Sterilization Experts

vor 1 Woche


Hamburg, Hamburg, Deutschland DNV Vollzeit

Local Unit & Position Description:

Objective of the role:


MEDCERT is an accredited Certification Body for ISO 13485, recognised auditing organization under MDSAP and approved Notified Body for Medical Devices Regulation.

We provide global market access by certifying the safety and quality of products and systems to international safety and quality standards and regulations.

Our high professional standards and our sustainable approach guarantee you a forward-thinking work environment, within an organisation that invests in its employees, and is committed to providing you with continued development.


Medical Devices - Product Assurance
The production of medical devices is a strictly regulated business. MEDCERT is a Notified Body, providing services that secure our customers' market access around the world. We assist the industry in ensuring medical devices are safe, effective and of the highest standard and quality.

Position Qualifications:

  • Successfully completed course of study of medicine, natural sciences or engineering science at a university or technical college ("Fachhochschule"). Only in special cases which have to be justified and comprehensible equivalent knowledges and skills.
  • Sufficient knowledge and experience in the areas directly related to the production of sterile products
  • 4 years of professional experience including at least 2 years of employment in the areas directly related to the production technology and/or sterilization technology to be assessed or equivalent experience with general process technology
  • Appropriate provable Knowledge of the European and national medical device regulation.
  • Experience and/or training in cleanroom technology, determination of bioburden, validation of cleaning, disinfection, and sterilization procedures, sterile packaging
  • Proof of successful participation in at least one course of study on validation of sterilization with ethylene oxide and/or radiation and/or steam in accordance with EN 11135, EN 11137 EN 17665 and the requirements for medical products to be labelled as sterile, or equivalent qualification
  • Basic knowledge in the area of hygiene
  • Knowledge of staff hygiene, environmental monitoring, determination of EO or other residuals
  • Fluent in English, both spoken and written

Competency Requirements:

  • Structured, able to take initiative and work independently as well as part of a team
  • Good communication skills and customer focus
  • Ability to cope with a dynamic and changing environment
  • Strong software skills (Microsoft Office)
  • Cross cultural collaboration

Company & Business Area Description:
DNV is the independent expert in assurance and risk management, operating in more than 100 countries.

Through our broad experience and deep expertise we advance safety and sustainable performance, set industry benchmarks, and inspire and invent solutions.

We are one of the world's leading certification, assurance and risk management providers.

Whether certifying a company's management system or products, providing training, or assessing supply chains, and digital assets, we enable customers and stakeholders to make critical decisions with confidence.

We are committed to support our customers to transition and realize their long-term strategic goals sustainably, and collectively contributing to the UN Sustainable Development Goals.


Equal Opportunity Statement:


DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender, religion, race, national or ethnic origin, cultural background, social group, disability, sexual orientation, gender identity, marital status, age or political opinion.

Diversity is fundamental to our culture and we invite you to be part of this diversity

  • Hamburg, Hamburg, Deutschland Olympus Vollzeit

    Ihre Aufgaben -Serve as a primary consultant and resource person regarding infection prevention (IP) issues in the area of complaint handling resolution -Take a lead in reviewing and analyzing patient infection and endoscope contamination incidents, contributes to the root cause analysis as well as to the identification of relevant mitigating actions...

  • Technical Expert

    vor 3 Wochen


    Hamburg, Deutschland Olympus Europa SE & Co. KG (OEKG) Vollzeit

    **Responsibilities**: - Provide technical 2nd level support for our CDS (Cleaning/Disinfection/Sterilization) products by phone, augmented reality or our EMEA-wide remote support environment - If required, escalate inquiries to the 3rd level support at OSTE (Olympus Surgical Technologies Europe) - Perform on-site technical support at customer site upon...

  • Technical Expert

    vor 4 Wochen


    Hamburg, Deutschland Olympus Europa SE & Co. KG (OEKG) Vollzeit

    **Responsibilities**: - Provide technical 2nd level support for our CDS (Cleaning/Disinfection/Sterilization) products by phone, augmented reality or our EMEA-wide remote support environment - If required, escalate inquiries to the 3rd level support at OSTE (Olympus Surgical Technologies Europe) - Perform on-site technical support at customer site upon...


  • Hamburg, Deutschland Olympus Vollzeit

    Ihre Aufgaben -Serve as a primary consultant and resource person regarding infection prevention (IP) issues in the area of complaint handling resolution -Take a lead in reviewing and analyzing patient infection and endoscope contamination incidents, contributes to the root cause analysis as well as to the identification of relevant mitigating actions...


  • Hamburg, Deutschland Olympus Vollzeit

    Ihre Aufgaben -Serve as a primary consultant and resource person regarding infection prevention (IP) issues in the area of complaint handling resolution -Take a lead in reviewing and analyzing patient infection and endoscope contamination incidents, contributes to the root cause analysis as well as to the identification of relevant mitigating actions...


  • Hamburg, Deutschland Olympus Vollzeit

    Ihre Aufgaben -Provide deep expertise, insights, as well as scientific and clinical leadership to IP strategy and strategic decision making while maintaining a sharp focus on patient safety throughout the product lifecycle, including new product development processes, R&D engineering, risk management, clinical trials, post-market safety surveillance,...