Science with Purpose.
Work with Impact.
At MediWound, we are pioneering next-generation enzymatic therapies that transform the science of wound care. Our people are the foundation of our innovation — passionate scientists, clinicians, and professionals committed to advancing patient care through biotechnology.
As a global biotech company, MediWound offers opportunities to grow across research and development, clinical operations, manufacturing, regulatory affairs, and corporate functions. Here, your work will contribute to breakthrough therapies that improve outcomes for patients worldwide.
This is more than a career — it’s a chance to shape the future of regenerative healing.
Explore our opportunities and take the next step in your biotechnology journey with MediWound.
Open Positions
Medical Director- Medical Safety Monitor
We are seeking a Medical-Safety Monitor to provide medical safety oversight for clinical trials. In this role, you will act as the main medical safety contact for study teams, ensuring subject safety medical data integrity. You will work closely with cross-functional teams under the supervision of the Medical Director, Safety & Pharmacovigilance.
If you’re passionate about advancing patient safety in clinical research, we’d love to hear from you.
Key Responsibilities
- Serve as the medical safety expert for assigned trials
- Review and assess safety data (e.g adverse events, serious adverse events, labs, ECGs, vitals)
- Participate in Safety Review Meetings & be responsible for DMC interactions
- Support safety signal detection and risk assessment
- Provide medical input to study documents and clinical data review
- Collaborate with Clinical Operations, Biostatistics, Regulatory & Pharmacovigilance teams
Qualifications
- MD degree
- 4+ years experience in clinical research, medical or safety roles
- Excellent communication skills in English
Preferred
- Experience in pharmacovigilance and safety evaluation
- Experience in clinical data interpretation
Come work with us
Medical Director- Medical Safety Monitor
JB-225
Automation & Computerized Systems Lead
Summary
Lead and maintain industrial automation (PLC/HMI/SCADA) and enterprise computerized systems (QMS, ERP, LIMS) in a GMP-regulated pharmaceutical environment. Ensure high system reliability, data integrity, and compliance while supporting Production, Engineering, Maintenance, QA, and Validation teams. Drive technical improvements, troubleshoot complex automation issues, and oversee IT/OT integration for seamless and secure operations.
Key Skills & Expertise:
- PLC/HMI/SCADA system ownership and troubleshooting (Siemens, Unitronics, Allen-Bradley, AVEVA/Wonderware)
- Enterprise system management (QMS, LIMS, ERP, maintenance/calibration)
- GMP compliance, data integrity (ALCOA+), and computerized system validation
- Technical support for production machinery, process control, and automation modernization projects
- Collaboration with vendors, contractors, and cross-functional teams