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Senior Systems Engineer

Thermo Fisher Scientific

Senior Systems Engineer

full-timePosted: Aug 4, 2026Updated: Sep 1, 2026Sweden, Uppsala

Job Description

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionIn this role, you will be part of Thermo Fisher Scientific's ImmunoDiagnostics Division (IDD), which develops, manufactures, and markets diagnostic tests for allergy, asthma, and autoimmune diseases.With approximately 1,900 employees worldwide, IDD is the global leader in in vitro allergy diagnostics and a leading provider of autoimmune diagnostics in Europe. Our Uppsala site, home to more than 750 employees, serves as the division's global headquarters and includes both research and development and manufacturing operations.Your future challengeWe are looking for an experienced Senior Systems Engineer to join our Sustaining Engineering & Compliance team within the R&D instrument department.In this role, you will play a key part in ensuring the long-term performance, compliance, and continuous improvement of our diagnostic products. As a technical leader, you will drive Quality Management System (QMS) development, support product lifecycle activities, and collaborate with cross-functional teams to ensure our products continue to meet customer, business, and regulatory requirements.What you will doAs a Senior Systems Engineer, you will:Lead the development, implementation, and continuous improvement of Quality Management System (QMS) processes to ensure compliance with applicable regulatory requirements.Maintain and improve technical documentation in accordance with the quality system.Provide training and system support to colleagues on quality processes and tools.Lead and contribute to sustaining engineering and product development activities.Drive process improvement initiatives to enhance product quality, efficiency, and compliance.Lead design reviews and provide technical guidance throughout development and sustaining projects.Collaborate closely with Engineering, Assay Development, Quality, Regulatory Affairs, Manufacturing, and other cross-functional teams to deliver effective technical solutions.Who are you?You are an experienced systems engineer with a passion for quality, technical leadership, and continuous improvement. You enjoy working collaboratively across functions and are motivated by solving complex engineering challenges while ensuring regulatory compliance.We believe you have:A Bachelor's degree in Engineering, Life Sciences, or a related technical field.At least five years of experience in sustaining engineering, product maintenance, quality oversight, or a similar role within the medical device, diagnostics, or another regulated industry.Strong knowledge of quality management systems and regulatory requirements for medical devices or scientific instruments.Experience leading technical initiatives and collaborating with multidisciplinary teams.Experience with Design Controls, product lifecycle management, and sustaining engineering.A structured approach with strong analytical and problem-solving skills.Experience mentoring colleagues and providing technical leadership.Excellent communication and stakeholder management skills.Fluent written and spoken English.The following are considered an advantage:An advanced degree in Engineering, Life Sciences, or a related technical field.Experience working within FDA, ISO 13485, or other regulated environments.Swedish language skills.Why join Thermo Fisher Scientific?At Thermo Fisher Scientific, your work contributes to improving patient care and advancing scientific discovery around the world. As part of our global organization, you'll collaborate with talented colleagues, lead meaningful technical initiatives, and help ensure the continued success of products that make a real difference for healthcare professionals and patients worldwide.Our Mission is to enable our customers to make the world healthier, cleaner, and safer—and our people are at the heart of making that possible.Ready for your next challenge?We look forward to receiving your application.Apply today!Applications will be reviewed after the summer holiday period in August. The position will be filled as soon as a suitable candidate has been identified, so we encourage you to submit your application as early as possible.

Locations

  • Sweden, Uppsala

Skills Required

  • sustaining engineeringintermediate
  • quality management systemsintermediate
  • Design Controlsintermediate

Required Qualifications

  • A Bachelor's degree in Engineering, Life Sciences, or a related technical field. (degree in engineering)
  • At least five years of experience in sustaining engineering, product maintenance, quality oversight, or a similar role within the medical device, diagnostics, or another regulated industry. (experience)
  • Strong knowledge of quality management systems and regulatory requirements for medical devices or scientific instruments. (experience)
  • Experience leading technical initiatives and collaborating with multidisciplinary teams. (experience)
  • Experience with Design Controls, product lifecycle management, and sustaining engineering. (experience)
  • A structured approach with strong analytical and problem-solving skills. (experience)
  • Experience mentoring colleagues and providing technical leadership. (experience)
  • Excellent communication and stakeholder management skills. (experience)
  • Fluent written and spoken English. (experience)

Responsibilities

  • Lead the development, implementation, and continuous improvement of Quality Management System (QMS) processes to ensure compliance with applicable regulatory requirements.
  • Maintain and improve technical documentation in accordance with the quality system.
  • Provide training and system support to colleagues on quality processes and tools.
  • Lead and contribute to sustaining engineering and product development activities.
  • Drive process improvement initiatives to enhance product quality, efficiency, and compliance.
  • Lead design reviews and provide technical guidance throughout development and sustaining projects.
  • Collaborate closely with Engineering, Assay Development, Quality, Regulatory Affairs, Manufacturing, and other cross-functional teams to deliver effective technical solutions.

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