Part-Time&Flexibility - GRA New Products - Wiesbaden Area

What you will enjoy:

• Part-Time Role (About 30 weekly hours) & flexible working time, through which you will easily reach your work-life balance. Part-Time positions are quite rare but this company is already used to the part-time solutions, as some of the 13 firm's registration managers are already working less than 40 hours. Do not miss out this rare opportunity: Get in touch today for more information about!
• You will never get bored at this job, as a consistent part of your agenda is made by development projects. Therefore, you will daily put in place different skills, whilst you further extend your scientific and regulatory knowledge and every day will look different.
• Several training&development opportunities.

Your Key-Tasks:

• Evaluation of the relevant documentation from QS, Clinical and Medical department, in order to structure a solide global registration strategy
• Regular contact to the relevant Health Authorities
• Development of a robust, business sounded CMC regulatory strategy
• Cross-functional cooperation with the sight of adjusting and performing the drug submission plan
• Composition of the relevant regulatory documentation
• Supporting the company´s partners abroad

Location: You can easily reach the company´s site from both Wiesbaden or Frankfurt

Starting Date: To be agreed according to your notice period

Contract Type: Unlimited permanent role

Your Requirements:

• Solid drug or API registration experience with the modules 2.3 and 3
• German language skills on business level are mandatory

My Contact Details:

i-Pharm Consulting

Dr Emma Fleury, Practice Manager für Recruitment in Regulatory Affairs

efleury@i-pharmconsulting.com

TEL: +49 89 3803 5861

Due to the high number of applications, we will not come back to you, if your requirements are too distant from the one requested above. We thank you in advance for your understanding.