73 099 Emplois - Belgique

Our Purpose

Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we’re helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential.

Title and Summary

Corporate Security Responsibility

All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must:

• Abide by Mastercard’s security policies and practices;

• Ensure the confidentiality and integrity of the information being accessed;

• Report any suspected information security violation or breach, and

• Complete all periodic mandatory security trainings in accordance with Mastercard’s guidelines.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Position Description Summary

The primary purpose of this role is to support the Lead, EU, GRASP in advancement of regulatory science, policy and intelligence for EU region. This will be achieved in close collaboration with the Head of Global Regulatory Science & Policy, NA and APAC regional function leads, and internal global regulatory teams (e.g., shaping CSL positions), as well as through external engagement (e.g., enhancing CSL’s visibility and influence in the regulatory landscape). The incumbent will monitor and analyze regulatory trends, changes, and developments to inform strategic decision-making and maintain a competitive edge for CSL. In addition, the incumbent will maintain and enhance operational aspects of the role, including but not limited to the enhancement and maintenance of GRASP SharePoint and related processes.  The scope of this role is intentionally broad and may evolve over time in response to shifting business priorities and emerging opportunities.

Main Responsibilities & Accountabilities

• Advance Regulatory Science, Policy, and Intelligence

Support the development of regulatory science, policy, and intelligence initiatives and contribute to shaping the regulatory environment for assigned platforms, business units, or topics. Help identify opportunities for non-product-specific collaboration with global health authorities. Collaborate with Global Regulatory Affairs (GRA), regional leads, and relevant teams to support the planning and execution of external engagement strategies. Represent CSL in select industry groups, professional associations, and other external forums, ensuring meaningful and well-prepared contributions. Provide regulatory science input for internal strategy discussions and help align regulatory policy goals with business objectives.

• Regulatory Intelligence & Communication

Monitor, analyze, and share key regulatory trends and developments that could impact CSL’s platforms or focus areas. Contribute to regular updates, reports, and other communications that support regulatory decision-making and knowledge sharing across the organization. Support assessments of new and draft regulations or guidance, contribute to CSL’s response and position, and align action plans with key stakeholders. Assist in identifying and prioritizing regulatory risks and opportunities, working closely with internal subject matter experts.

• Collaboration & Execution

Contribute to the development and tracking of the Regulatory Policy Roadmap and support measuring progress through KPIs.

Work with regional leads, internal regulatory teams, and other functions such as Public and Government Affairs (PAGA) to align efforts and share insights.

Engage with external partners or consultants, as needed, to support intelligence gathering and dissemination activities.

• Operations & Process

Maintain and further advance operational and process related activities within Regulatory Policy and Intelligence function.

Qualifications & Experience Requirements

• Bachelor’s degree in Life Sciences, Medical Science, Pharmacy, or a related field.

• Minimum of 3 years of experience in the life sciences industry, with exposure to regulatory affairs or a related function.

• Understanding of regulatory requirements across product development and post-marketing phases; prior hands-on regulatory experience is preferred.

• Familiarity with EU regulatory systems; additional global exposure is an advantage.

• Experience contributing to regulatory intelligence or policy work is beneficial.

• Previous interaction with regulatory agencies such as EMA is a plus.

• Strong communication skills in English, both written and verbal, with the ability to present information clearly and concisely.

• Proficiency with digital tools such as ChatGPT and Microsoft Copilot, along with a strong understanding of current AI trends, is preferred.

• Demonstrates strategic thinking with a developing business awareness.

• Collaborative mindset, with the ability to build effective working relationships and networks.

• Proactive, adaptable, and comfortable working in a cross-functional, multicultural environment.

• Willingness to travel internationally up to 20% of the time.

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma . Our parent company, CSL , headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL

VERTEGENWOORDIGER INDUSTRIE (M/V/X) voor de regio Ostflandern

Wat wij jou bieden:

• Een aantrekkelijk salaris met commissiesysteem, aangevuld met extra voordelen (auto van de zaak, onkostenvergoeding, smartphone en tablet).
• Een afwisselende baan in een dynamische markt.
• Professionele ondersteuning en een grondige introductietraining.Constante ondersteuning van je salesmanager en het interne salesteam

Dat is hun taak:

• Je versterkt bestaande klantenrelaties en gaat actief op zoek naar nieuwe klanten.
• Je ontwikkelt je verkoopgebied voortdurend.
• Je adviseert klanten over producten en de toepassing ervan aan de hand van presentaties en demonstraties.

Wat je meebrengt

• Je hebt technische affiniteit, denkt probleemoplossend en bent proactief.
• Je hebt een commerciële instelling en bent enthousiast over het vinden van maatwerkoplossingen voor onze klanten.
• Je hebt ervaring in sales en in het opbouwen en onderhouden van klantrelaties.
• Je hebt een rijbewijs klasse B.

VERTEGENWOORDIGER INDUSTRIE (M/V/X) voor de regio Zaventem - Londerzeel

Wat wij jou bieden:

• Een aantrekkelijk salaris met commissiesysteem, aangevuld met extra voordelen (auto van de zaak, onkostenvergoeding, smartphone en tablet).
• Een afwisselende baan in een dynamische markt.
• Professionele ondersteuning en een grondige introductietraining.Constante ondersteuning van je salesmanager en het interne salesteam

Dat is hun taak:

• Je versterkt bestaande klantenrelaties en gaat actief op zoek naar nieuwe klanten.
• Je ontwikkelt je verkoopgebied voortdurend.
• Je adviseert klanten over producten en de toepassing ervan aan de hand van presentaties en demonstraties.

Wat je meebrengt

• Je hebt technische affiniteit, denkt probleemoplossend en bent proactief.
• Je hebt een commerciële instelling en bent enthousiast over het vinden van maatwerkoplossingen voor onze klanten.
• Je hebt ervaring in sales en in het opbouwen en onderhouden van klantrelaties.
• Je hebt een rijbewijs klasse B.

Telefonisch technische verkoper (m/v/x) - Fulltime of parttime (20 tot 38 uur per week)

Als strategische aanvulling op onze buitendienst en webshop zijn we op zoek naar een telefonisch verkoper met gezonde basis technische kennis (20 tot 38,5 uur). Krijg je energie van waarde creëren voor en het helpen van klanten? En werk je graag in een team? Dan is dit de perfecte job voor jou!

WAT WIJ BIEDEN?

• Een aantrekkelijk salarismodel met bonusstructuur
• Vaste werktijden vanaf 20 uur per week (parttime) tot 38 uur (fulltime)
• Thuiswerken mogelijk
• Geen weekenddiensten, late diensten of ploegendiensten
• Een grondig inwerktraject (onboarding) met verkoop-/producttraining
• Een open, op vertrouwen gebaseerde werksfeer, korte besluitvormingsprocessen, goede mogelijkheden om het bedrijf mee vorm te geven en interessante carrièremogelijkheden!
• Personeelsvoordelen en vakantiegeld
• Wervingsbonussen als je nieuwe collega’s aanwerft

WAT GA JE DOEN?

• Actieve verkoop van onze TECHNOLIT®- producten via de telefoon aan zakelijke klanten (B2B)
• Support voor bestaande klanten
• Zorgen voor klanttevredenheid en klantenbinding
• Meedenken over onze interne verkoopprocessen en daaraan meewerken
• Documenteren van alle klantgegevens en gespreksinhoud

WAT BRENG JE MEE?

• Je vindt het leuk om te bellen
• Je bent communicatief, persoonlijk en hebt een open houding
• Je hebt een zelfstandige en gestructureerde manier van werken
• Je hebt een commerciële instelling en bent enthousiast in het zoeken naar oplossingen op maat van onze klanten.
• Je bent gemotiveerd en vindt het leuk om samen in teamverband successen te vieren
• Je hebt een goede beheersing van geschreven en gesproken Nederlands. Engels en Duits zijn een pre.

Are you passionate about ensuring the highest standards of quality and regulatory compliance in a dynamic environment? Do you excel at building strong supplier relationships and driving continuous improvement? If so, we have an exciting opportunity for you to join our team as a Supplier Quality Engineer  in Brussels, Belgium.

This is your chance to contribute to impactful work in the medical device industry, where your expertise will directly support our mission of improving lives through innovation and quality.

What to Expect:

Supplier Quality Oversight

• Executing activities to ensure compliance with regulatory standards and the Quality Management System.
• Conducting technical reviews of suppliers to assess their capability to manufacture materials and meet required standards.
• Overseeing, assessing, and monitoring supplier performance in areas like manufacturing, process control, quality control practices, corrective actions, and continuous improvement.

Production Part Approval Process (PPAP)

• Defining and approving PPAP requirements for new and revised purchased parts, ensuring their on-time completion.

Supplier Issue Management

• Issuing and following up on Agile Quality figures like SCARs, SACAs, and NCEs related to suppliers, ensuring workflows comply with established KPIs.
• Collaborating with suppliers on problem-solving, root cause analysis, and implementing corrective actions to avoid repeat issues.
• Resolving day-to-day quality issues with suppliers by addressing non-conformities and coordinating material disposition (e.g., returns, rework, sorting).

Cross-Functional Collaboration

• Partnering with departments like Post Market Surveillance, Quality Engineering, Manufacturing Engineering, and R&D to address supplier-related complaints and challenges.

Audits and Documentation

• Maintaining complete and accurate supplier quality records, ensuring compliance with regulatory standards.
• Supporting audits as a subject matter expert, with occasional travel required.

Training and Development

• Continuously training on applicable procedures to stay up-to-date with regulations and quality standards.

Gemba Mindset

• Going to the “Gemba” (where the action is) to understand the root cause of problems and implement practical solutions.

What We Expect:

Qualifications & Knowledge:

• Education:  Bachelor’s degree in Engineering (Biochemical, Chemical, or related field). An ASQ Supplier Quality Engineer Certificate is a plus.
• Regulatory Expertise:  Knowledge of EU MDR/IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus.
• Industry Experience:  5+ years’ experience in medical device manufacturing or a related industry, with 3+ years in a Quality function preferred.
• Problem Solving:  Proficiency with problem-solving tools such as SPC, Total Quality Management, and root cause analysis.
• Strong Communicator:  Ability to effectively communicate at all levels of the organisation, both written and verbal.
• Analytical Mindset:  Skilled at analyzing data, evaluating factors, and translating insights into actionable plans.
• Self-Motivated:  Able to work independently with minimal supervision, while managing multiple complex projects.

Why Hologic?

• Work on impactful projects that make a difference in the medical device industry.
• Build relationships with suppliers around the globe, develop your skills and grow your career in a supportive and collaborative environment.
• Competitive salary and benefits package, including health insurance

Travel Requirements:  15-20%
Language Requirements:  Proficient in English (written and oral). A second language is a plus.

#LI-HE1

Are you passionate about ensuring the highest standards of quality and regulatory compliance in a dynamic environment? Do you excel at building strong supplier relationships and driving continuous improvement? If so, we have an exciting opportunity for you to join our team as a Supplier Quality Engineer  in Brussels, Belgium.

This is your chance to contribute to impactful work in the medical device industry, where your expertise will directly support our mission of improving lives through innovation and quality.

What to Expect:

Supplier Quality Oversight

• Executing activities to ensure compliance with regulatory standards and the Quality Management System.
• Conducting technical reviews of suppliers to assess their capability to manufacture materials and meet required standards.
• Overseeing, assessing, and monitoring supplier performance in areas like manufacturing, process control, quality control practices, corrective actions, and continuous improvement.

Production Part Approval Process (PPAP)

• Defining and approving PPAP requirements for new and revised purchased parts, ensuring their on-time completion.

Supplier Issue Management

• Issuing and following up on Agile Quality figures like SCARs, SACAs, and NCEs related to suppliers, ensuring workflows comply with established KPIs.
• Collaborating with suppliers on problem-solving, root cause analysis, and implementing corrective actions to avoid repeat issues.
• Resolving day-to-day quality issues with suppliers by addressing non-conformities and coordinating material disposition (e.g., returns, rework, sorting).

Cross-Functional Collaboration

• Partnering with departments like Post Market Surveillance, Quality Engineering, Manufacturing Engineering, and R&D to address supplier-related complaints and challenges.

Audits and Documentation

• Maintaining complete and accurate supplier quality records, ensuring compliance with regulatory standards.
• Supporting audits as a subject matter expert, with occasional travel required.

Training and Development

• Continuously training on applicable procedures to stay up-to-date with regulations and quality standards.

Gemba Mindset

• Going to the “Gemba” (where the action is) to understand the root cause of problems and implement practical solutions.

What We Expect:

Qualifications & Knowledge:

• Education:  Bachelor’s degree in Engineering (Biochemical, Chemical, or related field). An ASQ Supplier Quality Engineer Certificate is a plus.
• Regulatory Expertise:  Knowledge of EU MDR/IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus.
• Industry Experience:  5+ years’ experience in medical device manufacturing or a related industry, with 3+ years in a Quality function preferred.
• Problem Solving:  Proficiency with problem-solving tools such as SPC, Total Quality Management, and root cause analysis.
• Strong Communicator:  Ability to effectively communicate at all levels of the organisation, both written and verbal.
• Analytical Mindset:  Skilled at analyzing data, evaluating factors, and translating insights into actionable plans.
• Self-Motivated:  Able to work independently with minimal supervision, while managing multiple complex projects.

Why Hologic?

• Work on impactful projects that make a difference in the medical device industry.
• Build relationships with suppliers around the globe, develop your skills and grow your career in a supportive and collaborative environment.
• Competitive salary and benefits package, including health insurance

Travel Requirements:  15-20%
Language Requirements:  Proficient in English (written and oral). A second language is a plus.

#LI-HE1

Quality Assurance Engineer, Distribution (EMEA)

Role location : Zaventem, Belgium

Travel: 10-15%

At Hologic, we are driven by our purpose to enable healthier lives everywhere, every day. As a leader in medical technology, we are dedicated to improving health outcomes through innovation, integrity and uncompromising quality.

We are now looking for an experienced Quality Assurance Engineer to join our team in Zaventem, Belgium. As Quality Assurance Engineer specializing in distribution, you will play a vital role in upholding product integrity across the supply chain. You will be responsible for managing distributor relationships, implementing robust quality assurance measures and ensuring full compliance with regulatory requirements, quality standards and Good Distribution Practices (GDP).

Role Responsibilities:

• Distributor Management: evaluate and oversee new and existing distributors to ensure they meet both regulatory and organizational requirements
• Quality Compliance: ensure audits, validations, and other quality activities are completed to maintain the effectiveness of Hologic’s Quality System
• Cross-Functional Collaboration: work closely with Regulatory Affairs and other departments to identify local distribution requirements and ensure compliance regarding product storage, handling, transportation, traceability and reporting
• Documentation & Reporting: maintain comprehensive records of distributor compliance, including assessments, quality agreements, audits, and corrective actions
• Risk & Non-Conformance Management: investigate non-conformances and implement corrective and preventive actions to eliminate re-occurrence
• Stakeholder Engagement: serve as the primary contact for distributor quality-related inquiries, providing expert guidance and regular updates 
• Continuous Improvement: develop and track metrics and KPIs to monitor distributor quality performance and support ongoing improvement initiatives
• SOP Development: participate in the creation and maintenance of SOPs related to distribution activities
• Audit Support: provide QA expertise during internal and external audits

Knowledge, skills and experience: 

• Background in Engineering, Quality Assurance, Supply Chain Management, Logistics or a related field
• Experience in medical device manufacturing or a related industry, ideally in a quality-focused role
• Knowledge of Good Distribution Practices (GDP), ISO 9001/13485, EU MDR/IVDR and medical device regulations
• Proven experience in root cause analysis, risk assessment, CAPA and audit processes
• Experience with logistics and distribution processes will be advantageous
• Excellent communication, negotiation and interpersonal skills—able to engage effectively with both internal and external stakeholders
• Analytical and problem-solving mindset with a proactive and organized approach to managing multiple priorities
• Adaptability to change and the ability to work both independently and as part of a collaborative team

If you’re excited by the opportunity to leverage your quality assurance expertise in a fast-paced, mission-driven company, we want to hear from you. Apply today and join us at Hologic!

#LI-KP1

#associate

Are you passionate about ensuring the highest standards of quality and regulatory compliance in a dynamic environment? Do you excel at building strong supplier relationships and driving continuous improvement? If so, we have an exciting opportunity for you to join our team as a Supplier Quality Engineer  in Brussels, Belgium.

This is your chance to contribute to impactful work in the medical device industry, where your expertise will directly support our mission of improving lives through innovation and quality.

What to Expect:

Supplier Quality Oversight

• Executing activities to ensure compliance with regulatory standards and the Quality Management System.
• Conducting technical reviews of suppliers to assess their capability to manufacture materials and meet required standards.
• Overseeing, assessing, and monitoring supplier performance in areas like manufacturing, process control, quality control practices, corrective actions, and continuous improvement.

Production Part Approval Process (PPAP)

• Defining and approving PPAP requirements for new and revised purchased parts, ensuring their on-time completion.

Supplier Issue Management

• Issuing and following up on Agile Quality figures like SCARs, SACAs, and NCEs related to suppliers, ensuring workflows comply with established KPIs.
• Collaborating with suppliers on problem-solving, root cause analysis, and implementing corrective actions to avoid repeat issues.
• Resolving day-to-day quality issues with suppliers by addressing non-conformities and coordinating material disposition (e.g., returns, rework, sorting).

Cross-Functional Collaboration

• Partnering with departments like Post Market Surveillance, Quality Engineering, Manufacturing Engineering, and R&D to address supplier-related complaints and challenges.

Audits and Documentation

• Maintaining complete and accurate supplier quality records, ensuring compliance with regulatory standards.
• Supporting audits as a subject matter expert, with occasional travel required.

Training and Development

• Continuously training on applicable procedures to stay up-to-date with regulations and quality standards.

Gemba Mindset

• Going to the “Gemba” (where the action is) to understand the root cause of problems and implement practical solutions.

What We Expect:

Qualifications & Knowledge:

• Education:  Bachelor’s degree in Engineering (Biochemical, Chemical, or related field). An ASQ Supplier Quality Engineer Certificate is a plus.
• Regulatory Expertise:  Knowledge of EU MDR/IVDR, CFR820, ISO 13485, Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus.
• Industry Experience:  5+ years’ experience in medical device manufacturing or a related industry, with 3+ years in a Quality function preferred.
• Problem Solving:  Proficiency with problem-solving tools such as SPC, Total Quality Management, and root cause analysis.
• Strong Communicator:  Ability to effectively communicate at all levels of the organisation, both written and verbal.
• Analytical Mindset:  Skilled at analyzing data, evaluating factors, and translating insights into actionable plans.
• Self-Motivated:  Able to work independently with minimal supervision, while managing multiple complex projects.

Why Hologic?

• Work on impactful projects that make a difference in the medical device industry.
• Build relationships with suppliers around the globe, develop your skills and grow your career in a supportive and collaborative environment.
• Competitive salary and benefits package, including health insurance

Travel Requirements:  15-20%
Language Requirements:  Proficient in English (written and oral). A second language is a plus.

#LI-HE1