AstraZeneca is looking for a Regulatory Affairs Assistant
Manpower Administration Huvudkontor / Administratörsjobb / Göteborg
Observera att sista ansökningsdag har passerat.
Visa alla administratörsjobb i Göteborg,
Mölndal,
Partille,
Kungälv,
Lerum eller i
hela Sverige Visa alla jobb hos Manpower Administration Huvudkontor i Göteborg,
Kungälv,
Borås,
Varberg,
Tranemo eller i
hela Sverige Publiceringsdatum2014-08-12Dina 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.
Vad kan vi erbjuda dig?
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 Manpower at AstraZenecas office in Mölndal.
Kontaktperson för detta jobbFor additional information contact please contact Karin Kvist 031-63 15 97. Apply today!
Arbetstider och omfattning100% Enligt överenskommelse
ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2014-08-13
Klicka på denna länk för att göra din ansökanKontaktKarin Kvist 031-61 72 10
FöretagManpower Administration Huvudkontor
AdressManpower Administration Huvudkontor
Klarabergsgatan 29
11181 Stockholm
KontorsadressKlarabergsgatan 29
Jobbnummer 1959917
Observera att sista ansökningsdag har passerat.