Current jobs related to Regulatory Compliance Specialist - Bedford - Wells & Co Careers

  • Regulatory Affairs Specialist

    4 days ago

    Bedford, Bedford, United Kingdom Werfen Full time

    OverviewWerfen, a global leader in diagnostic instruments, seeks a highly skilled Regulatory Affairs Specialist to join our team. This role will focus on ensuring compliance with regulatory requirements for our medical devices in international markets.Key ResponsibilitiesDevelop and implement regulatory strategies to satisfy NMPA and PMDA...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Regulatory Affairs team at Werfen, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Regulatory Affairs team at Werfen, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full time

    Job Title: Regulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging, with a strong commitment to innovation and patient care. We are seeking an experienced Regulatory Affairs Specialist to join our team.About the RoleWe are looking for a highly skilled and motivated individual to lead the development and...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full time

    Job Title: Regulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging, with a strong commitment to innovation and patient care. We are seeking an experienced Regulatory Affairs Specialist to join our team.About the RoleWe are looking for a highly skilled and motivated individual to lead the development and...

  • Regulatory Affairs Specialist

    1 month ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role involves developing and implementing regulatory strategies, preparing regulatory plans and submissions, and collaborating with cross-functional teams to ensure regulatory compliance.Key...

  • Regulatory Affairs Specialist

    1 month ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role involves developing and implementing regulatory strategies, preparing regulatory plans and submissions, and collaborating with cross-functional teams to ensure regulatory compliance.Key...

  • Senior Regulatory Affairs Specialist

    5 months ago

    Bedford, United Kingdom SPD Development Company Ltd Full time

    **Senior Regulatory Affairs Specialist** Swiss Precision Diagnostics (SPD) is a world leader in the research, design and supply of advanced consumer diagnostic products. SPD is a joint venture between **Procter & Gamble (P&G)** and **Abbott**; and our brand **Clearblue**, is recognised the world over as providing accurate home pregnancy and fertility...

  • Regulatory Affairs Specialist

    1 month ago

    Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full time

    Regulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging, with a strong commitment to innovation and patient care. We are seeking an experienced Regulatory Affairs Specialist to join our team.Key Responsibilities:Develop and implement regulatory strategies for advertising and promotional materials,...

  • Regulatory Affairs Specialist

    1 month ago

    Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full time

    Regulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging, with a strong commitment to innovation and patient care. We are seeking an experienced Regulatory Affairs Specialist to join our team.Key Responsibilities:Develop and implement regulatory strategies for advertising and promotional materials,...

  • Regulatory Affairs Specialist

    2 weeks ago

    Bedford, Bedford, United Kingdom Lantheus Medical Imaging Inc Full time

    Regulatory Affairs SpecialistLantheus Medical Imaging Inc is a leading company in the field of medical imaging. We are seeking an experienced Regulatory Affairs Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs, with a focus on labeling and promotional communications. The successful candidate will be...

  • Regulatory Affairs Specialist

    4 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    4 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    3 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job SummaryThe Principal Regulatory Specialist is a key member of the Werfen team, responsible for ensuring compliance with regulatory requirements for medical devices and in vitro diagnostics. This role requires a strong understanding of FDA, MDSAP, IVDR, MDR, and international regulations, as well as ISO and other international...

  • Regulatory Affairs Specialist

    7 days ago

    Bedford, Bedford, United Kingdom Werfen Full time

    OverviewWerfenWerfen is a global leader in the development, manufacturing, and distribution of specialized diagnostic instruments, reagents, and data management solutions for hospitals and clinical laboratories. Our business lines include Hemostasis, Acute Care, and Autoimmunity diagnostics, as well as Original Equipment Manufacturing. We prioritize...

  • Regulatory Affairs Specialist

    2 weeks ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job Summary:Werfen is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for our medical devices in China and Japan.Key Responsibilities:Participate in design and risk management teams to provide guidance on regulatory...

  • Regulatory Affairs Specialist

    2 days ago

    Bedford, Bedford, United Kingdom Werfen Full time

    OverviewWerfenWerfen is a global leader in the development, manufacturing, and distribution of specialized diagnostic instruments, reagents, and data management solutions. With a strong focus on innovation and quality, we provide healthcare professionals with valuable and complete solutions to improve hospital efficiency and enhance patient care. Our...

  • Senior Regulatory Affairs Specialist

    2 months ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Werfen. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for medical devices in China and Japan.Key Responsibilities:Participate in design and risk management teams to provide guidance on regulatory...

  • Senior Regulatory Affairs Specialist

    2 months ago

    Bedford, Bedford, United Kingdom Werfen Full time

    Job Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Werfen. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for medical devices in China and Japan.Key Responsibilities:Participate in design and risk management teams to provide guidance on regulatory...

Regulatory Compliance Specialist

2 months ago

Bedford, United Kingdom Wells & Co Careers Full time
Compliance Coordinator - Wells & Co
We are looking for a detail-oriented and proactive Compliance Coordinator to support our legal team. This role is perfect for individuals who excel in dynamic environments and possess strong organizational skills.

Key Responsibilities:
  • Oversee the organization and management of legal documentation.
  • Assist in coordinating health and safety initiatives, projects, and data management.
  • Conduct policy assessments and compliance evaluations to ensure adherence to legal standards and internal guidelines.
  • Manage trademark processes and monitor potential conflicts.
  • Gather customer due diligence data to evaluate financial risks.
  • Facilitate licensing modifications and renewals in compliance with regulations.
  • Conduct training sessions for managers on licensing and compliance protocols.
  • Organize licensing workshops to ensure compliance with personal licensing requirements.
  • Handle insurance claims and investigations, ensuring timely data submission to insurers.
  • Coordinate the registration and updating of company records with relevant authorities.
  • Manage company share and bond documentation and pension scheme records.
  • Assist in preparing materials for board meetings.
  • Support the planning of meetings and events, ensuring accurate record-keeping.
  • Maintain the integrity of data within the company’s information systems in accordance with data protection regulations.
  • Oversee the processing of invoices related to legal services.
Experience Required:
  • Exceptional organizational and communication abilities, with a strong attention to detail.
  • Proficient in IT applications including Excel, Word, PowerPoint, and Microsoft Teams.
  • Self-motivated and capable of working independently as well as collaboratively.
  • Strong prioritization skills with the ability to manage multiple tasks effectively.
  • Ability to analyze and interpret complex compliance-related information.