AstraZeneca is looking for a Regulatory Affairs Assistant
Jurek Rekrytering & Bemanning AB / Administratörsjobb / Göteborg
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hela Sverige Publiceringsdatum2014-08-08Dina arbetsuppgifterThe Global Labeling Operations team is responsible for the regulatory role as part of the process for coordination, development and implementation of new and revised printed labeling for assigned commercial products.
The Labeling Operations Proofreader/Reg Assistant is responsible for supporting development and implementation of new and revised printed labeling for assigned products, primarily in a proofreading capacity. Depending on ability, the candidate may also provide other operational support to ensure labeling document integrity and delivery.
Under the direction of Labeling personnel, responsibilities may include:
• Contribute to labeling submissions for US and EU, including QC, proofing, copy editing and formatting of documents
• Ensure proper version control and document integrity of packaging component labeling, printed labeling artworks and other assigned labeling documents.
• As requested, assist in maintaining repository of current labeling documents and with uploading of documents to electronic document management system.
• Review product labeling galley proofs for the Physician's Desk Reference, as appropriate.
• As requested, participate in the development and maintenance of work practices, templates, and associated documents relating to the labeling function.
Vem är du?
Essential Education, Qualifications, Skills and Experience
• Bachelor's Degree or equivalent experience
• Experience in a proofreading capacity
• Able to multi-task
• Excellent planning and organizational skills
• Excellent oral and written communication skills in English
• Self-motivated and proactive worker
• Proficiency in the use of Microsoft Word, Excel, Project, Adobe Acrobat and other software programs
• Capable of working collaboratively with colleagues in all functions. Team player
• Exercise good judgment and operate with large degree of independence regarding routine assignments
• Cultural Awareness - able to work successfully in a multi-cultural environment
Desirable
• Work experience in a biotech/pharmaceutical arena (preferably in labeling) is highly desirable.
• Experience working in a GMP pharmaceutical environment preferred.
Du erbjuds
You will find yourself in an innovative and creative workplace. For this assignment you have to be available from the first of september and six months ahead. You will be working as a consultant for Jurek Rekrytering & Bemanning at AstraZenecas office in Mölndal. For additional information contact Susanna Filipsson at
susanna.filipsson@jurekbemanning.se . I am looking forward to see your application, please visit us at
www.jurekbemanning.se .
Om företagetAstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration.
Arbetstider och omfattningHeltid Visstidsanställning
ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2014-08-13
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Klicka på denna länk för att göra din ansökanKontaktSusanna Filipsson
FöretagJurek Rekrytering & Bemanning AB
AdressJurek Rekrytering & Bemanning AB
Biblioteksgatan 11
11146 Stockholm
KontorsadressBiblioteksgatan 11, Stockholm
Jobbnummer 1957265
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