196 520 Emplois - Belgique

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

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

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

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

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

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