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Requistion ID : 76287

Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina, USA. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.

Clinical Compliance Manager (m/f/d)

We are looking for a Clinical Compliance Manager (m/f/d) in Constance, Germany for the clinical evaluation. You will prepare clinical evaluations for our restorative and prosthetic products in accordance with EU medical device legislation (MDR) and be responsible for their clinical follow-up (PMCF). Do you enjoy scientific research in medical databases and documentation (systematic literature research)? Then join us and help us to improve dental care in the future!

Key Responsibilities: ​

• Planning, conducting and documenting clinical evaluations (CEP/CER) in accordance with medical device laws and guidelines (MDR, MDCG). The reports reflect the current state of science (SotA).

• Planning and documentation of post-market clinical follow-up (PMCF).

• Planning, performing and documentation of systematic and product-specific literature searches.

• Support PMCF activities for Dentsply Sirona products.

• Contact person for questions regarding safety and efficacy of Dentsply Sirona products and for notified bodies in clinical audits.

• Collaboration with other departments, sites and external consultants.

Requirements and Qualification: ​

• Master's degree in natural sciences, bioengineering or dentistry. You have preferably completed a scientific thesis (PhD or dissertation).

• Several years of experience in the field of clinical evaluation for medical devices, preferably in dentistry.

• Sound knowledge of systematic literature research in the field of medical devices, preferably in dentistry.

• Strong knowledge of medical device legislation and guidelines (MDR, MDCG).

• You can work independently and are a team player with strong communication skills.

• You are also responsible and solution-oriented.

• You are confident with MS Office and medical databases.

• Good language skills in German and English (written and spoken).

What we offer you:

With us, you can expect an attractive salary that recognizes your performance. To enable you to achieve a good work-life balance, we offer 30 days annual leave, flexible working hours and the opportunity to work from home. We also offer an extremely attractive company pension scheme. Furthermore, we promote your further training and development across locations and divisions.