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Senior Project Manager - Medical Device - Liège

Founded in 2016, Oncoradiomics is an innovative and ambitious start-up based in Liège. Oncoradiomics‘s strategic goal is to “revolutionize precision medicine”, by applying advanced artificial intelligence to clinical imaging.

Oncoradiomics focuses on tailoring cancer care to the clinical, imaging, biological and genetic characteristics of an individual patient so that the best outcome can be achieved.

Oncoradiomics holds several international grants and patents and is continuously developing and connecting with leading industrial and academic players to advance healthcare and the life sciences.

For the expansion of the team in Liège and in order to manage key clients’ and internal R&D projects, we are looking for a (m/f):

Senior Project Manager

Responsibilities:

As a Senior Project Manager, you are responsible for the delivery of the projects. You coordinate people and processes to ensure that key customers’ projects are delivered on time and achieve the desired results. Regarding the R&D projects, you lead the team in order to meet strategic objectives and the company’s ambition.

Reporting to the CEO, you lead the innovation throughout the company. Your main responsibilities are:

  • You monitor multiple projects from initiation through delivery and ensure that all projects are delivered on time, within scope and budget.
  • You identify and clarify key projects requirements and customers’ needs, along with scientists, regulatory, sales and management expectations.
  • You work with key stakeholders and with the CEO to understand requirements, address business and system issues, in order to ensure that strategic goals are met.
  • You maintain schedules, track key milestones and program interdependencies and preempt risks.
  • You resolve conflicts in a timely manner to ensure that projects stay on track.
  • You oversee and manage the operational aspects of ongoing projects and serve as liaison between program management, planning and scientists’ team.
  • You review status of projects and budgets; you report results and work evolution on a regular basis to the top management.
Profile:
  • Bachelor’s or Master’s degree in IT, Engineering, Business, Mathematics or equivalent through experience.
  • Min. 7 years of experience in a project management position with technical products. Experience within a research environment or in medical imaging software and/or devices is a plus.
  • Experience with managing data solution, platform projects and AI technologies.
  • Experience in a Medical device or regulated industry and exposure to regulatory submissions. Understanding of FDA regulations including ISO 13485.
  • Project management methodology and Agile/Scrum Master certification are an asset.
  • Results and customer oriented, rigorous, structured, autonomous and flexible.
  • Analytical, organized, team player, open-minded with a start-up mind-set.
  • Strong transversal leadership and communication skills.
  • Perfect command in spoken and written French and English. Any other language is an asset.
  • Willing to travel for short periods, up to 20% of your time.
Offer:
  • A challenging and diversified position within a high-potential innovative start-up company.
  • To work in a dynamic, respectful and professional
  • International exposure, with learning and development opportunities.
  • An attractive compensation package in line with the position responsibilities and your experience.

Medical Manager - Biotech, Biotechnology - Mont-Saint-Guibert

NOVADIP BIOSCIENCES (www.NOVADIP.com) is an innovative biotech company expert in the development of novel regenerative medicines. This human-sized structure is a leader in new generation therapies for hard & soft tissue reconstruction from autologous adipose stem cells.

NOVADIP BIOSCIENCES shows the ambition to grow to a worldwide class, with a successful closing of a 28M€ fund raising. Its main objective for the coming years is to develop its portfolio of products and to perform clinical validation and process industrialization of its main compounds.

NOVADIP BIOSCIENCES is a French/English-speaking work environment based in Mont-Saint-Guibert (close to University of Louvain-la-Neuve and Brussels area), Belgium, Europe.

In order to support our clinical development in the USA, we are actively looking for a (m/f):

Medical Manager

Responsibilities:

As a Medical Manager, you are part of the Medical Department consisting of the Chief Medical Officer, a Compliance Manager, 2 Clinical Project Managers, 2 Clinical Research Associates and a Clinical Research Assistant. You closely collaborate with them.

Your main responsibilities are as follows:

  • Design, contribute and write new study protocols and documentation related to clinical trials (IMPD/IND, investigator brochure, sponsor master files, patient informed consent, CRF, monitoring plan, safety plan /DSMB…) and contribute to the design of clinical development plans.
  • Develop and maintain a network of medical experts in the field and work in close collaboration with internal departments (i.e. R&D, Regulatory Affairs, Manufacturing, logistics…).
  • Identify, screen, select, and initiate contacts with clinical sites, CROs, and other sub-contractors in the USA for the future trials in collaboration with clinical team.
  • Set up pharmacovigilance program (standalone or in collaboration with CRO).
  • Manage the interactions with ethics committees.
  • Monitor trials from a medical point of view, together with internal staff and clinical sites personnel.
  • Review incoming clinical data, and write medical reports or any other scientific files in collaboration with the Chief Medical Officer.
  • Facilitate communication flow between the clinical sites, CROs and Novadip.
  • Share your knowledge with the teams in order to overcome scientific, operational, regulatory, marketing, financial and strategic challenges within the company.
  • Active participation in training/coaching of operational teams involved in clinical trials (internal and external).
  • Report to the Chief Medical Officer.
Profile:
  • MD, PhD in Medical Sciences or Master in sciences or related field.
  • Min. 5 years of experience within either a CRO or a Pharma/Biotech/Medtech company. Experience in cell therapy is a great asset.
  • In depth understanding of processes related to clinical development plans, clinical trials, and superior knowledge of IHC-GCP.
  • Interest in basic sciences and translation of medical science in new clinical trials protocols.
  • Good communication skills with both clinical and non-clinical contacts.
  • Excellent attention to details and established organizational skills.
  • Demonstration of flexibility, professionalism, good interpersonal skills and managerial skills.
  • Fluency in written and spoken English is required. Good level of Dutch or French is a plus.
  • Willingness and ability to be based in USA or to travel frequently to the USA.
  • To be in the possession of a full driving license.
Offer:

A diversified full-time permanent position within a high-potential innovative biotech company.

  • To work in a human-sized, dynamic, respectful and professional environment.
  • The opportunity to take part in a challenging scientific and business growth.
  • Varied contacts inside the company and with the biotech/pharma sector.
  • An attractive salary package in line with the position responsibilities and your experience.

Research Assistant – Flow Cytometry and Serology – Evenings and weekends – - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium), offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical samples.

Caprion operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotechs.

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Research Assistant for its flow cytometry and serology platforms, for its site in Gosselies, Belgium.

Research Assistant – Flow Cytometry and Serology – Evenings and weekends

Function :

Reporting to the Associate Director, Operations and working closely with Principal Scientists, the Research Assistant will work within a team focusing on the characterization of the cellular (ELISPOT and various flow cytometry assays such as phenotyping of PBMC, detection of intra-cellular cytokines, etc) and of the humoral (ELISA, Luminex, viral neutralization tests, etc) immune response. You will receive a strong training to further develop your skills in cellular and humoral immunology.

Tasks include :

  • Perform immunoassays according to current standard operating procedures;
  • Participate to the writing and/or to the review of method SOP and worksheets;
  • Manage reagents inventories and orders;
  • Participate to the technical management of the laboratory;
  • Perform work according to internal quality standards, apply relevant Quality System procedures and participate to the continuous improvement of Quality documents;
  • Attend relevant internal training activities;
Profile of the applicant :

The applicant must hold a bachelor degree or a master’s degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology.  Practical knowledge of techniques related to cellular and humoral immunology is required.  Experience in cell culture and handling infectious materials in BL2+ environment is an asset.

The applicant must :

  • Demonstrate excellent organisational skills.
  • Demonstrate schedule adaptability and flexibility.
  • Must be able to work evenings and weekend hours.
  • Be willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
  • Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation procedures (GDP).
  • Be functional in French (spoken and written) and have a functional knowledge of written English. Knowledge of spoken English is an asset.
Offer :
  • Full time permanent contract, with possibility of rapid start.
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Strong training and development opportunities.
  • A competitive salary package including benefits (and premium for evenings and weekend hours), adapted to your experience and the context.

Medical Director - Biotechnology - Gosselies

Minoryx (www.minoryx.com) is a clinical stage biotech company leading the development of new therapies for rare diseases affecting the central nervous system. The company is backed by strong international investors.

The company’s leading program is currently in an ongoing phase II/III clinical trial in EU and US, with results expected in 2020. In the upcoming months, Minoryx is planning to launch a clinical trial for a second orphan indication.

Founded in Spain, Minoryx is opening a subsidiary in Gosselies (Belgium). In order to strengthen the team in Belgium, we are currently looking for a (m/f):

Medical Director

Responsibilities:

As a Medical Director, you provide scientific support to the company as a whole and particularly to planned ongoing clinical research activities. You collaborate with an internal multidisciplinary team to successfully execute the company’s development program strategies and operations.

Your main responsibilities are:

  • Provide medical expertise for project and study development.
  • Write clinical trial materials, including trial synopsis and protocol.
  • Monitor ongoing clinical studies for protocol adherence and safety.
  • Contribute to and review documentation related to clinical trials (e.g. investigators brochures).
  • Review clinical study reports designed by third parties.
  • Screen information from journal publications and conference presentations for relevant developments in the company’s indications.
  • Develop and maintain broad and deep relationships with external partners.
Profile:
  • MD, ideally in neurology or in neurosciences.
  • At least 5 years of relevant working experience in the pharmaceutical Industry, in hospitals or in biotech companies.
  • Extensive knowledge of all aspects of GCP and regulations.
  • Experience in clinical research in orphan indications or with brain imaging technologies is an asset.
  • Strong collaboration, documentation and presentation skills.
  • Flexibility, good time management, team-working skills, stress resistant, and ability to work proactively and independently.
  • Well-developed communication skills, problem solving skills, creative and critical thinking.
  • Fluent in English. A good command of French and/or Catalan is an asset.
  • Prepared to travel to the Spanish site regularly, clinical investigational sites, conferences and meeting with regulators.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience

Research Assistant – Flow Cytometry and Serology - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences is a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium). Caprion Biosciences offers analytical services to biopharmaceutical companies ranging from mass spectrometry-based analytical services to the characterization of the human immune response in clinical samples.

Caprion Biosciences operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotech companies.

In the context of its growing immune monitoring service offering in Gosselies (Belgium), we are looking for a (m/f):

Research Assistant – Flow Cytometry and Serology

Responsibilities :

Reporting to the Laboratory Manager and working closely with Principal Scientists, the Research Assistant will work within a team focusing on the characterization of the cellular (ELISPOT and various flow cytometry assays such as phenotyping of PBMC, detection of intra-cellular cytokines, etc) and of the humoral (ELISA, Luminex, viral neutralization tests, etc) immune response.

Tasks include :

  • Perform immunoassays according to current standard operating procedures;
  • Participate to the writing and/or to the review of method SOP and worksheets;
  • Manage reagents inventories and orders;
  • Participate to the technical management of the laboratory;
  • Perform work according to internal quality standards, apply relevant Quality System procedures and participate to the continuous improvement of Quality documents;
  • Attend relevant internal training activities;
  • Depending on the experience level of the candidate, additional tasks may include:
    • Act as a leader in the laboratory for specific studies;
    • Work with the Principal Scientist to prepare experimental plans needed for the conduct of immune monitoring assays;
    • Participate in the development and qualification/validation of complex methods;
    • Participate in experiment planning and problem solving.
Profile :

The applicant must hold a bachelor degree or a master’s degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology and demonstrate a relevant laboratory experience. Theoretical and practical knowledge of techniques related to cellular and humoral immunology is required. Experience in cell culture and handling infectious materials in BL2+ environment is an asset.

The applicant must :

  • Demonstrate excellent organisational skills.
  • Demonstrate schedule adaptability and flexibility.
  • Be willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
  • Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation procedures (GDP).
  • Be functional in French (spoken and written) and have a functional knowledge of written English. Knowledge spoken English is an asset.
Offer :
  • Full time permanent contract, with possibility of rapid start.
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Training and development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.

Principal Scientist - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada) and Gosselies (Belgium), offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical samples.

Caprion operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotechs.

For its site in Gosselies and in the context of its growing immune monitoring service offering, Caprion is looking for a (m/f) :

Principal Scientist

Responsibilities :

Reporting to the Director of Scientific Operations and working closely with the laboratory personnel, the Principal Scientist will work within a team focusing on the characterization of the cellular and humoral immune response, using various types of assays such as flow cytometry (phenotypic, ICS, etc) ELISPOT, ELISA, Luminex and viral neutralization tests.

Responsibilities include:

  • Overseeing experimental design of flow cytometry, ELISPOT and antibody-based assays through generation of study-specific workplans and supporting documentation
  • Acting as a key resource to provide guidance and support in root cause analysis and impact assessment
  • Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress
  • Data interpretation, report generation and presentation of results to clients
Profile :

The applicant must hold a doctorate degree in life science, with strong knowledge of immunology, with post-doctoral experience (or equivalent) and have a deep expertise of flow cytometry analysis. The applicant must also have a minimum of two years of experience in the industry.

The applicant must :

  • Be proficient with analysis software such as FlowJo, Pestle, Spice, Prism and Excel and be able to perform complex analysis of flow cytometry data such as Boolean analysis.
  • Demonstrate excellent communication and organisational skills.
  • Be abreast of latest immune monitoring methodologies
  • Have an excellent knowledge and understanding of GCLP regulations and other regulatory guidelines sufficient to carry out GCLP studies.
  • Be willing to work in a Quality environment (ISO17025, GCLP, GMP) and apply good documentation practices (GDP).
  • Be fluent in English (written & spoken) and able to functionally communicate in French.
Offer :
  • Full time permanent contract.
  • Diversified tasks and responsibilities and interesting projects.
  • A professional, dynamic and stimulating work environment.
  • Development opportunities.
  • A competitive salary package including benefits, adapted to your experience and the context.

Clinical Trial Manager - Biotechnology - Gosselies

Minoryx (www.minoryx.com/) is a clinical stage biotech company leading the development of new therapies for rare diseases affecting the central nervous system. The company is backed by strong international investors.

The company’s leading program is currently in an ongoing phase II/III clinical trial in EU and US, with results expected in 2020. In the upcoming months, Minoryx is planning to launch a clinical trial for a second orphan indication.

Founded in Spain, Minoryx is opening a subsidiary in Gosselies (Belgium). In order to strengthen the team in Belgium, we are currently looking for a (m/f):

Clinical Trial Manager

Responsibilities:

Reporting directly to the Director of Clinical Operations and working closely with the team in Spain, you are responsible for the operational management and the oversight of clinical trials according to the clinical strategy.

Your main responsibilities are:

  • Coordinate clinical trial in collaboration with selected CRO.
  • Visit clinical study sites regularly and interact with study members.
  • Ensure successful execution of the clinical trials on time and on budget.
  • Review study related documentation and materials.
  • Co-monitor clinical study for protocol adherence and safety with selected CRO.
  • Ensure that clinical trial activities are documented in accordance with regulatory requirement.
  • Create and maintain effective relationships with KOL.
  • Report results and work evolution on a regular basis to the Director of Clinical Operations.
Profile:
  • Master’s or bachelor’s degree in Life Science or equivalent through experience.
  • At least 5 years of relevant experience in clinical trials.
  • Extensive knowledge of all aspects of GCP and regulations.
  • Track record on managing clinical studies on time & on budget.
  • Good collaboration, documentation and presentation skills.
  • Flexibility, good time management, team-working skills, stress resistant, ability to work proactively and independently.
  • Well-developed communication skills, problem solving skills, creative and critical thinking.
  • Excellent command of Microsoft Office Tools (Excel, Word, PowerPoint).
  • Fluent in English. A good command of French or Catalan is an asset.
  • Prepared to travel to Spanish site regularly, clinical investigational sites, conferences and meeting with regulators.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience.

Interested ?

Pharmacien d’Industrie (QP) - Bio-Pharma/Biotech - Woluwé-Saint-Lambert

Située à Woluwe-Saint-Lambert, ß+ Pharma est une société spécialisée dans la production de radio-isotopes innovants à usage médical et destinés au diagnostic de maladies oncologiques, cardiologiques et neurologiques. Sa production couvre les besoins de ses clients sur le territoire du BeNeLux et une partie de la France.

Fondée en 2002 et composée de 11 collaborateurs, ß+ Pharma offre un environnement dynamique et un réel esprit d’équipe permettant l’épanouissement de tous ses employés.

ß+ Pharma fait partie du groupe Curium Pharma.

Afin de contribuer au développement de ß+ Pharma, nous sommes activement à la recherche d’un (h/f):

Pharmacien d’Industrie (QP)

Responsabilités:

En tant que Personne Qualifiée Adjointe, vous supervisez la production des radio-pharmaceutiques dans le respect des normes GMP et vous assurez la libération des lots. Vous rapportez directement à la Personne Qualifié Principale.

Vos principales tâches sont :

  • Libérer les lots produits en veillant à respecter les délais et les normes de qualité.
  • Participer aux activités de fabrication des radio-pharmaceutiques.
  • Gérer le système de qualité en accord avec les normes GMP.
  • Assurer le bon fonctionnement des activités de maintenance, de qualification, de validation et d’approvisionnement du service.
  • Participer à la formation initiale et continue du personnel.
  • Participer aux audits fournisseurs ainsi qu’aux audits sur les autres sites de production européens.
Profil:
  • Vous disposez d’un Master en Pharmacie, d’un Master complémentaire en Pharmacie Industrielle ainsi que d’un numéro QP.
  • Vous possédez une expérience avérée dans le domaine en industrie (radio-/bio-) pharmaceutique. Les candidatures sortant fraichement des études sont également les bienvenues.
  • Vous êtes respectueux(se), digne de confiance et aimez le travail en équipe.
  • Vous êtes flexible et faites preuve de rigueur.
  • Vous êtes dynamique et proactif(ve) et disposez de bonnes capacités de communication.
  • Vous maitrisez l’anglais et le français à l’oral comme à l’écrit.
Offre:
  • Une fonction diversifiée au sein d’une société en développement.
  • L’opportunité de rejoindre un environnement à taille humaine, dynamique et professionnel.
  • Un parcours de formation dès l’entrée en fonction et tout au long de votre évolution.
  • Un contrat à durée indéterminé assorti d’un package salarial attractif.

Head of Regulatory Affairs – Gosselies - Biotechnology - Gosselies

Minoryx is a clinical stage biotech company leading the development of new therapies for rare diseases affecting the central nervous system with a high unmet medical need. The company is backed by strong international investors.

Minoryx’s leading program is currently in an ongoing phase II/III clinical trial in EU and US, with results expected in 2020. In the upcoming months, the company is planning to launch a clinical trial for a second orphan indication. Please visit http://www.minoryx.com/.

Founded in Spain, Minoryx is opening a subsidiary in Gosselies (Belgium). In order to strengthen the team in Belgium, we are currently looking for a (m/f):

Head of Regulatory Affairs

Responsibilities:

As a Head of Regulatory Affairs, you serve as a key and active member of the director leadership team, making sure regulatory objectives are met. You lead the organization on regulatory affairs, coordinate with regulatory advisors and mentors and provide training and interpretation of global regulatory requirements to all company personnel.

Your main responsibilities are:

  • Provide regulatory strategy and lead all regulatory interactions.
  • Author or co-author all regulatory documents (background documents, orphan designations, other) with appropriate support as needed.
  • Serve as liaison with EMA/CHMP.
  • Coordinate all FDA interactions with the support of US personnel (contractor or internal).
Profile:
  • Master’s degree in life sciences or equivalent through experience.
  • 10 years of experience in regulatory affairs within pharma/biotech industry.
  • Experience with both FDA & EMA.
  • Experience on processes such as ODD, fast track designation, PRIME, breakthrough and/or pediatric review priority voucher.
  • Experience in small molecules and orphan drugs is an asset.
  • Flexible, good time management, team-working skills, stress resistant, ability to work proactively and independently.
  • Well-developed communication skills, problem solving skills, creative thinking.
  • Fluent in English. A good command of French and/or Catalan is an asset.
  • Prepared to travel to Spanish site regularly.
Offer:
  • An interesting position within a high-potential clinical stage biotech company.
  • The opportunity to work in a human-sized and multicultural team environment.
  • A variety of interesting contacts with international exposure.
  • An attractive salary package in line with the position responsibilities and your experience.

 

Laboratory Coordinator - Bio-Pharma/Biotech - Gosselies

Caprion Biosciences, a contract research organisation with facilities in Montreal (Canada), Gosselies (Belgium) and Freemont (USA), offers analytical services to biopharmaceutical companies for the characterization of the human immune response in pre-clinical and clinical samples.

Caprion operates globally, with partners in North America, Europe and Asia, including large pharmaceutical companies and biotechs.

In the context of its growing immune monitoring service offering, Caprion is looking to hire a Laboratory Coordinator, for its site in Gosselies, Belgium.

Laboratory Coordinator

Function :

Reporting to the Associate Director, Operations, the Laboratory Coordinator is responsible for the instrument logistics, biosafety, monitoring of instruments and facilities and overall management of laboratory area.

Tasks include :

  • Scheduling and overseeing external maintenance and calibration of all instruments and equipments;
  • Performing internal qualification of basic equipments (i.e. pipette calibration, balance calibration, thermal mapping of storage equipments);
  • Ensuring that equipments are used, maintained and calibrated as per SOP;
  • Ensuring that equipment log books are complete and properly maintained; ensuring that calibration reports are completed in a timely manner;
  • Managing all instruments and equipment malfunctions and associated documentation as per SOP;
  • Purchasing of new equipments (obtaining quotes, ensuring that IQ/OQ/PQ is performed and documented as per SOP);
  • Management of the monitoring system for facilities and instruments;
  • Ensuring laboratory areas are adequately maintained (planning of maintenance, repair, decontamination and cleaning of laboratory space);
  • Managing Health and Biosafety for the site;
  • Training laboratory personel on laboratory biosafety rules and equipment operations;
  • Participating to the writing and review of laboratory equipment SOP;
  • Ensuring that all above laboratory management activities are documented according to GDP procedures;
  • Participating in client and/or regulatory agencies audits.
Profile of the applicant :

The applicant must hold a bachelor degree (or the equivalent) in a life science discipline such as biology, medical biology or biochemistry/biotechnology.  The applicant must have a minimum of 5 years in a similar position.  Experience in working in a Quality environment is an asset.

The applicant must :

  • Be meticulous, thorough and proactive;
  • Demonstrate excellent organizational skills;
  • Demonstrate schedule adaptability and flexibility.
  • Be willing to actively participate to the generation, the implementation and the continuous improvement of laboratory processes.
  • Be willing to work in a Quality environment (ISO15189, GCLP, GMP) and apply good documentation procedures (GDP).
  • Be functional in French and English (spoken and written).
Offer :
  • Full time permanent contract, with possibility of rapid start.
  • A professional, dynamic and stimulating work environment.
  • A competitive salary package including benefits, adapted to your experience and the context.

Other career opportunities

41 results

Chief Operating Officer - Biotechnology - Brabant wallon

A-MANSIA is a biotech company focusing on microbiome therapeutics addressing human health issues like obesity and related disorders. The mission of A-MANSIA is to provide innovative solutions based on Microbiome Therapeutics.

Under the implementation plan in the Walloon Brabant province, its future development and reinforced by a 21 million euros fundraising success, A-MANSIA is looking for a dynamic and enthusiastic person to strengthen the team. For more information about the company and the technology, please contact us via recruitment@pahrtners.be.

A-MANSIA offers a French, Dutch and English-speaking environment, culturally diversified and located in the heart of Europe, in Belgium, a few hours from European Capitals.

To strengthen the team in Mont-Saint-Guibert, we’re looking for an (m/f):

Chief Operating Officer

Main responsibilities:

Reporting directly to the CEO and as part of the executive committee, you are in charge of the whole operations management for the fermentation process starting from the sourcing of raw materials to the commercialisation of finished products. You are the point of contact with the CMO(s) in charge of the outsourced manufacturing of microbial products.

Your main tasks are:

  • Lead production projects and product launch on the market: sourcing of raw materials with the CMO, logistic, galenic development & packaging.
  • Coordinate with R&D and marketing departments to oversee the whole operation process.
  • Coordinate the whole outsourced production and supply chain.
  • Be part of the COMEX and report to Board of Directors on the strategic development of operations.
  • Define specifications, negotiate contracts and manage the collaboration with CMOs and third parties.
  • Ensure raw materials compliance and control outsourced performances.
  • Control and lead the Cog’s at the product launch and on a long-term basis.
  • Manage the internal supply chain team.
Profile:
  • You hold a Ph.D. or you are engineer in Nutrition or Life Sciences, or equivalent through experience.
  • You have at least 10 years of industrial experience in production management related to the production of probiotics/food complements.
  • You have experience in and knowledge of fermentation processes.
  • You have hands on experience in or knowledge of CMO and third parties management.
  • You show strong leadership skills combined with a strategic and hands-on approach.
  • You are skilled in project management related to food complements launch on the market.
  • You take advantages of an extended network in the industry.
  • You are rigorous, flexible, hands-on, independent, dynamic and pro-active.
  • You are fluent in English. The command of French and/or Dutch is an asset.
Offer :
  • A diversified executive position within a high-potential start-up company.
  • A key position for the development of the company.
  • The opportunity to join a human sized, dynamic and professional environment.
  • A permanent employment contract.
  • An attractive compensation package in line with your experience.

Supply Chain Technician – Warehouse - Bio-Pharma/Biotech - Mont-Saint-Guibert

Promethera Biosciences (www.promethera.com) is a global innovator in liver cell-based medicines whose mission is to help patients overcome acute and chronic liver diseases. Its lead clinical program, derived from their patented cell technology platform HepaStem, is designed to benefit from its immune-modulatory and anti-fibrotic properties.

For all its activities, Promethera is taking a global view early on to pursue a development strategy that maximizes the probability of success.

Promethera currently employs a talented international workforce comprising around 70 talented and diverse people in Belgium, the US and Japan.

To strengthen the team in Mont-Saint-Guibert, we’re actively looking for a (m/f):

Supply Chain Technician – Warehouse

Responsibilities:

Reporting to the Supply Chain Supervisor, you are responsible for typical supply chain operations and logistic functions. Working in pair, you are the backup of other supply chain technician.

Your main responsibilities are:

  • You take delivery of the raw materials and documents.
  • You label and physically store raw materials.
  • You establish the conformity (vs. orders) and integrity of delivered goods.
  • You follow-up with suppliers and obtain from the supplier any information required for release.
  • You ensure the storage room comply with GMP principles and is cleaned according to plan.
  • You ensure the waste areas are tidy. You manage waste removal.
  • You ensure accuracy of the inventory and perform planned inventory counts.
  • You liaise with quality assurance to have the raw material released.
Profile:
  • Bachelor Degree in a related-field, or equivalent through experience.
  • Experience in a logistics position within a pharma/biotech environment.
  • Understanding of relevant regulations (E.G. Incoterms, ADR, GDP, customs, wastes management).
  • Be willing to work in compliance with Good Manufacturing Practices (GMP).
  • Familiar with MS Office Solutions and Warehouse Management Systems.
  • Self-motivated, team player, autonomous, rigorous and flexible to work in multitasks environment.
  • Be fluent in French (written & spoken) and able to functionally communicate in English.

Offer:

  • A diversified full-time permanent position within a high-potential innovative company.
  • To work in a human-sized, dynamic, respectful and professional environment.
  • Varied contacts inside the company and with the pharma sector.
  • An attractive salary package in line with the position responsibilities and your experience.

Program Management Officer - Biotechnology - Gosselies

Located in Gosselies (Belgium), MaSTherCell is a service company (CDMO) in biotechnology. MaSTherCell is specialized in production outsourcing, process development and quality management (QA/QC/QP) for cell therapy.

With around 140 employees, MaSTherCell supports its customers (big pharma, biotech, etc.) in the development and production of innovative medicines. MaSTherCell actively contributes to improving the quality of life and health of many patients. For more information, please visit http://www.masthercell.com.

To support MaSTherCell in its strong growth, we are actively looking for a (m/f):

Program Management Officer
Responsibilities:

Reporting to the Executive committee, you assist them in selecting and planning strategic internal projects/programs (including new sites integration), and in reporting on their progress.

Your main responsibilities are:

  • You implement project management tools, project control processes, procedures and policies.
  • You monitor and control the internal program/project throughout their entire lifecycle.
  • You select program/project and you argue program/project closedown if necessary.
  • You assess the relative priority of internal projects and programs.
  • You set up performance reporting and program/project governance for customer and internal projects.
  • You lead the project financial tracking with the business controller.
  • You provide support to project teams and task planning.
  • You report your work on a regular basis.
 Profile:
  • Master’s degree or equivalent through experience.
  • Minimum 5 years experience in a project management officer position.
  • A project management professional certification is an asset.
  • Strong communication skills together with hands-on and pragmatic mind-set.
  • Very good organizational, analytical and problem-solving skills.
  • Highly collaborative, self-motivated and team-oriented individual in a company setting.
  • Good oral and written communication skills in English. Any other language is a plus.
  • Computer skills:  Microsoft office, Digital document management system and Project management IT tools.
Offer:
  • A challenging and diversified position within a high-potential innovative biotech company.
  • To work in a human size, dynamic, respectful and professional environment.
  • A variety of interesting contacts with international exposure.
  • An attractive compensation package in line with the position responsibilities and your experience.

Network & Security Engineer and Architect - IT & Consultancy Solutions - Louvain-la-Neuve

Fondée en 2015, PROCSIMA-GROUP est une entreprise spécialisée en sécurité informatique. PROCSIMA-GROUP aide les entreprises à protéger leurs informations et leurs données contre les attaques externes et internes de toute nature, et à assurer la bonne performance de leurs systèmes ainsi que la bonne disponibilité de leurs services.

Située à Louvain-la-Neuve et composée d’une quinzaine de consultants, PROCSIMA-GROUP vise à devenir le leader belge de la cyber protection en fournissant des services, de la consultance et des solutions à haute valeur ajoutée, tels que : services d’audit & reviews, protection des données, stratégie, architecture, gouvernance, GDPR, etc.

Pour de plus amples informations, veuillez consulter http://www.procsima-group.eu.

Afin de renforcer l’équipe, nous sommes activement à la recherche (CDI ou freelance) d’un(e) :

Network & Security Engineer and Architect

 Responsabilités :

En tant que Network & Security Engineer and Architect, vos principales responsabilités sont les suivantes :

  • Réaliser des audits et études de robustesse et d’architecture du réseau et de la sécurité mise en place chez les clients, notamment via des tests d’intrusion et de pénétration.
  • Conseiller le client en fournissant des recommandations concrètes.
  • Proposer au client une feuille de route et une stratégie à court, moyen et long terme.
  • Accompagner le client dans ses projets d’amélioration et à la mise en place de la stratégie.
  • Participer à des projets en tant qu’ingénieur spécialisé en réseau et sécurité, et en tant qu’architecte de sécurité.
  • Créer les designs avec méthode et conseiller les équipes projets et opérationnelles.
  • Participer à la gestion et à l’amélioration des services de sécurité des réseaux de PROCSIMA-GROUP.
Profil :
  • Vous disposez idéalement de 3 à 5 ans d’expérience dans une position similaire. Les profils juniors sont également les bienvenus.
  • Vous maitrisez le design des architectures réseau.
  • Vous possédez une bonne connaissance générale des firewalls les plus utilisés (Palo Alto, Checkpoint, Fortinet, F5, etc.) et des proxys, reverse proxys et autres équipements (Bluecoat, etc.).
  • Vous avez des notions de gestion de projet (Prince2 ou PMI), et avez une bonne connaissance des systèmes de gouvernance ITIL et CobiT. Une certification réseau Cisco, Ethical Hacking ou en cybersécurité est un sérieux atout.
  • Vous êtes pragmatique, organisé(e), autonome, et doté(e) d’un bon esprit d’analyse et de synthèse.
  • Vous faites preuve d’un esprit d’équipe développé et avez de bonnes compétences communicationnelles et d’écoute.
  • Vous communiquez aisément en français. La connaissance de l’anglais/néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer en fonction des missions (Bruxelles, Wallonie).
Offre :
  • Intégrer une entreprise en pleine croissance proposant des solutions innovantes et variées.
  • Une fonction challengeante et diversifiée dans un secteur en plein développement.
  • L’opportunité de travailler sur divers projets pour le compte de différents clients.
  • La possibilité de travailler sous contrat à durée indéterminée ou en tant que freelance.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs en phase avec votre expérience.
  • Un plan de formation en adéquation avec des objectifs de développement clairs.

Regulatory Manager - Medical Device - Liège

Founded in 2016, Oncoradiomics is an innovative and ambitious start-up established in Liège. Oncoradiomics‘s strategic goal is to “revolutionize precision medicine”, by applying advanced artificial intelligence to clinical imaging.

Oncoradiomics focuses on tailoring cancer care to the clinical, imaging, biological and genetic characteristics of an individual patient so that the best outcome can be achieved.

Oncoradiomics holds several international grants and patents and is continuously developing and connecting with leading industrial and academic players to advance healthcare and the life sciences.

Regulatory Manager

Responsibilities:

As a Regulatory Manager, you lead and drive the execution of Oncoradiomics global regulatory strategy. Reporting to the CEO, you define and implement the regulatory policy in line with applicable directives, guidelines and legal requirements. Your main responsibilities are:

  • You drive regulatory strategy for EU/US markets: develop global regulatory strategies and drive the international product registration activities (with focus on EU, US, Canada, Australia, Japan, China and South Korea).
  • You prepare, organize, and submit global regulatory submissions/approvals.
  • You prepare and submit regulatory filings including, CE marking, traditional and special 510(k) applications, letters to file, technical files, etc.
  • You ensure regulatory requirements for establishment registrations, device listings, and registration licensing is maintained.
  • You perform MDR and MDV complaint reporting assessments.
  • You support the product development team in the implementation of regulatory requirements, including review of design input, risk management, and test documentation.
  • You perform regulatory assessment of product changes.
  • You proactively interpret regulatory guidelines and regulations, anticipate concerns, educate, and integrate requirements into product development programs.
  • You review and approve marketing materials to ensure compliance with advertising and promotional regulations.
  • You support internal and external audits.
Profile:
  • Master or PhD in life sciences or equivalent through experience.
  • 10 years experience in a RA position in the (software solutions) MedTech sector.
  • Proven track record of building strong relationships with internal and external stakeholders.
  • Ability to maintain multiple projects and meet timelines, including change management skills.
  • Client-centered and solution-oriented, with hands-on and pragmatic mindset.
  • Excellent leadership, communication and interpersonal skills.
  • Fluency in English.
Offer:
  • A challenging and diversified position within a high-potential innovative start-up company.
  • To work in a dynamic, respectful and professional
  • International exposure, with learning and development opportunities.
  • An attractive compensation package in line with the position responsibilities and your experience.

Project Manager Sécurité/Infrastructure/Réseau - IT & Consultancy Solutions - Louvain-la-Neuve

Fondée en 2015, PROCSIMA-GROUP est une entreprise spécialisée en sécurité informatique. PROCSIMA-GROUP aide les entreprises à protéger leurs informations et leurs données contre les attaques externes et internes de toute nature, et à assurer la bonne performance de leurs systèmes ainsi que la bonne disponibilité de leurs services.

Située à Louvain-la-Neuve et composée d’une quinzaine de consultants, PROCSIMA-GROUP vise à devenir le leader belge de la cyber protection en fournissant des services, de la consultance et des solutions à haute valeur ajoutée, tels que : services d’audit & reviews, protection des données, stratégie, architecture, gouvernance, GDPR, etc.

Pour de plus amples informations, veuillez consulter http://www.procsima-group.eu.

Afin de renforcer l’équipe, nous sommes activement à la recherche (CDI ou freelance) d’un(e) :

Project Manager
Sécurité/Infrastructure/Réseau

Responsabilités :

En tant que Project Manager – Sécurité/Infrastructure/Réseau, votre mission est de gérer de bout en bout les projets sécurité dans le domaine de l’infrastructure et du réseau.

Vos principales responsabilités sont les suivantes :

  • Coordonner toutes les activités tout au long des différentes phases du projet.
  • Livrer les livrables requis en accord avec les objectifs budgétaires, de qualité et de timing.
  • Appliquer la méthodologie demandée par le client (Waterfall, Agile/Scrum, DevOps, etc.).
  • Contrôler le scope et la viabilité du business case tout au long du projet.
  • Fédérer les équipes projet et favoriser la communication entre les différentes parties prenantes.
  • Rapporter l’évolution des démarches de manière régulière et structurée vers la hiérarchie.
Profil :
  • Vous disposez d’une à trois années d’expérience dans une position similaire. Les profils juniors sont également les bienvenus.
  • Vous avez une bonne connaissance générale de l’infrastructure (Windows, Linux, Unix) et des réseaux (LAN Cisco, WAN, Wifi). Connaissance en design des architectures réseau est un atout.
  • Vous possédez une bonne connaissance générale de la sécurité des réseaux et de l’infra (antivirus, firewalls, proxys, IDS/IPS, antispams, APT prevention systems, etc.).
  • Vous maitrisez la gestion de projet (Prince2 ou PMI), et avez une bonne compréhension d’Agile, Scrum et/ou Waterfall.
  • Vous êtes pragmatique, organisé(e), autonome, et doté(e) d’un bon esprit d’analyse et de synthèse.
  • Vous faites montre de leadership, de proactivité et aimez coordonner des projets.
  • Vous faites preuve d’un esprit d’équipe développé et avez de bonnes compétences communicationnelles et d’écoute.
  • Vous communiquez aisément en français. La connaissance de l’anglais/néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer en fonction des missions (Bruxelles, Wallonie).
Offre :
  • Intégrer une entreprise en pleine croissance proposant des solutions innovantes et variées.
  • Une fonction challengeante et diversifiée dans un secteur en plein développement.
  • L’opportunité de travailler sur divers projets pour le compte de différents clients.
  • La possibilité de travailler sous contrat à durée indéterminée ou en tant que freelance.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs en phase avec votre expérience.
  • Un plan de formation aligné sur des objectifs de développement clairs.

Responsable QHSE - Energie - Dunkerque

Dunkerque LNG (Dunkerque Liquefied Gaz Naturel) est une filiale à 65 % du groupe EDF SA, 25 % de l’opérateur belge Fluxys et 10 % de Total. L’exploitant du terminal méthanier de Dunkerque est Gaz-OPALE, filiale d’exploitation de Dunkerque LNG.

GAZ-OPALE est en charge de la conduite, de la maintenance et du respect des exigences HSE (Hygiène Sécurité et Environnement). Le terminal méthanier est un site ICPE (Installation Classée pour la Protection de l’Environnement) qui suit la directive SEVESO III seuil haut.

Responsable QHSE

Responsabilités :

En tant que Responsable QHSE, votre mission est de définir et coordonner la politique «qualité, hygiène, sécurité et environnement» de l’ensemble du terminal méthanier. Pour ce faire, vous pouvez compter sur une équipe de 2 personnes et sur un réseau de partenaires externes. Rapportant au Directeur d’Exploitation, vous faites partie du Comité de Direction de Dunkerque LNG.

Vos principales responsabilités sont les suivantes :

  • Implémenter et coordonner le système de gestion de la sécurité : élaboration des plans d’urgence et mise en œuvre d’exercices.
  • Coordonner la sécurité du site, gérer et analyser les événements et incidents.
  • Évaluer et sensibiliser aux risques des postes de travail.
  • Participer au Comité d’Hygiène, de Sécurité et des Conditions de Travail (CHSCT).
  • Obtenir la triple certification Iso 9001, 14001, OHSAS 18001 par la mise en œuvre de documents contrôlés.
  • Garantir la mise en œuvre des évolutions réglementaires et assurer la gestion des déchets.
  • Veiller à la bonne application des règles d’accès au site.
  • Participer aux astreintes de la cellule de crise opérationnelle à raison d’une semaine sur cinq.
Profil :
  • Vous êtes titulaire d’un Bac+5 QHSE, scientifique, ou équivalent par expérience.
  • Vous possédez une expérience réussie de 5 à 10 ans en tant que Responsable QHSE d’un site industriel type SEVESO. Une première expérience en management est un plus.
  • Vous communiquez aisément en français et en anglais.
  • Vous êtes autonome, rigoureux(se) et faites preuve d’un esprit d’ouverture, d’écoute et de synthèse.
  • Vous appréciez le travail d’équipe et possédez une grande aisance relationnelle.
  • Vous êtes habitué(e) à travailler dans un environnement structuré et exigeant (ISO 9001-14001, OHSAS 18001).
  • Vous êtes basé(e) dans les environs de Dunkerque et êtes disposé(e) à vous déplacer ponctuellement en France et à l’étranger (Bruxelles, Zeebrugge, etc.)
Offre :
  • Une fonction stimulante au sein d’un environnement diversifié.
  • L’opportunité de rejoindre un acteur majeur dans l’industrie du gaz en Europe.
  • Des challenges et des contacts variés au sein et en dehors de l’organisation.
  • Des opportunités de développement et de formations.
  • Un salaire attractif reprenant des avantages extra-légaux avantageux.

Senior Project Manager Sécurité/Infrastructure/Réseau - IT & Consultancy Solutions - Louvain-la-Neuve

Fondée en 2015, PROCSIMA-GROUP est une entreprise spécialisée en sécurité informatique. PROCSIMA-GROUP aide les entreprises à protéger leurs informations et leurs données contre les attaques externes et internes de toute nature, et à assurer la bonne performance de leurs systèmes ainsi que la bonne disponibilité de leurs services.

Située à Louvain-la-Neuve et composée d’une quinzaine de consultants, PROCSIMA-GROUP vise à devenir le leader belge de la cyber protection en fournissant des services, de la consultance et des solutions à haute valeur ajoutée, tels que : services d’audit & reviews, protection des données, stratégie, architecture, gouvernance, GDPR, etc.

Pour de plus amples informations, veuillez consulter http://www.procsima-group.eu.

Afin de renforcer l’équipe, nous sommes activement à la recherche (CDI ou freelance) d’un(e) :

Senior Project Manager
Sécurité/Infrastructure/Réseau

Responsabilités :

En tant que Senior Project Manager – Sécurité/Infrastructure/Réseau, votre mission est de gérer de bout en bout les projets sécurité dans le domaine de l’infrastructure et du réseau.

Vos principales responsabilités sont les suivantes :

  • Coordonner toutes les activités du projet tout au long des différentes phases du projet.
  • Livrer les livrables requis en accord avec les objectifs budgétaires, de qualité et de timing.
  • Appliquer la méthodologie demandée par le client (Waterfall, Agile/Scrum, DevOps, etc.).
  • Contrôler le scope et la viabilité du business case tout au long du projet.
  • Fédérer les équipes projet et favoriser la communication entre les différentes parties prenantes.
  • Rapporter l’évolution des démarches de manière régulière et structurée vers la hiérarchie.
Profil :
  • Minimum 5 ans d’expérience dans une position similaire en infrastructure et sécurité, dont 3 ans en Project Management.
  • Vous avez une bonne connaissance générale de l’infrastructure (Windows, Linux, Unix) et des réseaux (LAN Cisco, WAN, Wifi). Connaissance en design des architectures réseau est un atout.
  • Vous possédez une bonne connaissance de la sécurité des réseaux et de l’infra (antivirus, firewalls, proxys, IDS/IPS, antispams, APT prevention systems, etc.).
  • Vous maitrisez la gestion de projet (Prince2 ou PMI), et avez une bonne compréhension d’Agile, Scrum et/ou Waterfall.
  • Vous êtes pragmatique, organisé(e), autonome, et doté(e) d’un bon esprit d’analyse et de synthèse.
  • Vous faites montre de leadership, de proactivité et aimez coordonner des projets et des programmes.
  • Vous faites preuve d’un esprit d’équipe développé et avez de bonnes compétences communicationnelles et d’écoute.
  • Vous communiquez aisément en français. La connaissance de l’anglais/néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer en fonction des missions (Bruxelles, Wallonie).
Offre :
  • Intégrer une entreprise en pleine croissance proposant des solutions innovantes et variées.
  • Une fonction diversifiée où il faut relever des défis dans un secteur en plein développement.
  • L’opportunité de travailler sur divers projets pour le compte de différents clients.
  • La possibilité de travailler sous contrat à durée indéterminée ou en tant que freelance.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs en phase avec votre expérience.
  • Un plan de formation aligné sur des objectifs de développement clairs.

Embedded Software Developer/Engineer - Engineering - Luxembourg

Créée en 2008, ShifTech Engineering est une entreprise spécialisée dans le domaine de la préparation de moteur sur banc de puissance. Composée d’une équipe de 15 personnes, ShifTech Engineering est actuellement présente en Belgique, en France, au Luxembourg et en Chine, et jouit d’une renommée internationale pour la qualité de ses réalisations et services destinés aux particuliers. Pour plus d’informations sur l’entreprise, veuillez consulter www.shiftech.eu.

Shiftech Engineering développe depuis 3 ans un nouveau produit hardware. Celui-ci permet au préparateur du monde entier de lire puis d’écrire les données d’un calculateur moteur. Pour plus d’informations sur le produit, veuillez consulter www.autotuner-tool.com

Dans le cadre du renforcement de l’équipe de Shiftech Engineering au Luxembourg, nous sommes activement à la recherche d’un (m/f) :

Embedded Software Developer/Engineer

Responsabilités :

En collaboration avec le chef de projet et notre Ingénieur Firmware, vous participez aux activités de développement de l’outil Autotuner. Vos principales responsabilités sont :

  • Analyser, développer et améliorer le code C déjà existant suivant les développements de nouveaux calculateurs moteur.
  • Etre en charge du développement des scripts LUA suivant le protocole CAN de la voiture.
  • Rapporter et présenter de manière structurée, rigoureuse et adaptée les résultats des activités.
  • Effectuer du reverse engineering.
Profil :
  • Vous disposez d’un Master en IT ou électronique.
  • Vous jouissez, idéalement, de 3 à 5 années d’expérience dans une fonction de développement Firmware en milieu industriel ou équivalent.
  • Vous possédez une excellente maîtrise de Python et du langage C. La connaissance des scripts LUA et de FreeRTOS est un atout majeur.
  • Vous êtes à l’aise avec Git ou tout autre logiciel de gestion de sources.
  • Vous faites montre d’un bel intérêt pour l’esprit start-up qui encourage la créativité et l’innovation.
  • Vous aimez les challenges et vous montrez de réelles affinités pour les innovations technologiques.
  • Vous communiquez aisément en français et en anglais.
  • Vous êtes analytique, proactif(ve), autonome, organisé(e) et rigoureux(se).
Offre :
  • Une fonction technique diversifiée et stimulante dans une petite équipe jeune et dynamique.
  • Intégrer une structure en pleine expansion et de renommée dans le domaine automobile pour la qualité de ses services.
  • Un cadre de travail agréable et d’accès aisé, et la possibilité de homeworking.
  • Un contrat à durée indéterminée à temps plein au Luxembourg, à Redange-sur-Attert.
  • Des opportunités de formation et de développement.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs comprenant entre autres une voiture de société.

Security Management Consultant - IT & Consultancy Solutions - Louvain-la-Neuve

Fondée en 2015, PROCSIMA-GROUP est une entreprise spécialisée en sécurité informatique. PROCSIMA-GROUP aide les entreprises à protéger leurs informations et leurs données contre les attaques externes et internes de toute nature, et à assurer la bonne performance de leurs systèmes ainsi que la bonne disponibilité de leurs services.

Située à Louvain-la-Neuve et composée d’une quinzaine de consultants, PROCSIMA-GROUP vise à devenir le leader belge de la cyber protection en fournissant des services, de la consultance et des solutions à haute valeur ajoutée, tels que : services d’audit & reviews, protection des données, stratégie, architecture, gouvernance, GDPR, etc.

Pour de plus amples informations, veuillez consulter http://www.procsima-group.eu.

Afin de renforcer l’équipe, nous sommes activement à la recherche (CDI ou freelance) d’un(e) :

Security Management Consultant

Responsabilités :

En tant que Security Management Consultant, vos principales responsabilités sont les suivantes :

  • Réaliser des audits et études sur l’état du système de gestion de la sécurité des entreprises (ISMS).
  • Conseiller le client en fournissant des recommandations concrètes.
  • Proposer au client une feuille de route et une stratégie à court, moyen et long terme.
  • Accompagner le client dans ses projets d’amélioration et à la mise en place de la stratégie.
  • S’assurer que la gouvernance est mise en place de manière effective au niveau opérationnel ainsi que dans tous les départements de l’entreprise.
  • Participer à des projets en tant que conseiller, coach et rédacteur des politiques et processus de gestion de la sécurité.
  • Conduire et effectuer des campagnes de sensibilisation et de formation des employés.
Profil :
  • Vous disposez d’une à trois années d’expérience dans une position similaire. Les profils juniors sont également les bienvenus.
  • Vous possédez une bonne connaissance générale des systèmes de sécurité (firewalls, proxys, IDS/IPS, SIEM, IAM, cryptographie, etc.) ainsi que de l’Ethical Hacking.
  • Vous maitrisez la gestion de projet (Prince2, PMI ou Agile), et avez une bonne connaissance des systèmes de gouvernance ITIL et CobiT. Une certification CISM ou CISSP est un sérieux atout.
  • Vous êtes pragmatique, organisé(e), autonome, et doté(e) d’un bon esprit d’analyse et de synthèse.
  • Vous possédez de bonnes capacités rédactionnelles (rédaction de documents clairs et concis).
  • Vous faites montre de leadership, de proactivité et aimez coordonner des projets.
  • Vous faites preuve d’un esprit d’équipe développé et avez de bonnes compétences communicationnelles et d’écoute.
  • Vous communiquez aisément en français. La connaissance de l’anglais/néerlandais est un atout.
  • Vous êtes disposé(e) à vous déplacer en fonction des missions (Bruxelles, Wallonie).
 Offre :
  • Intégrer une entreprise en pleine croissance proposant des solutions innovantes et variées.
  • Une fonction challengeante et diversifiée dans un secteur en plein développement.
  • L’opportunité de travailler sur divers projets pour le compte de différents clients.
  • La possibilité de travailler sous contrat à durée indéterminée ou en tant que freelance.
  • Une offre salariale attrayante, assortie d’avantages extralégaux compétitifs en phase avec votre expérience.
  • Un plan de formation aligné sur des objectifs de développement clairs.