We are currently looking for a Scientist Analytical Chemistry. The successful candidate will perform pharmaceutical laboratory operations in an entrepreneurial 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 ethics, 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.

For more information about our company, please visit www.hyloris.com. Motivation letter and CV can be sent to peter.mertens@hyloris.com

We are currently looking for a VP Project Management. The successful candidate will perform lead our experienced PM team.

Job description
As a VP Project Management your role and responsibilities will be to:

• Acts as the strategic and operational driver of the company’s global project portfolio as a key-member of Hyloris’ leadership team.
• Ensures all R&D, clinical, regulatory, quality, IP and commercial development aspects within projects are executed to meet defined timelines, budgets, and targeted value.
• Acts as Senior Point of Contact for service providers, development partners, license holder.
• Organizes internal and external omni-channel communication to co-ordinate project progress.
• Serves as a strong strategic partner to the COO and Hyloris’ Executive Team, providing leadership on project prioritization, execution excellence and long-term portfolio value creation.
• Is a member of key decision-making bodies, including the Project Review Board.
• Provides governance, leadership, and oversight across all development projects, from early feasibility to registration, launch and lifecycle management.
• Ensures cross-functional alignment between Project Management, R&D, Clinical Affairs, Quality & Regulatory, Business Development, Supply Chain and IP.
• Organizes resolution of discontinuities in programs and projects.
• Builds and maintains high-performing PM-team.

Main Tasks
Project & Portfolio Leadership
• Lead global project portfolio, ensuring consistent execution according to defined scopes, deliverables, budgets and timelines.
• Define, develop and implement the overall project governance structure, including KPIs, reporting cadence and escalation processes.
• Evaluate new project proposals (diligence, feasibility, value assessment, risk analysis).
• Provide influential recommendations on TPPs, lifecycle management, business cases, new indications, patent options and strategic priorities.
• Optimize short- and long-term value creation across the portfolio.

Program Execution & Cross-functional Coordination
• Guide PM-team in defining technical programs, development plans and resource needs.
• Ensure seamless day-to-day project follow-up, internal coordination and cross-functional alignment.
• Ensure efficient internal and external communication to secure credibility and leadership towards development partners.
• Coordinate commercial, development, regulatory, quality and technical operations.
• Oversee proactive risk management, including mitigation plans, issue escalation and timeline/cost impact analysis.
• Lead the selection and management of strategic partners.
• Ensure clarity of roles, responsibilities, expectations and contractually defined deliverables.
• Provide oversight on execution to ensure compliance, quality and strategic alignment.

Portfolio Governance & Executive Reporting
• Consolidate accurate internal information and performance dashboards for Executive Team and Project Review Board reporting.
• Flag deviations and propose corrective actions.
• Partner with Business Development, R&D, Clinical Affairs, Regulatory/Quality, IP and Supply Chain to ensure strategic consistency.

Position Requirements

• Minimum Qualifications: M.Sc. / PhD in Pharmacy, Chemistry, Life Sciences, Biomedical Sciences or related field.
• Minimum Experience: Minimum 15 years of experience in drug development, R&D program management and cross-functional project leadership. A minimum of 5+ years leading complex global development programs. Demonstrated experience with portfolio management, external partner management, and regulatory/clinical interfaces.
• Languages: English (written and verbal) required. French or Dutch is an asset.
• Extra: Computer proficiency is mandatory. (PM software)

Abilities

• Strong leadership skills with the ability to motivate, guide and grow high-performing project teams.
• Outstanding written and verbal communication skills.
• Strong strategic thinking, problem-solving skills with an aptitude for providing solutions and business orientation.
• Ability to steer external partners and build collaborative partnerships.
• High adaptability, flexibility, independence and resourcefulness.
• Ability to manage multiple complex programs simultaneously.
• Demonstrated utilization of time and resources efficiently.
• Strong interpersonal skills with respect for multicultural environments.
• Ability to balance strategic “big picture” thinking with hands-on operational execution.
• Ethical, proactive, assertive, and results-oriented mindset.
• Adaptability, flexibility, independence, and resourcefulness to both lead a big vision strategy while also being willing to roll-up-sleeves and multi-task to thrive in a start-up environment dedicated to growth.

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.

For more information about our company, please visit www.hyloris.com. Motivation letter and CV can be sent to peter.mertens@hyloris.com

Role & Responsibilities
Support the Finance team in day-to-day accounting operations under BE GAAP, ensuring accuracy and compliance. Assist in financial reporting and contribute to maintaining efficient accounting processes.

Main Tasks
• Accounts Payable: Assist in processing purchase invoices + payment batches
• Accounts Receivable: Support in processing sales invoices and follow-up on outstanding payments.
• Post basic GL entries under supervision.
• Help with accrual bookings and closing entries.
• Learn and support administration tasks; act as a junior key user.
• Assist with VAT returns and other tax-related filings.
• Support of Sen. Accountant in the audit process with external auditors

Postition Requirements
• Minimum Qualification : Bachelor’s in accounting, finance, or a related field
• Minimum Experience: You have max 2 years of relevant experience (internship or entry-level role preferred – pharma or international experience is a plus
• Languages: English (written and verbal) and French, Dutch is an asset.

Abilities
• Strong attention to detail and willingness to learn.
• Good organizational skills and ability to work in a team.
• Adaptability, flexibility, independence, and resourcefulness to roll-up-sleeves and multi-task to thrive in a growing environment.
• Respect and understanding for cultural differences in different countries, and efficient utilization of time and resources.
• Knowledge of Generally Accepted Accounting Principles (BE GAAP) and cost accounting principles, as well as VAT and Tax.
• Experience with Business Central is a plus
• You have a hands-on and pro-active attitude, and you like to get things done
• You like working in an entrepreneurial and dynamic environment with room to operate, have the appropriate mindset and are hands-on and flexible

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.

For more information about our company, please visit www.hyloris.com. Motivation letter and CV can be sent to peter.mertens@hyloris.com