Quality Assurance and Regulatory Affairs Engineer

il y a 3 semaines


Lille, Hauts-de-France Celeos SAS Temps plein
Celeos SAS: Quality Assurance and Regulatory Affairs Engineer

We are seeking a highly skilled Quality Assurance and Regulatory Affairs Engineer to join our team at Celeos SAS. As a key member of our organization, you will play a crucial role in ensuring the quality and regulatory compliance of our medical devices.

Key Responsibilities:
  • Develop and implement quality management systems to ensure compliance with regulatory requirements
  • Contribute to the development of our regulatory roadmap and coordinate medical device validation projects
  • Support the management and optimization of laboratory information management systems and electronic lab notebooks
  • Participate in the preparation for CE marking and ISO 14845 certification of our medical devices
Requirements:
  • Ongoing Master's degree in a relevant field such as Life Sciences, Pharma, Biomedical Engineering, or Regulatory Affairs
  • Strong understanding and knowledge of quality concepts, professional practices, and quality assurance
  • Proficiency in statistical analysis with univariate and multivariate methods
  • Notions in Public health and health law
  • Medical Devices: general principles in design and distribution
  • Proficiency in English; French is a plus
About Us:

Celeos SAS is an innovative medical device manufacturer committed to improving human and animal health while minimizing our environmental footprint. We are a purpose-driven company that values creativity, productivity, and flexibility.

This is a full-time position with a mix of on-site and remote work. We offer a healthy and fulfilling work environment that nurtures both creativity and productivity while fostering flexibility. If you are a motivated and detail-oriented individual with a passion for quality assurance and regulatory affairs, we encourage you to apply.



  • Lille, Hauts-de-France Celeos SAS Temps plein

    About Celeos SASCeleos SAS is a pioneering medical device manufacturer specializing in oncology solutions for human surgical applications. Our innovative technology enables real-time assistance to surgeons, minimizing incomplete tumor removals and improving patient outcomes.Job Title: Quality Assurance and Regulatory Affairs EngineerWe are seeking a highly...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    About Celeos SASCeleos SAS is an innovative medical device manufacturer focused on the oncology segment for human surgical applications. Our mission is to improve human and animal health while minimizing our environmental footprint.Job DescriptionWe are seeking a Quality Assurance and Regulatory Affairs Engineer to join our team. As a key member of our...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    Celeos SAS: A Purpose-Driven CompanyWe are an innovative medical device manufacturer acting predominantly in the oncology segment for human surgical applications. Our mission is to minimize incomplete tumour removals, resulting in improved patient outcomes and enhanced quality of life.About the RoleWe are seeking a Quality Assurance and Regulatory Affairs...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    Quality Assurance and Regulatory Affairs Engineer ApprenticeCeleos SAS is an innovative medical device manufacturer with a strong presence in the oncology segment for human surgical applications. We are committed to improving human and animal health while minimizing our environmental footprint.About the RoleWe are seeking a Quality Assurance and Regulatory...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    About Celeos SASCeleos SAS is a dynamic and innovative medical device manufacturer operating primarily in the oncology segment for human surgical applications. We are committed to improving human and animal health and their well-being while minimizing our environmental footprint.Job DescriptionWe are seeking a Quality Assurance and Regulatory Affairs...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    Quality Assurance and Regulatory Affairs Engineer ApprenticeCeleos SAS is an innovative medical device manufacturer acting predominantly in the oncology segment for human surgical applications. We are committed to improving human and animal health and their well-being while minimizing our environmental footprint.About the RoleWe are seeking a Quality...


  • Lille, Hauts-de-France Celeos SAS Temps plein

    About Celeos SASCeleos SAS is an innovative medical device manufacturer operating primarily in the oncology segment for human surgical applications. Our company is committed to improving human and animal health while minimizing our environmental footprint.Job DescriptionWe are seeking a Quality Assurance and Regulatory Affairs Engineer Apprentice to join our...

  • Quality Assurance Specialist

    il y a 2 semaines


    Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for clients in the life sciences industry, providing expert services in regulatory affairs, quality and compliance, vigilance, and medical information. With a global reach and local expertise, we support clients throughout the product lifecycle, from established products to...

  • Regulatory Affairs Specialist

    il y a 3 semaines


    Lille, Hauts-de-France Excelya Temps plein

    Excelya, a leading contract research organization (CRO), is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will play a key role in ensuring compliance with regulatory requirements and ensuring the quality and integrity of our clinical trials.MissionCMC:Develop and implement the strategy for...

  • Quality Assurance Specialist

    il y a 3 semaines


    Lille, Hauts-de-France Groupe ProductLife Temps plein

    Qualification and Validation ConsultantWe are seeking a highly skilled Qualification and Validation Consultant to join our team at Groupe ProductLife. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of quality and compliance in our operations.Key Responsibilities:Manage periodic qualification and...

  • Quality Assurance Specialist

    il y a 3 semaines


    Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for clients in the life sciences industry, providing expert services in regulatory affairs, quality and compliance, vigilance, and medical information. With a global reach and local expertise, we support clients throughout the product lifecycle, from established products to...

  • Quality Assurance Specialist

    il y a 2 semaines


    Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for clients in the life sciences industry, providing expert services in regulatory affairs, quality and compliance, vigilance, and medical information. With a global reach and local expertise, we support clients throughout the product lifecycle, from established products to...

  • Quality Assurance Specialist

    il y a 3 semaines


    Lille, Hauts-de-France Groupe ProductLife Temps plein

    Qualification and Validation ConsultantWe are seeking a highly skilled Qualification and Validation Consultant to join our team at Groupe ProductLife. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of quality and compliance in our operations.Key Responsibilities:Manage periodic qualification and...

  • Quality Assurance Specialist

    il y a 3 semaines


    Lille, Hauts-de-France Groupe ProductLife Temps plein

    Qualification and Validation ConsultantWe are seeking a highly skilled Qualification and Validation Consultant to join our team at Groupe ProductLife. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of quality and compliance in our operations.Key Responsibilities:Manage periodic qualification and...

  • Quality Assurance Specialist

    il y a 4 semaines


    Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for clients in the life sciences industry, providing expert services in regulatory affairs, quality and compliance, vigilance, and medical information. With a global reach and local expertise, we support clients throughout the product lifecycle, from established products to...


  • Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupProductLife Group (PLG) is a life sciences consulting firm providing outsourced services in the areas of regulatory affairs, quality and compliance, vigilance and medical information. Our expertise extends to both established product monitoring and innovative therapies and diagnostics.Why Work with Us– International Company–...


  • Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupProductLife Group is a leading life sciences consulting firm providing outsourced services in the areas of regulatory affairs, quality and compliance, vigilance and medical information. Our expertise extends to both established product monitoring and innovative therapies and diagnostics.Why Work with UsWe offer a dynamic and motivated...


  • Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for life sciences companies, providing expert consulting services in regulatory affairs, quality, and compliance. With a global reach and local expertise, we support clients throughout the product lifecycle.Why Work with Us?We offer a dynamic and stimulating work environment,...


  • Lille, Hauts-de-France ProductLife Group Temps plein

    About ProductLife GroupSince 1993, ProductLife Group has been a trusted partner for life sciences companies, providing expert consulting services in regulatory affairs, quality, and compliance. With a global reach and local expertise, we support clients throughout the product lifecycle.Why Work with UsWe offer a dynamic and stimulating work environment, with...

  • Quality Assurance Specialist

    il y a 3 semaines


    Lille, Hauts-de-France Groupe ProductLife Temps plein

    Qualification and Validation Consultant (CQV) W/MWe are seeking a highly skilled Qualification and Validation Consultant (CQV) to join our team at Groupe ProductLife. As a key member of our Quality team, you will be responsible for ensuring the highest standards of quality and compliance in our operations.ResponsibilitiesManage periodic qualification and...