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
Maintenance Employee
| We are looking for a skilled Maintenance Technician to join our team. The role includes performing maintenance and troubleshooting on production equipment and infrastructure in accordance with approved work procedures and required documentation. The technician will be responsible for monitoring and reporting anomalies, conducting preventive maintenance, and handling real-time malfunctions. In addition, the role involves communication with external service contractors to ensure proper execution of maintenance activities. This position requires strong technical understanding, attention to detail, and the ability to work in a regulated environment. |
| • Perform maintenance and troubleshooting of production equipment and utilities in compliance with approved SOPs and documentation.
• Monitor and report any deviations to the Maintenance Manager, completing relevant deviation forms as required. • Execute all maintenance activities, including preventive maintenance and troubleshooting of breakdowns. • Perform periodic monitoring of equipment and utilities to ensure optimal performance. • Establish and maintain communication with external service subcontractors to ensure proper execution of maintenance tasks. *Availability for on-call duties, including nights and weekends.
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| Requirements |
| • At least 2 years of experience in maintenance roles within the pharmaceutical industry.
• Proven experience in maintaining and troubleshooting production machinery and utilities. • Strong understanding of HVAC systems is mandatory. • Knowledge of treated water systems (WFI, PW, RO) is an advantage. • Technical English proficiency for reading and interpreting documentation. • Availability for on-call rotations, including nights and weekends. This role demands a skilled and detail-oriented professional capable of ensuring the reliability, efficiency, and compliance of critical equipment and utilities in a regulated environment. |
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Maintenance Employee
JB-4
Regulatory Affairs Project Manager - Maternity Leave Replacement
We are looking for a highly organized and detail-oriented Regulatory Affairs Project Manager to join our team as a Maternity Leave Replacement.
The ideal candidate will have proven experience in regulatory operations within the pharmaceutical or biotech industry, strong project management skills, and the ability to work independently in a fast-paced, deadline-driven environment. We are seeking a collaborative team player with excellent communication skills, a deep understanding of global regulatory requirements, and hands-on experience with regulatory information management systems (preferably Veeva Vault).
- Lead the planning, preparation, formatting, publishing coordination, and timely submission of global regulatory documents, including initial applications, variations, renewals, responses to Health Authority questions, and other regulatory communications.
- Track submission timelines and deliverables to ensure on-time execution of regulatory projects.
- Ensure that submissions performed by MediWound, comply with current global regulatory requirements and Health Authority guidance documents.
- Serve as the system owner for Veeva Vault RIM, managing all aspects of the system including data governance, user access and training.
- Ensure accurate and timely maintenance of product registration data, submission records, Health Authority correspondence, and regulatory commitments in Veeva RIM.
- Lead continuous improvement initiatives and support ongoing use of Veeva RIM by RS team members.
- Develop and maintain procedures and best practices for document and data management in alignment with regulatory and internal requirements.
- Lead and coordinate all regulatory activities in ROW countries.
- Manage external vendors and service providers supporting regulatory operations and ROW submissions.
- Support audits and inspections by providing documentation and system data as needed.
- Establish and maintain the company publication database
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Regulatory Affairs Project Manager - Maternity Leave Replacement
JB-5
Production Operator
Join our pharmaceutical manufacturing team as a Production Operator! In this role, you’ll operate machinery, uphold quality standards, and help maintain a safe production environment. If you have experience in production operations and a strong commitment to safety and procedure, this is a fantastic opportunity to make an impact in a crucial position. Ready to be part of a team focused on quality and excellence? Apply now!
- Perform production tasks following standard operating procedures (SOPs) in a pharmaceutical manufacturing setting
- Operate and monitor equipment to ensure efficient, safe, and compliant production processes
- Accurately document production activities, maintaining detailed and complete batch records
- Collaborate with cross-functional teams to achieve production targets and address process-related issues
- Adhere to all safety protocols and participate in ongoing training to ensure a safe work environment
- Maintain cleanliness and organization in the production area, including routine cleaning tasks
- High school diploma required; technical certifications are a plus
- Minimum of 2 years’ experience in pharmaceutical, medical device, or food manufacturing (required)
- Clean room experience is a significant advantage
- Proficient in technical English (reading and writing) – mandatory
- Strong work ethic, responsibility, patience, attention to detail, and teamwork skills
- Full-time availability with flexibility for additional hours (no shift work)
- Proactive approach and a strong commitment to quality and accuracy