Fresenius Kabi

Prepare and file high-quality regulatory submissions while ensuring compliance with cGMP standards. Provide regulatory guidance to project teams and develop strategies for complex issues impacting timelines and costs. Train new regulatory specialists.

The Sr Principal Engineer guides software design and development for medical devices, resolving complex problems and mentoring junior engineers while adhering to medical regulations.

The Senior Engineer, Reliability plans and conducts tests to ensure product reliability in medical devices, maintaining documentation, and collaborating with teams.

The Manager, Quality Assurance Auditor schedules and leads quality audits, identifies compliance risks, prepares reports, and drives corrective actions in a pharmaceutical context.