This position will support RA Technical check.
You will be responsible for ensuring compliance of publishing ready documents so that when these documents go for eCTD, NeeS publishing there should not be any showstopper elements. You will also be responsible to check the Published output as per the provided table of contents. Critical check should be done for PDF format, Bookmark information, Hyperlinks, etc.
In addition you are also responsible to support regulatory dossier publishing in eCTD, NeeS, Paper & other national format. The publishing task will be done with the help of software dedicated for publishing.
Qualifications
Relevant academic degree at minimum masters level in life sciences eg. Master of Pharmacy, Master of Sciences. Professional skills include working knowledge in PDF reader & PDF writer; strong ISI Tool & Adobe Acrobat knowledge (MS Office applications); working knowledge in eCTD publishing tool & experienced in dossier compilation. 1 to 2 years of experience in regulatory dossier compilation is mandatory.
Proficiency in oral and written English is essential. The job requires cultural awareness and the ability to communicate with stakeholders with diverse cultural backgrounds.
“At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.”
Contact
For further information please contact Surajit Roy on +91 9591996412.
Deadline: 11 July 2014
Read More
You will be responsible for ensuring compliance of publishing ready documents so that when these documents go for eCTD, NeeS publishing there should not be any showstopper elements. You will also be responsible to check the Published output as per the provided table of contents. Critical check should be done for PDF format, Bookmark information, Hyperlinks, etc.
In addition you are also responsible to support regulatory dossier publishing in eCTD, NeeS, Paper & other national format. The publishing task will be done with the help of software dedicated for publishing.
Qualifications
Relevant academic degree at minimum masters level in life sciences eg. Master of Pharmacy, Master of Sciences. Professional skills include working knowledge in PDF reader & PDF writer; strong ISI Tool & Adobe Acrobat knowledge (MS Office applications); working knowledge in eCTD publishing tool & experienced in dossier compilation. 1 to 2 years of experience in regulatory dossier compilation is mandatory.
Proficiency in oral and written English is essential. The job requires cultural awareness and the ability to communicate with stakeholders with diverse cultural backgrounds.
“At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.”
Contact
For further information please contact Surajit Roy on +91 9591996412.
Deadline: 11 July 2014
Read More
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