Our client is a global market leader in medical devices and pharmaceutical product development! They are looking for a Project Manager that would focus on product development activities with regulatory affairs and quality supporting activities for finished products and packaging across medical devices, substance-based devices, and supplements.
*3 days per week home office offered with this position with office located in Saarland!
Responsibilities:
- Development of cosmetic products, food supplements, material medical products, primary packaging in accordance with regulatory requirements that are required for specific countries.
- Creation of product dossiers and assistance with the registration and approval process for medicines and medical devices, particularly with EU MDR.
- A lot of variety and flexibility to work on different projects every week and having a close contact with customers.
- Optimisation of current products throughout the entire product life cycle
- Implementation of technology transfer projects.
- Leadership of QMS improvements and assurance of ISO 13485 compliance.
What is required:
- Degree in Chemistry, Biology, Pharmacy, or similar engineering degree.
- At least 2 years of previous experience in the development of drug-delivery or medical devices.
- Good knowledge of the ISO 13485, QMS, and EU MDR.
- Fluency in English.
- Intermediate German skills (minimum B1 level).
What is offered:
- Friendly and supportive working atmosphere in a motivated and committed team.
- Flat hierarchies with quick decision-making processes and a lot of space for your own creativity.
- Varied tasks in a successful company with an international focus
- Performance-based pay.
- Hybrid working style (2 days in the office, 3 days remote work) .
Please contact Dominika Wyrwinska for more details about this position or to connect about other positions in medical technology.
dominika.wyrwinska@adaptivelifescience.com
#LI-DW1
#LI-Hybrid