Remote Global Sterilization Tech Lead

SGS

Ellesmere Port

Remote

GBP 120.000 - 170.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Flexible schedule
Hybrid model
Learning platform and Campus

Zusammenfassung

SGS is seeking a Global Technical Manager – Sterilization to oversee sterilization processes for medical devices and lead the MDR Product Assessors-Sterilization team. This remote role reports to the Head of Delivery & Operations and requires deep regulatory knowledge across MDR, IVDR, and ISO13485.

You will develop training, maintain QMS docs, and ensure compliance across certification schemes while guiding a global team and supporting business growth with clients.

Qualifikationen

  • More than 10 years in the medical device industry with sterilization experience.
  • 5 years as MDR/IVDR Lead Auditor or Product Assessor – Sterilization.
  • Strong knowledge of sterilization processes, QMS and regulatory requirements.

Aufgaben

  • Oversee sterilization processes within medical devices across schemes (MDR, IVDR, ISO13485).
  • Lead the MDR Product Assessors-Sterilization team and provide technical guidance.
  • Develop and maintain sterilization training and QMS documentation.
  • Ensure regulatory compliance and support CE marking activities.
  • Drive continuous improvement and resource management within the team.

Kenntnisse

Sterilization knowledge
MDR/IVDR MDR Lead Auditor
Medical devices regulations
Team leadership
Regulatory training
Quality management systems
Problem solving
Technical documentation
Training development

Ausbildung

University or technical college degree in microbiology/related field

Jobbeschreibung

SGS is seeking a Global Technical Manager – Sterilization to oversee sterilization processes for medical devices and lead the MDR Product Assessors-Sterilization team. This remote role reports to the Head of Delivery & Operations and requires deep regulatory knowledge across MDR, IVDR, and ISO13485.

You will develop training, maintain QMS docs, and ensure compliance across certification schemes while guiding a global team and supporting business growth with clients.

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