You will identify funding opportunities, write compelling grant proposals, and manage submission processes to secure research, development, and operational funding. Your ability to research, analyze, and align proposals with organizational goals will be pivotal.

Aufgaben

You will spearhead the implementation of ISO 13485, collaborating with cross-functional teams to establish and document processes that meet regulatory requirements. This includes managing quality management systems, conducting internal audits, and preparing for certification assessments.

Qualifikation

You should have experience in regulatory compliance, technical writing, and grant funding processes, with a proven ability to manage multiple priorities. Knowledge of ISO standards, medical device regulations, and grant agencies is essential.

Benefits

Located in western austria, close to switzerland and southern germany. Above average compensation after time trial, multiple boni, insurance, child care available.

Looking forward to work with you!