Specialist Medical Regulatory Writing - Stuttgart, Deutschland - Wörwag Pharma GmbH & Co. KG

Wörwag Pharma GmbH & Co. KG

Geprüftes Unternehmen

Stuttgart, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Wörwag Pharma - a medium-sized, internationally active, family-owned pharmaceutical company headquartered in Böblingen near Stuttgart, Germany, which recognized and scientifically proved the importance of biofactors very early on. For more than 50 years, we have been fighting the civilization diseases of our time - preventive, accompanying, healing. Our slogan "Getting closer helping better" is not just a promise to doctors, pharmacists and patients. It is an expression of our colorful corporate culture and our collegial cooperation among our now 1,200 employees worldwide.

Become a part of our team in our headquarter in Böblingen (near Stuttgart) because we are looking for you as a

Specialist Medical Regulatory Writing (M/F/x) (on part time basis / 24 h per week)

Independently work out prerequisites which have to be fulfilled to implement the task (including coordination with IT, RA, process management, own department and within GMA)
Independently discuss technical requirements (IT, Deficiency Letters, Process-Mgmt)
Independent process elaboration and development of a solution including its workflows
Coordination of Data Management and Quality Management
Development of the literature database
Research of scientific literature and integration into a literature database
Transfer of selected data from the literature database into a regulatory database
Consultation / support with / training on Data management systemrelevant questions from/of colleagues
Collaboration in the knowledge database/literature exchange project
Communication with external service providers and vendors
Providing the literature of the dossiers for Regulatory submissions
Creation of a planning tool for internal work plan of Global Medical Writing team
Maintenance of medical and professional information regarding medicoscientific relevant points e.g. originator review
Project management
Education or comparable experience in healthcare industry/ pharmacy counter or similar e.g. nurse, PTA, MTA.
IT background and/or affinity with IT tasks
Basic understanding of medical and scientific terminology
Experience with literature research and handling of literature databases an advantage
Confident handling of MS-Office and extended knowledge MS Excel
Basic knowledge of databases/models
Strong technical and scientific understanding as well as analytical skills
Structured, independent, problemsolving and careful way of working
Very good written and spoken German and English skills
Very good organizational and communication skills
A dynamic, international environment with the opportunity to take on responsibility quickly and extensively, to contribute experience and knowledge and to implement ideas
Varied challenges, as well as exciting projects with a strong team spirit
Compensation in line with the market and your performance, as well as additional benefits which can be used flexibly according to your needs, e.g.,
Subsidy for direct insurance
Individual compensation options for days off, pension provisions or payout
Bonago vouchers for special occasions
Support for your general wellbeing and/or worklife balance
Healthpromoting measures such as discounted conditions on overthecounter (OTC) pharmacy products or health days
Flexible trust working hours (24 hours / week) as well as the possibility to work mobile up to 75% of your working time
Central company headquarters with good public transport connections, as well as mobility allowances
A wide range of opportunities for personal and professional development
Regular employee events