Subject Matter Expert for Sterilisation Medical Products (m/f/d)

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Subject Matter Expert for Sterilisation Medical Products (m/f/d), Berlin

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Client:

Location:

Berlin, Germany

Job Category:

-

EU work permit required:

Yes

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Job Reference:

8edb702d61b3

Job Views:

1

Posted:

09.05.2025

Expiry Date:

23.06.2025

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Job Description:

Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing.

Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta.

Summary

The Flow & Fluid Sterilization specialist is responsible for all sterilization and sterilization validation activities for our disposable business. The Sterilization specialist has the technical lead of our Sterilization Board. The Sterilization specialist is also responsible for the midterm and longlterm sterilization strategy.

Primary Responsibilities

• Subject Matter Expert for Sterilization (flow & fluid) internal and external to FDA, TÜV, Customer, Sterilization Service Provider, Labs etc.
• Head of our Sterilization Board, coordinating all tasks of the Sterilization Board, creating project plans to publish the tasks of the Sterilization Board for resource balancing, allocating sufficient capacities for all sterilization tasks, doing the basic training of colleagues (System Engineers and Architects, Project Managers...)
• Member of our Standards Committee, evaluation of changes to standards, derive corresponding measures for Flow & Fluid
• Development of a midterm and longterm sterilization strategy for all NPI and series products for cost savings and EHS
• Sterilization validation for NPI products, sterilization revalidation, writing protocols, reports, adoption reports, statements and white papers. Review and release of internal and external protocols and reports.
• Routine sterilization of all series products, revalidation, evaluation of NCs, support release of serial production after sterilization
• Monitoring, qualifying, and approving process changes at sterilization service providers.
• Guarantee sufficient sterilization capacity for series production demand.
• Qualification of new sterilization service providers if required.

General Tasks

• Strict compliance with quality, occupational safety, and environmental regulations.
• Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist.

Required Experience, Education, Skills, Training and Competencies

• Several years of sterilization process experience of medical disposable products
• Knowledge of all sterilization methods and sterilization standards and guidlines
• Familiar with all relevant regulations
• Independent and interdisciplinary solution finding with more than 10 team members.
• SAP knowledge preferable

Travel Requirements

• Willingness to travel to all locations and business contacts

Physical Requirements

• Quality-conscious, trustworthy, and reliable
• Team player
• Structured and systematic way of working

#LI-UK1

#Berlin

Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.

Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.