explanations for new product licenses and license renewals. Other responsibilities include regulatory labelling and contribution to quality assurance. If you are a German speaking medical device professional who is available on short notice but do not hold all of the above requirements then please feel free to apply for the position. Please note there is a there is a detailed job description available on request, the job title for the role is 'Regulatory Affairs Specialist'.
We understand that you may wish to know more about the responsibilities of the role before submitting an application, please feel free to submit your CV or contact details via this website or email me on open-link LinkedIn/XING and I will be happy to answer any questions you may have.
We look forward to hearing from you,
Kind regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 109219
Key words: regulatory affairs, RA, medical device, documentation, business development, clinical trial, German, labelling, Packaging, marketing authorization, audits, QA, leaflets, storage, packaging, regulatory submissions, manufacturing, Switzerland, license, CE, 93/42/EEC, Engineer, FDA, Mechanical, Electronic, Ingenieur, Regulatory Compliance,
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
We have an opportunity to join a major medical device company in Solothurn to contribute towards the preparation of any critical regulatory documentation of specified regulatory submissions in accordance to European Medical Device regulations, please note that upper intermediate German speaking (B2+) is essential for the role. The contract is on a full time, onsite 3 month Contract basis and pays an Hourly rate of 80 Chf.
A minimum of 2 years of regulatory affairs experience for the medical device industry is required for the role plus German speaking, you must have a good understanding of European regulations and preferably worked on the 93/42/EEC regulation and experience within a clinical trial programme environment. The role will encompass core responsibilities within regulatory compliance for developing and writing clear arguments and explanations for new product licenses and license renewals. Other responsibilities include regulatory labelling and contribution to quality assurance. If you are a German speaking medical device professional who is available on short notice but do not hold all of the above requirements then please feel free to apply for the position. Please note there is a there is a detailed job description available on request, the job title for the role is 'Regulatory Affairs Specialist'.
We understand that you may wish to know more about the responsibilities of the role before submitting an application, please feel free to submit your CV or contact details via this website or email me on open-link LinkedIn/XING and I will be happy to answer any questions you may have.
We look forward to hearing from you,
Kind regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 109219
Key words: regulatory affairs, RA, medical device, documentation, business development, clinical trial, German, labelling, Packaging, marketing authorization, audits, QA, leaflets, storage, packaging, regulatory submissions, manufacturing, Switzerland, license, CE, 93/42/EEC, Engineer, FDA, Mechanical, Electronic, Ingenieur, Regulatory Compliance,
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Marketing/Vertrieb, Ingenieurwesen/Technik