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
Validation Manager
We are looking for Validation Manager is responsible for hands-on management and execution of all validation and calibration activities at the manufacturing site. This is a highly hands-on role that involves direct execution of validation activities in the field, authoring and approving validation documentation, close daily interaction with production, labs and engineering teams, and professional management of external contractors and vendors.
The role requires high independence, strong ownership, and end-to-end responsibility, from planning through execution and final reporting.
Hands-On Validation Execution
- Plan, execute, and approve validation activities for equipment, systems, and manufacturing processes
- Perform hands-on IQ / OQ / PQ activities on the manufacturing floor
- Validate:
- Manufacturing and packaging equipment
- Utilities (HVAC, water systems, compressed air, gases)
- Cleanrooms
- Labs equipment’s
- Computerized systems (CSV – as applicable)
- Support equipment installation, FAT / SAT, and introduction of new equipment
Documentation and Compliance
- Hands-on authoring of:
- Validation protocols
- Validation reports
- Risk assessments (FMEA)
- SOPs
- Review and approve validation and quality documentation
- Own, maintain, and update the Validation Master Plan (VMP)
Shop Floor & Manufacturing Support
- High level of presence on the manufacturing floor
- Ongoing support to production during changes, deviations, and troubleshooting
- Analysis of processes, yields, and statistical data
- Support technology transfer and New Product Introduction (NPI) from development to commercial manufacturing
Contractors and Vendors Management
- Hands-on professional management of validation and calibration contractors
- Direct interaction with equipment suppliers, service providers, and external laboratories
- Review and control of contractors’ execution quality and deliverables
Quality & Regulatory Activities
- Manage deviations, investigations, and CAPAs related to validation
- Lead Change Controls associated with equipment and processes
- Prepare for and actively participate in regulatory inspections (FDA, EMA, internal audits)
Education & Experience
- BSc in Engineering, Life Sciences, or a related field – mandatory
- Minimum of 5 years of hands-on validation experience in a GMP environment – mandatory
- Proven experience performing validations directly (not only managing)
Technical Expertise
- Strong knowledge of GMP and pharmaceutical regulatory requirements
- Full understanding of the validation lifecycle
- Experience with manufacturing equipment, utilities, and production systems
Personal Skills
- Strong hands-on mentality and willingness to execute independently
- High level of initiative, ownership, and accountability
- Ability to work independently in a fast-paced, multi-task environment
- Excellent interpersonal and cross-functional communication skills
Languages
- English – high level of reading and writing (mandatory)
- Hebrew – high level
Come work with us
Validation Manager
JB-229
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 & PharmacovigilanceV 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 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