Global Labeling Proofreader
Varierande / Administratörsjobb / Göteborg
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hela Sverige The 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 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/Regulatory 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.
Start: Asap. The assignment will last at least 12 months.
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.
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 labelling) is highly desirable.
* Experience working in a GMP pharmaceutical environment preferred.
Hur söker jag tjänsten?
Du söker tjänsten via ansökningslänken nedan med registrerat CV. Ansökan kan tyvärr inte göras via e-post.eller brev. Intervju och anställningsprocess sker löpande. För frågor är du välkommen att kontakta konsultchef Daniella Ravanpå mejladress: .
Du är även varmt välkommen att kontakta mig på LinkedIn genom att klicka på bilden nedan eller följa länken:
https://www.linkedin.com/in/daniellaravan/Varaktighet, arbetstid
Heltid Temporary
Publiceringsdatum2017-08-01ErsättningEj angivet
Så ansöker duSista dag att ansöka är 2017-08-28
Ange följande referens när du ansöker: 27900
Klicka på denna länk för att göra din ansökanKontaktDaniella Ravan
daniella.ravan@manpower.seFöretagVarierande
AdressVarierande
41104
41104 1480
Kontorsadresslilla bommen 5a
Jobbnummer 3622154
Observera att sista ansökningsdag har passerat.