Regulatory Affairs Specialist

2 weeks ago


Leeds, Leeds, United Kingdom Stelvio Group Full time £60,000 - £70,000
Job Description

Stelvio Group is seeking a highly skilled Regulatory Affairs Specialist to lead the development, management, and execution of compliance programs for our online backup and disaster recovery Managed Service Provider (MSP).

The ideal candidate will have extensive knowledge of regulatory compliance in the tech and cloud-based sectors, including data security, privacy regulations, and business continuity frameworks.

Key Responsibilities:

  • Ensure ongoing adherence to industry standards such as ISO 27001, ISO 9001, and SOC 2 Type II certifications.
  • Develop, implement, and manage policies and procedures to ensure compliance with local, regional, and international regulatory requirements.
  • Coordinate with legal, security, and operational teams to ensure appropriate safeguards are in place to meet regulatory and client-specific requirements.
  • Plan, prepare, and oversee third-party and customer audits related to compliance and certifications.
  • Maintain comprehensive documentation for all compliance activities, including policies, processes, and audit findings.

Requirements:

  • Experience with additional compliance standards, such as PCI DSS, CIS, or CSA STAR.
  • Knowledge of business continuity and disaster recovery principles.
  • Experience in implementing new compliance frameworks or standards.

What We Offer:

  • A competitive salary and benefits package.
  • The opportunity to work with a leading Managed Service Provider in the online backup and disaster recovery sector.
  • A dynamic and supportive work environment.


  • Leeds, Leeds, United Kingdom Seven Life Sciences Full time

    Job Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Seven Life Sciences. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for medical devices.Key Responsibilities:Review and update technical files for medical...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager/ConsultantWe are seeking a seasoned Senior Regulatory Affairs Manager/Consultant to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for providing expert guidance on regulatory strategies, ensuring compliance with EU guidelines, and managing client relationships.Key...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager/ConsultantWe are seeking a seasoned Senior Regulatory Affairs Manager/Consultant to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for providing expert guidance on regulatory strategies, ensuring compliance with EU guidelines, and managing client relationships.Key...


  • Leeds, Leeds, United Kingdom NHS England Full time

    Regulatory Affairs Specialist OpportunityAn exciting opportunity has arisen for a skilled Regulatory Affairs Specialist to join the patient safety team within the Transformation Directorate's Digital Clinical Informatics (DCI) team at NHS England.The role will support the quality and regulatory team in implementing and maintaining NHS-England's quality...


  • Leeds, Leeds, United Kingdom NHS England Full time

    Regulatory Affairs Specialist OpportunityAn exciting opportunity has arisen for a skilled Regulatory Affairs Specialist to join the patient safety team within the Transformation Directorate's Digital Clinical Informatics (DCI) team at NHS England.The role will support the quality and regulatory team in implementing and maintaining NHS-England's quality...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecules. This is a unique opportunity to showcase your technical skills, specialist...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecules. This is a unique opportunity to showcase your technical skills, specialist...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager/ConsultantWe are seeking a seasoned Senior Regulatory Affairs Manager/Consultant to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for providing expert guidance on regulatory strategies, ensuring compliance with EU guidelines, and managing client relationships.This is a...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager/ConsultantWe are seeking a seasoned Senior Regulatory Affairs Manager/Consultant to join our team at Lifelancer. As a key member of our regulatory affairs team, you will be responsible for providing expert guidance on regulatory strategies, ensuring compliance with EU guidelines, and managing client relationships.This is a...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecules. The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecules. The ideal candidate will possess strong regulatory affairs experience, project management skills, and in-depth...


  • Leeds, Leeds, United Kingdom William Hill Full time

    Senior Regulatory Affairs SpecialistWe are seeking an experienced professional to lead our regulatory affairs efforts. As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring that our company adheres to all relevant regulations, industry standards, and internal policies.Key Responsibilities:Oversee compliance strategies and coordinate...


  • Leeds, Leeds, United Kingdom William Hill Full time

    Senior Regulatory Affairs SpecialistWe are seeking an experienced professional to lead our regulatory affairs efforts. As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring that our company adheres to all relevant regulations, industry standards, and internal policies.Key Responsibilities:Oversee compliance strategies and coordinate...


  • Leeds, Leeds, United Kingdom Seven Life Sciences Full time

    **Job Title:** Regulatory SpecialistAt Seven Life Sciences, we are seeking a highly skilled Regulatory Specialist to join our Quality and Regulatory team. The successful candidate will be responsible for maintaining compliance with ISO 13485, Medical Device Directive 93/42/EEC, and Regulation (EU) 2017/745 (EU MDR).**Key Responsibilities:**Review, update,...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Leeds, Leeds, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...


  • Leeds, Leeds, United Kingdom Pharmiweb Full time

    Regulatory Affairs ProfessionalWe are seeking a highly skilled Regulatory Affairs Professional to join our team at Pharmiweb. As a key member of our regulatory team, you will be responsible for providing leadership in all regulatory and submissions-related aspects of clinical trials.Key Responsibilities:Provide guidance on submissions strategies and ensure...


  • Leeds, Leeds, United Kingdom Pharmiweb Full time

    Regulatory Affairs ProfessionalWe are seeking a highly skilled Regulatory Affairs Professional to join our team at Pharmiweb. As a key member of our regulatory team, you will be responsible for providing leadership in all regulatory and submissions-related aspects of clinical trials.Key Responsibilities:Provide guidance on submissions strategies and ensure...