Process Consultant – Medical Technology | GR Frankfurt | hybrid

Responsibilities

• Analysis and optimization of regulatory processes and contract structures
• Execution of gap analyses of existing processes, interfaces, and contracts
• Assessment of process and contract conformity with applicable medical device regulations
• Development of regulatory-compliant process and contract concepts
• Technical consulting on contract design and contract negotiations
• Coordination with specialist departments and relevant stakeholders
• Conception and evaluation of effectiveness checks of completed audit measures
• Creation of analyses, status reports, and recommendations for action

Requirements

Utilization: 30 %

Do you have time and interest in an exciting project?

Then we look forward to hearing from you!

Contact:

Julia Barth

Expert Candidate Relations

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Constaff GmbH - 100%OpenBook. Honest. Competent. Transparent.

• Several years of experience in quality and process management in regulated industries, particularly medical technology or pharmaceuticals
• Sound knowledge of ISO 13485
• Experience in the evaluation and design of regulatory-relevant contract structures
• Knowledge of international sales and supply chain processes
• Knowledge of South African medical device regulations, especially the Medicines and Related Substances Act 101 and Regulations No. 1515
• Experience with gap analyses, process optimization, and audit measures
• Very good German and English language skills, both written and spoken

Project details

November 2026

3 months

GR Frankfurt / hybrid

Utilization: 30 %

Project ID: 15153

Application deadline: 06.11.2026

Dear Network,

for our client in GR Frankfurt, we are looking for a Process Consultant – Medical Technology.

• Start: 2026-11
• Duration: 3 Monate
• Remote: hybrid
• Location: Frankfurt, Deutschland, DE
• Languages: German