Grow with us
We are driven to continuously innovate existing medications and offer meaningful benefits to patients, physicians and payors.
Why join us
The key to success is an exceptional workforce. Great people generate great results. As a young, entrepreneurial company, Hyloris fosters creativity, courage, and professionalism.
At Hyloris you will be part of multicultural and multidisciplinary team who will support you to further develop and grow your personal skills.
We strive to create an exciting and dynamic working environment in which you will be challenged to take initiative, contributing to the success of the company.
Interested in joining our mission to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors? Check out our vacancies below.
We look forward to hearing from you.
Latest vacancies
Scientist - Analytical Chemistry
Location: Liege, Belgium
We are currently looking for a Scientist specialized in Analytical Chemistry. The successful candidate will perform pharmaceutical laboratory operations in a start-up environment.
Job description
As a Scientist – Analytical Chemistry your role and responsibilities will be to:
- Perform pharmaceutical laboratory operations in a start-up environment.
- Execute pharmaceutical analytical development work in guidance from Senior Scientist or lab manager or its designee.
- Support new laboratory operations and implement systems and process to ensure compliance & data integrity.
- Collaborate with Hyloris’ team of globally experienced scientists.
- Perform the laboratory activities for analytical development with minimum supervision.
- Participate in development of ongoing & new projects in parenteral and liquid oral dosage forms such as solution, suspension, and solid dosage forms such as oral tablets, capsules dosage form, etc.
Main tasks
- Execute Analytical Test Plans, Specifications, method robustness studies, review or develop analytical method verification protocols, method validation protocols and report, etc.
- Execute the qualification, maintenance, calibration of all instruments and ensure compliance to data integrity.
- Perform standard analytical laboratory tasks such as Karl Fisher water content, Titrimetry, pH and Dissolution testing, etc.
- Carry out and support extensive Pre-formulation studies such as solubility, pH stability profile, compatibility, characterization using advanced analytical techniques such as HPLC, UV, DSC, XRD, PSD, SEM, etc
- Support the development and validation analytical methods using chromatographic (HPLC, GC) and spectroscopic techniques (UV) per ICH, USP, US FDA, EMA requirements.
- Execute laboratory operations, plan, schedule and implement experimental designs.
- Develop and validate analytical methods as per regulatory standards for all products in the pharmaceutical development pipeline based on requirement.
- Execute all experiments and record them in laboratory notebook support in preparation of analytical documents, protocols, study designs, reports.
- Execute pharmaceutical development lab studies, participate in technology transfers, method transfers, method verifications and method validation work in compliance with GMP guidelines.
- Participate in review of Submission Documents for Pre-IND, IND, NDA, as well as Quality GMP documents such as SOP’s, OOS investigations, CAPA, etc.
Your professional profile
- Minimum Qualification: (Professional) Bachelor in Sciences (Chemistry, Pharmaceutical or allied / equivalent).
- Minimum Experience: +3 years industrial experience in pharmaceutical R&D.
- Languages: English [written and verbal] – French is an asset.
- Computer literate: MS office suite, Design Expert software (or equivalent), Basic statistical calculations.
Your abilities
- Demonstrates strong work ethic, and effective written and verbal communication skills.
- Strong analytical/formulation skills, good negotiator/diplomat, enabler.
- Strong interpersonal skills, a collaborative and trust enabling working style, building partnerships among key stakeholders. Good team player.
- Organizational aptitude to be part of an outstanding team.
- Adaptability, flexibility, independence, and resourcefulness to both lead a big vision strategy while also willing to roll-up-sleeves and multi-task to thrive in a growing environment.
- To have essential professional attributes include a detailed-oriented analytical thinking, a team-player attitude, respect and understanding for cultural differences in different countries, and efficient utilization of time and resources.
About Our Company
Hyloris is a specialty biopharma company focused on innovating, reinventing, and optimising existing medications to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors.
Hyloris has built a broad, patented portfolio of reformulated and repurposed value-added medicines that have the potential to offer significant advantages over available alternatives. Two products are currently in initial phases of commercialisation with partners: Sotalol IV for the treatment of atrial fibrillation, and Maxigesic® IV, a non-opioid post-operative pain treatment.
The Company’s development strategy primarily focuses on the FDA’s 505(b)2 regulatory pathway, which is specifically designed for pharmaceuticals for which safety and efficacy of the molecule have already been established. This pathway can reduce the clinical burden required to bring a product to market, and significantly shorten the development timelines and reduce costs and risks.
Hyloris is based in Liège, Belgium. For more information, visit www.hyloris.com and follow-us on LinkedIn.
Our values
Our talented staff work in accordance with our company values:
- We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantages.
- We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
- We believe that the success of the company lies in the competence, dedication, and motivation of each of our employees.
- We believe that freedom returns flexibility and empowerment returns commitment.
Motivation letter and CV can be sent to peter.mertens@hyloris.com
Download a PDF version here
IP Paralegal (part-time)
Location: Anywhere
We are currently looking for a highly organized and detail-oriented IP Paralegal. The successful candidate will play a crucial part in supporting our IP team to protect our IP and set up new patent applications. You are available for 2 days/week.
Job description
As a highly organized and detail-oriented IP Paralegal, you play a crucial part in supporting all the efforts we put into protection of our intelectual property and patents. You are in direct contact with and report into our IP-director, to help prepare legal documents and draft patent applications. You will assist our IP-team to ensure legal compliance and safeguard our ideas and products by helping in the drafting and filing of patent applications. You will also support patent litigations by organizing all documents for legal proceedings.
This means that you will be handling:
- the IP administration in our document management system (IP administration – revising and filing of patent and trademark documents – extracting due dates – docketing due dates – archiving reporting documents – validations – translations – recordals …).
- the preparation, prosecution, and filing of patent applications globally.
- priority documents, power of attorney forms, inventorship declarations.
- communicating with internal business associates and outside counsel regarding patent matters.
- generating reports on portfolio overviews and status reports for IP attorneys and internal business managers.
- administration of requests for IP subsidies.
- invoices from external IP agents, Renewal fees.
You will also be liaising with external IP agents and partners worldwide, as well as with our own R&D and BD team, to support and build up a professional network.
Besides assisting our IP team, you may be supporting our legal team with administrative tasks.
Your professional profile
- You have a background in Science (chemistry, pharma, biology, biochemistry…) or a professional Bachelor in Business Management, Law or similar
- You have a previous experience in intellectual property, preferably within the pharmaceutical or life sciences sector as a patent paralegal – certification is a plus.
- You have a keen interest in Intellectual Property (especially patent protection) and affinity for legal proceedings and its rules and deadlines
- You are interested in admin tasks related to legal and IP in different jurisdictions
- Language skills: fluent in English – spoken and written and one of the official languages of Belgium (Dutch, French, German)
- Computer skills: Microsoft Office (Word, Excel, PowerPoint, Teams) Document Management System – Equinox or similar
Your abilities
- An eye for detail and working in a structured way, together with the flexibility to work in a continuously changing start-up environment
- Hands-on in a growing environment.
- Be proactive and result-oriented with a focus on business.
- You enjoy investigating and digging deeper to find answers/solutions
- High ethical standards with demonstrated experience handling highly sensitive information
- Have affinity for legal proceedings and its rules and deadlines
- Liase and build internal and external contacts.
- Show respect for individuals and cultural difference across different countries.
- A strong and flexible team player attitude
About Our Company
Hyloris is a specialty biopharma company focused on innovating, reinventing, and optimising existing medications to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors. Hyloris has built a broad, patented portfolio of 13 reformulated and repurposed value-added medicines that have the potential to offer significant advantages over available alternatives. Two products are currently in initial phases of commercialisation with partners: Sotalol IV for the treatment of atrial fibrillation, and Maxigesic® IV, a non-opioid post-operative pain treatment. The Company’s development strategy primarily focuses on the FDA’s 505(b)2 regulatory pathway, which is specifically designed for pharmaceuticals for which safety and efficacy of the molecule have already been established. This pathway can reduce the clinical burden required to bring a product to market, and significantly shorten the development timelines and reduce costs and risks. Hyloris is based in Liège, Belgium. For more information, visit www.hyloris.com and follow-us on LinkedIn.
Our values
Our talented staff work in accordance with our company values:
- We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantages.
- We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
- We believe that the success of the company lies in the competence, dedication, and motivation of each of our employees.
- We believe that freedom returns flexibility and empowerment returns commitment.
Motivation letter and CV can be sent to peter.mertens@hyloris.com
Download a PDF version here.
IP Manager
Location: Anywhere
We are currently looking for an IP Manager. The successful candidate will be responsible for overseeing a diverse portfolio of intellectual property rights, from disclosure to protection, which requires constant follow-up.
Job description
As an IP manager:
- You are responsible for managing and maintaining appropriate intellectual property protection of the company’s existing patent) portfolio, including applications, for a wide range of products, under the supervision of the IP Director;
- You assist in overseeing a diverse portfolio of intellectual property rights, from disclosure to protection;
- You follow up patent prosecution, respond to office actions and instruct external agencies timely on procedural actions;
- You will be in contact with different departments of the company and participate in brain-storming sessions, harvest inventions, assist with compiling information for invention disclosures and support the drafting and filing of patent applications;
- You will review new invention disclosures and provide assessment regarding patentability and write – or assist in writing – new patent applications;
- You will organize and carry out patent searches, patent landscapes and FTO’s;
- You will liaise with patent attorneys and with service providers;
- You will help to develop strong intellectual property positions that support commercialization.
Your professional profile
- Master Degree in Pharmacy, Chemistry, Biological Sciences or similar.
- European Patent Attorney or having the desire to become one.
- Experience with research (e.g. during a PhD) and innovation management is a plus.
- Keen interest in intellectual property, especially patent protection and prosecution strategy in the life science area.
- Effective verbal and written communication skills (very good English – written and spoken, French and/or other languages are an asset).
- Computer skills: Microsoft Office (Word, Excel, PowerPoint, Teams) and experience with an IP document management system.
Your abilities
- Flexibility to work in a continuously changing start-up environment.
- High ethical standards with demonstrated experience handling highly sensitive information.
- Have a strong team player attitude with the ability to motivate and to inject energy into the project teams.
- People-centric professional with excellent attention to detail and capable of working in a structured way.
- Have strong interpersonal skills and a collaborative and trust enabling working style for building partnerships among key stakeholders.
- Have the adaptability, flexibility, independence and resourcefulness to roll-up-sleeves and multi-task to thrive in a growing environment.
- Enjoy investigating and digging deeper to find answers/solutions.
- Have affinity for legal proceedings and its rules and deadlines.
- Show respect for individuals and cultural difference across different countries.
- Demonstrate efficient utilization of time and resources.
- Be proactive and result-oriented with a focus on business.
About Our Company
Hyloris is a specialty biopharma company focused on innovating, reinventing, and optimising existing medications to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors. Hyloris has built a broad, patented portfolio of 16 reformulated and repurposed value-added medicines that have the potential to offer significant advantages over available alternatives. Two products are currently in initial phases of commercialisation with partners: Sotalol IV for the treatment of atrial fibrillation, and Maxigesic® IV, a non-opioid post-operative pain treatment. The Company’s development strategy primarily focuses on the FDA’s 505(b)2 regulatory pathway, which is specifically designed for pharmaceuticals for which safety and efficacy of the molecule have already been established. This pathway can reduce the clinical burden required to bring a product to market, and significantly shorten the development timelines and reduce costs and risks. Hyloris is based in Liège, Belgium. For more information, visit www.hyloris.com and follow-us on LinkedIn.
Our values
Our talented staff work in accordance with our company values:
- We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantages.
- We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
- We believe that the success of the company lies in the competence, dedication, and motivation of each of our employees.
- We believe that freedom returns flexibility and empowerment returns commitment.
Motivation letter and CV can be sent to peter.mertens@hyloris.com
Download a PDF version here.
Project Manager
Location: Anywhere
We are currently looking for a Project Manager. The successful candidate will be responsible for managing, coordinating, and delivering product development programs from an early-stage development phase until filing to Health Authorities, launch and routine commercial manufacturing.
Job description
In a matrix organization, as Project Manager, you will:
- Work together with project team members and research scientists who would take on all scientific and technical matters in experimental study designs.
- Prepare target product profiles, project development plans and budgets.
- Prepare and keep up-to-date project timelines and costs and provide input for financial planning.
- Organize efficient external and internal communication (periodic calls, ad-hoc calls, check lists, work specifications).
- Co-ordinate external and internal project responsibilities against objectives and within budget.
- Act as an internal or external point of contact with awareness of technical milestones and timelines as well as contractual obligations.
- Assist with the preparation of requests for proposals and project proposals.
- Monitor progress of individual projects, anticipate and manage risks and use or develop appropriate metrics as required.
- Prepare stage-gate reports for e.g. project strategy, progress, issues, risks, updated timelines and costs.
Your professional profile
- Minimum Qualification: MSc or PhD in Pharmacy, Chemistry or equivalent.
- Minimum Experience: 7 years’ experience in pharmaceutical product development and project management.
- Languages: English (written and verbal) – French is an asset.
- Experienced Microsoft Project software user.
- Ability to understand commercial contracts.
Your abilities
- Demonstrate strong work ethics, and effective written and verbal communication skills.
- Show an organizational aptitude to be part of an outstanding team.
- Be flexible and have a strong team player attitude with the ability to motivate and to inject energy into the project teams.
- Have strong interpersonal skills and a collaborative and trust enabling working style for building partnerships among key stakeholders.
- Have the adaptability, flexibility, independence and resourcefulness to both lead a big vision strategy while also willing to roll-up-sleeves and multi-task to thrive in a growing environment.
- Show respect for individuals and cultural difference across different countries.
- Demonstrate efficient utilization of time and resources.
- Be proactive and result-oriented with a focus on business.
- Can steer external partners.
About Our Company
Hyloris is a specialty biopharma company focused on innovating, reinventing, and optimising existing medications to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors. Hyloris has built a broad, patented portfolio of 16 reformulated and repurposed value-added medicines that have the potential to offer significant advantages over available alternatives. Outside of its core strategic focus, the Company also has 3 high barrier generic products in development and registration phase. Two products are currently in initial phases of commercialisation with partners: Sotalol IV for the treatment of atrial fibrillation, and Maxigesic® IV, a non-opioid post-operative pain treatment. The Company’s development strategy primarily focuses on the FDA’s 505(b)2 regulatory pathway, which is specifically designed for pharmaceuticals for which safety and efficacy of the molecule have already been established. This pathway can reduce the clinical burden required to bring a product to market, and significantly shorten the development timelines and reduce costs and risks. Hyloris is based in Liège, Belgium. For more information, visit www.hyloris.com and follow-us on LinkedIn.
Our values
Our talented staff work in accordance with our company values:
- We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantage.
- We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
- We believe that the success of the company lies in the competence, dedication, and motivation of each of our employees.
- We believe that freedom returns flexibility and empowerment returns commitment.
Motivation letter and CV can be sent to peter.mertens@hyloris.com
Download a PDF version here
Senior Accountant
Location: Liege, Belgium
We are currently looking for a Senior Accountant with a strong background in a production environment. The successful candidate will oversee and manage the financial operations within our group, ensuring accurate and timely financial reporting, analysis, and compliance.
Job description
As a highly organized and detail-oriented Senior Accountant, you are responsible for the finance related activities with the group. You report to our CFO and are in direct contact with internal and external customers, suppliers and auditors. You will be responsible for the daily activities in accounts Payable and Receivable, the monthly closing and you will support in the annual report. You will assist our People Management department in the monthly payroll.
This means that you will be responsible for:
- Accounts Payable: processing purchase invoices + payment batches
- Accounts Receivable: processing sales invoices
- General Ledger: GL entries
- Closing: booking accruals and closing entries
- Preparing the statutory Annual Accounts of 4 companies
- Tax: VAT return, CIT return, R&D Tax credit, Innovative Income deduction
- Payroll: managing the payroll in collaboration with a payroll service provider
- Belspo return: administration and timesheet management
- Assisting the external auditors in the audit process
Your professional profile
- You have a Bachelor’s or master’s in accounting, finance, or a related field
- You have at least five years of relevant experience, preferably in a pharmaceutical or life sciences sector or in a production or manufacturing environment.
- Strong knowledge of generally accepted accounting principles (BE GAAP) and cost accounting principles, as well as VAT and Tax.
- Language skills: French and English, Dutch is a plus (both verbal and written)
- Computer skills: Microsoft Office (Word, Excel, PowerPoint, Teams) – Experience with Business Central is a plus
- Interested in improving the ERP system (Business Central)
Your abilities
- Flexibility and willingness to handle ad hoc tasks and projects as they arise, showcasing adaptability and problem-solving skills.
- A hands-on and pro-active attitude, and you like to get things done
- Like working in an entrepreneurial environment with room to operate and have the appropriate mindset.
- An eye for detail and working in a structured way, together with the flexibility to work in a continuously changing start-up environment
- Enjoy investigating and digging deeper to find answers/solutions
- High ethical standards with demonstrated experience handling highly sensitive information
- Liase and build internal and external contacts.
- Show respect for individuals and cultural difference across different countries.
- A strong and flexible team player attitude
About Our Company
Hyloris is a specialty biopharma company focused on innovating, reinventing, and optimising existing medications to address important healthcare needs and deliver relevant improvements for patients, healthcare professionals and payors.
Hyloris has built a broad, patented portfolio of reformulated and repurposed value-added medicines that have the potential to offer significant advantages over available alternatives. Two products are currently in initial phases of commercialisation with partners: Sotalol IV for the treatment of atrial fibrillation, and Maxigesic® IV, a non-opioid post-operative pain treatment.
The Company’s development strategy primarily focuses on the FDA’s 505(b)2 regulatory pathway, which is specifically designed for pharmaceuticals for which safety and efficacy of the molecule have already been established. This pathway can reduce the clinical burden required to bring a product to market, and significantly shorten the development timelines and reduce costs and risks.
Hyloris is based in Liège, Belgium. For more information, visit www.hyloris.com and follow-us on LinkedIn.
Our values
Our talented staff work in accordance with our company values:
- We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantages.
- We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
- We believe that the success of the company lies in the competence, dedication, and motivation of each of our employees.
- We believe that freedom returns flexibility and empowerment returns commitment.
Motivation letter and CV can be sent to peter.mertens@hyloris.com
Download a PDF version here