Do you have a passion for the medical technology sector, combined with a strong drive for strategic communication and stakeholder engagement?

We are looking for a Director Investor Relations & Corporate Communications to join our leadership team.

In this role, you will be responsible for ensuring accurate, timely, and compliant communication of the company’s strategic priorities, operational progress, and financial performance to external stakeholders. You will lead all investor relations and corporate communications activities, including digital platforms, and play a key role in strengthening the company’s profile in the financial markets and broader healthcare ecosystem.

You will collaborate closely with the CEO and senior leadership to develop investor-facing materials, manage media engagement, and oversee regulatory-compliant disclosure. The role combines strategic scope with hands-on execution and involves regular interaction with analysts, journalists, and shareholders.

We’re looking for a confident, structured communicator with a scientific background, an understanding of capital markets, and the ability to engage effectively with stakeholders at all levels.

Key Responsibilities

• Develop and implement an investor relations strategy targeting both institutional and retail investors.
• Represent the company in investor meetings, roadshows, and capital markets events across Europe and the US.
• Partner with the CEO to prepare messaging, corporate presentations, and other investor-facing materials.
• Draft and coordinate the release of press announcements, manage investor webcasts, and ensure timely regulatory disclosures.
• Maintain strong relationships with equity research analysts and financial media.
• Oversee investor relations databases and ensure full compliance with FSMA and other financial market regulations.
• Contribute to internal business planning through financial modelling, forecasting, and competitive analysis.
• Manage the company’s ESOP program and ensure internal training on insider information and market conduct rules.
• Corporate Communications.
• Lead external communications and media relations in collaboration with internal teams and external agencies.
• Align messaging with strategic and commercial priorities, and support key corporate announcements and initiatives.
• Work with clinical and external partners to increase visibility of the company’s technology (e.g. alfapump®) in relevant channels.
• Digital & Web Strategy
• Oversee the corporate website and content strategy, working closely with our commercial team and external partners.
• Ensure all online content meets branding, regulatory, and legal standards.
• Evolve digital communications to support engagement with investors, patients, and healthcare professionals.

Key Requirements

• Solid understanding of capital markets and investor communications.
• Excellent written and verbal communication skills; able to convey complex topics clearly and professionally.
• Scientific background with strong financial and analytical capabilities.
• Independent, well-organized, and confident in engaging with internal and external stakeholders.
• Proven experience in managing external communications within a regulated environment.
• Ability to manage multiple priorities and meet strict deadlines with high attention to detail.

Required Education & Experience

• University degree in a relevant discipline. A scientific background is essential.
• Minimum of 3 years of experience in a life sciences company. Additional experience in investor relations, public relations, or investment banking is an asset.
• Fluency in English and Dutch is required.

Join a company at the forefront of medical innovation and contribute to how we communicate our purpose, progress, and priorities to the world!

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Send your CV and full application (in Dutch or English) to careers@sequanamedical.com.
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!

Sequana Medical is a pioneer in medical technology, developing innovative treatments. We’re dedicated to improving lives and making healthcare more sustainable.
Are you a detail-oriented finance professional who enjoys making sure everything adds up, and loves being part of a dynamic, international environment?
Then you could be the person we’re looking for!
We are looking for a hands-on, accurate and motivated part-time AP/AR ACCOUNTANT to join our Finance team at the company headquarters in Ghent. In this key role, you’ll manage both the Accounts Payable and Accounts Receivable processes, helping to ensure our financial operations run smoothly and efficiently.

Key Responsibilities:

• Maintain the AP and AR general ledger for the entire Group
• Ensure proper coding, approval and timely processing of all incoming invoices and employee expense reports
• Review purchase invoices for VAT compliance
• Reconcile vendor statements and follow up on discrepancies
• Prepare payment proposals and execute vendor payments
• Process daily bank transactions
• Monitor and collect outstanding receivables
• Maintain accurate and well-organized filing systems
• Support general accounting tasks

What you bring:

• Bachelor’s degree in Accounting or 2–3 years of relevant experience in an AP/AR role
• Strong Excel skills and experience with accounting software (experience with ERP systems is a plus)
• Solid knowledge of Dutch and English (spoken and written) and strong communication skills
• A keen eye for detail and a proactive, structured working style
• Strong organizational and prioritization skills
• A collaborative mindset and enjoyment in being part of a supportive team across different departments and countries
• Eagerness to learn and grow within the finance function
• Understanding of and commitment to internal control processes

Why join Sequana Medical?

At Sequana Medical, your work has real impact. You’ll be part of a close-knit, international team working on breakthrough medical technologies that improve lives. In this role, you’ll have the opportunity to grow professionally while helping shape efficient, reliable financial processes that support our continued innovation and expansion.

Excited by this opportunity?

Apply now and help us make a difference through innovation in medtech!
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Please note: While we appreciate the interest of recruitment agencies, we kindly ask not to be contacted regarding this position. We do not accept unsolicited candidate introductions or agency services.

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Apply via Linkedin or send your CV and full application (in Dutch or English) to careers@sequanamedical.com.
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!

Sequana Medical is a pioneer in treating fluid overload, a serious and frequent clinical complication in patients with liver disease, heart failure and cancer, when diuretics are no longer effective. alfapump® and DSR® are Sequana Medical’s proprietary approaches that work with the body to remove the excess fluid, delivering major clinical and quality of life benefits for patients and reducing costs for healthcare systems.
We are looking for a technically skilled, hands-on individual to join our small and dynamic manufacturing team in Zurich as a Production Assembler.
As a Production Assembler, you will assemble and test our implantable pump, catheters, and accessories according to defined procedures.
The work is primarily carried out in a clean room, often under a microscope.

Key responsibilities:

• Mechanical assembly of the alfapump® and its subcomponents following defined procedures.
• Operating mechanical and electrical test equipment.
• Packaging and labeling of finished goods.
• Recording manufacturing details in the ERP system.
• Providing technical feedback and support to the Quality Assurance department, including assistance in production audits.

Key requirements:

• Ability to follow detailed technical instructions in English (both oral and written).
• Strong eyesight and fine motor skills.
• Consistently high-quality work, even for repetitive tasks.
• Careful, independent, and precise working style.
• Familiarity with personal computers and standard office software.
• Ability to work both independently and as part of a team.

Required education and professional experience:

• Completed vocational training, such as dental technician, horologist, goldsmith, laboratory assistant, or similar.
• Relevant experience in mechanical assembly of small high-tech devices.
• Experience working with a microscope.
• Experience in a highly regulated production environment (MedTech industry experience is a plus).

Does this opportunity sound exciting?

Join our great team responsible for manufacturing high-tech medical devices that improve quality of life!

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Apply via Linkedin or send your CV and full application (in Dutch or English) to careers@sequanamedical.com.
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!

Are you passionate about advanced electronic systems that make a real impact in the medical technology field?

We are looking for a Medical Device Engineer Electronics to join our Engineering team in Zurich.

In this role, you will act as a subject matter expert in electronics and embedded systems for active implantable medical devices.
You will be responsible for the full life-cycle management of electronic components, from design to performance analysis and verification. You’ll collaborate closely with cross-functional teams, including Regulatory Affairs and Manufacturing, ensuring technical excellence and compliance across the entire product life cycle.
We’re seeking a motivated, detail-oriented professional with strong analytical skills, excellent communication abilities, and a structured, quality-driven mindset.

Key Responsibilities

• Act as the subject matter expert for medical device electronics, embedded systems, and firmware development
• Manage the life-cycle of electronic components in an active implantable medical device system
• Draft and implement change requests related to electronics in coordination with Regulatory and Manufacturing teams
• Create and maintain technical documentation in compliance with the company’s quality management system
• Support the Regulatory and Quality Affairs teams in technical matters
• Perform component verification and technical performance analyses
• Conduct root-cause analysis of returned products and non-conformities in production
• Manage internal and external resources within development projects

Key Requirements

• Proficient in digital and analog circuit design
• Skilled in CAD tools for schematic capture and PCB layout
• Strong analytical and problem-solving skills
• Ability to present complex technical content clearly and in line with regulatory guidance
• Capable of working independently as well as collaboratively within cross-functional teams
• Strong verbal and written communication skills in English
• Highly organized, reliable, and detail-oriented

Required Education / Experience

• Master’s degree in Electrical Engineering or a related field
• Minimum of 5 years R&D experience in a highly regulated industry
• Minimum of 3 years experience in medical device development
• Experience or strong theoretical knowledge in analog and digital signal processing and circuit design
• Experience in firmware development
• Experience with low-power, battery operated embedded systems

Help shape the future of healthcare technology and apply now to join a team dedicated to improving lives through innovation!

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Apply via Linkedin or send your CV and full application (in Dutch or English) to careers@sequanamedical.com.
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!

Are you passionate about driving efficient logistics processes that directly support innovation in medical technology?

We are looking for a Logistics Specialist to join our Manufacturing & Supply Chain team in Zurich.
In this role, you will be responsible for managing inbound and reverse logistics, warehousing, and inventory handling to ensure the smooth flow of materials within our operations. You’ll collaborate closely with Manufacturing, Quality, and Procurement teams to deliver high standards in logistics performance and regulatory compliance.
We’re looking for a proactive and reliable professional with strong organizational and communication skills, who thrives in a highly regulated industry and enjoys contributing to continuous improvement.

Key Responsibilities

• Manage the receipt of purchased and subcontracted materials accurately and on time
• Process returned goods in line with reverse logistics procedures (e.g., RMA process)
• Carry out warehousing tasks including picking and physical storage of goods
• Support the development and implementation of logistics policies and procedures
• Ensure product availability by coordinating logistics flows across departments
• Contribute to operational improvements in logistics performance and efficiency
• Handle import/export shipments in line with relevant trade compliance requirements
• Address customer logistics inquiries and support complaint resolution processes

Key Requirements

• Strong communication and interpersonal skills for effective cross-functional collaboration
• Team-oriented mindset with the ability to work independently and take initiative
• Excellent time management and prioritization skills
• Analytical and process-driven approach to logistics tasks
• Familiarity with ERP systems and logistics-related business processes
• Professional background in logistics and shipping
• Fluent in English and German, both written and spoken
• High attention to detail and a structured way of working
• Willingness to learn and grow within a dynamic environment

Required Education / Experience

• Completed vocational training as a Logistics Specialist or a degree in Logistics, Supply Chain Management, or a related field
• At least 2 years of relevant experience in logistics or supply chain roles
• Hands-on experience with import/export operations and freight forwarding
• Experience in a regulated industry (e.g., Medical Devices, GMP, FDA, ISO 13485) is a strong plus

Contribute to the logistics engine behind impactful healthcare technology. Apply now to become part of a team that values precision, quality, and collaboration!

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Apply via Linkedin or send your CV and full application (in Dutch or English) to careers@sequanamedical.com.
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!

Are you driven by the challenge of transforming cutting-edge product designs into robust and efficient manufacturing processes?

We are looking for a Manufacturing Engineer to join our Manufacturing & Supply Chain team in Zurich.

In this role, you will be responsible for supporting the introduction of new products, optimizing manufacturing processes, and ensuring high standards in quality and efficiency. You will collaborate closely with internal and external stakeholders across engineering, quality, and production to drive improvements and ensure compliance with regulatory requirements.

We are looking for a structured, proactive team player with a solid technical background and a passion for continuous improvement.

Key Responsibilities

• Lead or support internal projects to improve manufacturing operations
• Drive change management activities (CR/CO) and process optimizations
• Support the implementation of new products on existing production lines
• Define new process flows and support design transfer to production or suppliers
• Lead or support CAPAs, NCMRs, and process deviations
• Define, develop, and document manufacturing processes, equipment, and tools
• Create or contribute to User Requirement Specifications (URS) for new assets
• Prepare and maintain manufacturing documentation and ERP/MRP data
• Support validation activities including FAT/SAT, IQ, OQ, PQ, and CSV
• Ensure document compliance within the QMS system
• Interface with suppliers, internal stakeholders, and other company sites
• Identify and drive continuous improvement opportunities
• Maintain a structured, quality-focused approach to scheduling and execution
• Promote a collaborative and GMP-compliant work environment

Key Requirements

• Strong expertise and interest in electronics and mechanical manufacturing operations
• Experience with manufacturing of medical implants is highly desirable
• Skilled in structured problem-solving and process improvement tools (e.g. Six Sigma, 5-Whys, Fishbone)
• Cross-functional mindset with the ability to interact across departments and technical domains
• Strong verbal and written communication skills in both English and German
• Ability to clearly document and present complex technical content
• Self-driven, flexible, and resilient, with a hands-on and analytical working style
• Ability to manage priorities in a dynamic, fast-paced setting
• Knowledge of automation technology is a plus

Required Education / Experience

• Bachelor’s or Master’s degree in Engineering, Science, or a related technical field
• Minimum of 3 years’ experience as a Manufacturing or Process Engineer
• Experience in a regulated environment (e.g., Medical Devices, Pharma, Food) is an asset
• Familiarity with ISO 13485, FDA regulations, and GMP concepts
• Experience with ERP, QMS systems, and CAD tools (e.g., SolidWorks) is a plus
• Proven application of Lean and Six Sigma methodologies
• Proficient with office and technical software

Contribute to the development and production of high-quality medical technology. Apply now and help us shape efficient and reliable manufacturing solutions.

Apply Now!

Does this opportunity sound exciting? Join our dynamic team in Ghent!
Apply via Linkedin or send your CV and full application (in Dutch or English) to careers@sequanamedical.com
Alternatively, you can submit your application via the dedicated form here.
We look forward to hearing from you!