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Junior Regulatory Affairs Specialist
Eingestellt von Michael Bailey Associates - Munich
Projektbeschreibung
REGULATORY AFFAIRS SPECIALIST - JUNIOR
FUNCTION:
Drawing on relevant expertise and information from both internal and external sources, make a major contribution towards the preparation of any critical regulatory documentation
RESPONSIBILITIES:
- Ensuring that the company's products comply with the regulations
- Keeping abreast of international legislation, guidelines and customer practices
- Collecting and collating a wide range of information
- Developing and writing clear arguments and explanations for new product licenses and license renewals, product labels and patient information leaflets
- life cycle Management
- Update of technical documentation
- Understanding and evaluating complex information
- Advising scientists and manufacturers on regulatory requirements
- Preparing and coordinating documentation
- Maintaining quality systems.
REQUIREMENTS:
- Proven expertise of Medical Device Regulatory Affairs
- Be able to demonstrate driving partnerships within the industry
- Excellent attention to detail
- Excellent communicator, both verbal and written
- More than excellent command of English, German fluent
- Quick learner, motivated self-starter
- Excellent customer service, interpersonal, communication and team collaboration skills
OTHERS:
Contract type: Temporary
Location: Kanton Basel-Land
Start date: 16/06/14
End date: 31/12/14
Weekly hours: 40Michael Bailey International is acting as an Employment Business in relation to this vacancy.
FUNCTION:
Drawing on relevant expertise and information from both internal and external sources, make a major contribution towards the preparation of any critical regulatory documentation
RESPONSIBILITIES:
- Ensuring that the company's products comply with the regulations
- Keeping abreast of international legislation, guidelines and customer practices
- Collecting and collating a wide range of information
- Developing and writing clear arguments and explanations for new product licenses and license renewals, product labels and patient information leaflets
- life cycle Management
- Update of technical documentation
- Understanding and evaluating complex information
- Advising scientists and manufacturers on regulatory requirements
- Preparing and coordinating documentation
- Maintaining quality systems.
REQUIREMENTS:
- Proven expertise of Medical Device Regulatory Affairs
- Be able to demonstrate driving partnerships within the industry
- Excellent attention to detail
- Excellent communicator, both verbal and written
- More than excellent command of English, German fluent
- Quick learner, motivated self-starter
- Excellent customer service, interpersonal, communication and team collaboration skills
OTHERS:
Contract type: Temporary
Location: Kanton Basel-Land
Start date: 16/06/14
End date: 31/12/14
Weekly hours: 40Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges