Beschreibung
Regulatory Submission Publisher (m/f/d)
Reference: -en
Start: asap
Duration: 20 MM++
Main tasks:
- Create, assemble and publish electronic submissions per regulatory requirements with a focus on maintenance submissions worldwide (variations, Response to List of Questions etc)
- Coordinates internal publishing activities and liaises with cross functional teams and document authors to assist with timelines and deliverables related to submission documents
- Conducts quality control review tasks
- Publishing, verification, coordination and dispatch of HA compliant, worldwide regulatory submissions
Main qualifications
- Bachelor’s Degree in life sciences or a relevant discipline with profound professional work experience in Pharma or related industry
- Fluent in English (strong oral and written skills
- Familiar with regulatory requirements and good knowledge on regulatory submission format, particularly CTD/eCTD
- Proficiency with MS office and publishing software (e.g. eCTDXpress, DocuBridge, etc.)
Main advantages:
- A highly motivated team and an open way of communication
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Zlatan Mujagic
Referencenumber:
Make contact:
Email: