Global Labeling Proofreader to AstraZeneca
Adecco Sweden AB / Administratörsjobb / Göteborg
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hela Sverige At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people 's exceptional skills with those of people from all over the globe.
We now have the opportunity for one consultant to join our team in the role as a Global Labeling Proofreader. 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.
This is a temporary position for 12 months starting in July.
Major Duties and Responsibilities
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 Requirements
• 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.
About the employment
For this assignment, you will be employed as a consultant by Adecco. The assignment will start in July and initially run for 12 months.
Adecco adheres to all relevant collective agreements.
Your health and wellbeing are important to us so we offer healthcare benefits, such as discount on training cards. You are also covered by insurance and occupational healthcare.
The Adecco Group is the worlds leading provider of HR solutions. With more than 32,000 FTE employees and around 5,100 branches, in over 60 countries and territories around the world, we offer a wide variety of services, connecting around 700,000 associates with our clients every day.
The services we offer fall into the broad categories of temporary staffing, permanent placement, career transition and talent development, as well as outsourcing and consulting. The Adecco Group is based in Zurich-Glattbrugg, Switzerland and we are a Fortune Global 500 company listed on the SIX Swiss Exchange.
Adecco was created in 1996, following the merger of Adia (Switzerland) and Ecco (France), two leading personnel service firms with complementary geographical profiles.
Read more at
www.adecco.comAbout the application
The assignment will be filled immediately and we are therefore recruiting on a continuous basis during the application period. Please apply through the "Ansök/Apply" button on this page and attach your CV and personal letter.
* The first step in our recruitment processes is a personality test (MAP) that will be sent to your e-mail address when your application has been reviewed. Adecco uses tests as part of the process in order insure quality and to make as fair an assessment as possible.
* If you are selected to continue to the next step in the process, you will be contacted for a telephone interview.
* The next step will be to attend a personal interview with the responsible recruiter.
Please note that in some of our processes we also use video interviews, other tests and other assessment techniques. If this is the case, you will receive information.
Contact details
If you have questions about this assignment or the recruitment process,
you are welcome to contact responsible recruiter:
Isabell Josefsson via +468 - 100 500
If you have questions regarding registration with Adecco,
please contact Adecco Candidate Support:
kandidatsupport@adecco.se alt. via tel: +468 - 598 980 10.
We look forward to receiving your application!
Keywords
Proofreader, Korrekturläsare, Författare, Engelska, Göteborg, Mölndal, AstraZeneca, Adecco
Varaktighet, arbetstid
Heltid Visstid
Publiceringsdatum2018-05-23ErsättningFast lön
Så ansöker duSista dag att ansöka är 2018-06-22
Klicka på denna länk för att göra din ansökanKontaktIsabell Josefsson
Isabell.Josefsson@adecco.seFöretagAdecco Sweden AB
AdressAdecco Sweden AB
Östra Hamngatan 26-28
41109 GÖTEBORG
KontorsadressÖstra Hamngatan 26-28
Jobbnummer 4161096
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