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At STADA we pursue our purpose “Caring for people‘s health as a trusted partner” worldwide. Originally founded by pharmacists, we are a leading manufacturer of high-quality pharmaceuticals. More than 12,300 employees around the globe live our values Integrity, Entrepreneurship, Agility and One STADA to achieve ambitious goals and shape the successful future of STADA.

 

Our global headquarters, STADA Arzneimittel AG, is located in Bad Vilbel near Frankfurt am Main.


(Junior) Specialist (f/m/d) Regulatory Submissions Maintenance   

Bad Vilbel | Germany (DE) | Full-time | Permanent 

 

Your responsibilities:

 

- Supporting preparation and submission of maintenance- and life-cycle activities for medicinal products (variations, renewals, PSUR submissions) 

- Project coordination and reporting

- Working in project teams with internal stakeholders and external suppliers

- Preparation, review, revision and maintenance of regulatory documents

- Monitoring of internal and external deadlines

- Administration of data in regulatory databases

 

Your qualification:

 

- Professional education with scientific background or experience in Regulatory Affairs

- Subtancial knowledge of the legal framework for Regulatory Affairs for medicinal products in the EEA

- Ability to work under own responsibility

- Very good communication and social skills

- Strong sense of responsibility

- Structured and result-oriented approach, including a problem-solving attitude

 

We are looking for talents with expert knowledge and an entrepreneurial spirit that enjoy working collaboratively in a global team. We are pleased to get to know you better. Please use our online portal to submit your application: jobs.stada.com

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