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Thermo Fisher Scientific

Thermo Fisher Scientific

Lab supplies, instruments, and biopharma services

Manager, Refrigeration Engineering - ULT

Full-Time
No salary listed
Senior
Bachelor's, Master's
Marietta, OH, USA+4 more

More locations: Cleveland, OH, USA | Pittsburgh, PA, USA | Columbus, OH, USA | Cincinnati, OH, USA

In Person

This is a fully onsite role in Marietta, Ohio, with up to 10% domestic travel.

About the job

Requirements
  • A bachelor's degree in mechanical engineering, systems engineering, chemical engineering, physics, or a related discipline is required.
  • At least 5 years of experience leading teams in the design and evaluation of refrigeration or thermal systems is required.
  • At least 3 years of hands-on experience developing vapor-compression systems for cold storage or HVAC/R products is required; cascade systems experience is preferred.
  • Experience using natural refrigerants and other low-global-warming-potential refrigerants in system designs is required.
  • Experience supporting regulated products, including UL 61010, ISO 13485, ISO 14971, FDA, CE, CSA, or Energy Star requirements, is required.
  • Experience with thermal system modeling, simulation, and performance testing is required.
  • Experience analyzing empirical test data to guide design decisions is required.
  • Familiarity with data acquisition systems, automated testing, and technical documentation is required.
  • Familiarity with Lean, PPI methodologies, and continuous improvement systems is required.
  • Strong knowledge of vapor-compression and cascade refrigeration systems is required.
  • Expertise in thermal modeling, simulation, and performance optimization is required.
  • Strong analytical, problem-solving, and root-cause analysis skills are required.
  • Experience using engineering tools such as EES, thermal modeling software, and Microsoft Office is required.
  • The ability to translate complex technical concepts into actionable business decisions is required.
  • Strong leadership, communication, and cross-functional collaboration skills are required.
  • Excellent organizational skills in a fast-paced, multi-project environment are required.
  • A commitment to safety, quality, and operational excellence is required.
Responsibilities
  • Lead and manage a global refrigeration engineering organization responsible for cascade vapor-compression systems used in ultra-low-temperature freezers and cold storage platforms.
  • Own refrigeration system architecture and strategy aligned with product roadmaps and platform reuse initiatives.
  • Provide technical oversight for sealed-system design, including compressors, heat exchangers, refrigerants, controls interfaces, and safety devices.
  • Drive modular, scalable, and reusable refrigeration solutions across multiple product platforms.
  • Lead thermal modeling, system simulation, and analytical work to predict performance, efficiency, and reliability.
  • Guide design trade studies using modeling and empirical data to optimize system performance and energy consumption.
  • Champion advanced development initiatives to mature next-generation refrigeration technologies and support intellectual property creation.
  • Collaborate with mechanical, electrical, and controls engineering teams through all phases of the toll-gate new product development process.
  • Partner with manufacturing and operations teams to ensure robust design transfer and global production readiness.
  • Support products manufactured across multiple global facilities.
  • Contribute to component, subsystem, and system-level technology roadmaps.
  • Partner with Product Management, Controls Engineering, Quality, and Regulatory to develop and maintain refrigeration and control requirements.
  • Ensure traceability from customer and regulatory requirements through verification and validation evidence.
  • Ensure refrigeration designs meet applicable regulatory and certification requirements, including UL, IEC, FDA, CE, CSA, and Energy Star.
  • Drive standardization of system-level specifications, test plans, and validation methods.
  • Develop budgets, resource plans, and schedules in partnership with new product development project managers and leadership.
  • Balance internal resources, global engineering contractors, and third-party support.
  • Coach, mentor, and develop engineers and technicians to build technical capability and leadership depth.
  • Foster a culture of safety, quality, accountability, and continuous improvement.
  • Travel up to 10% domestically.
Desired Qualifications
  • Coursework in thermodynamics, heat transfer, and fluid mechanics is strongly preferred.
  • A master's degree is preferred.
  • Experience developing cascade vapor-compression systems is preferred.

About the company

Thermo Fisher Scientific

Thermo Fisher Scientific

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Thermo Fisher Scientific supplies labs, hospitals, and biotech firms with a broad range of products and services, from basic lab consumables to advanced analytical instruments and outsourced drug development. Its offerings work by combining high-tech instruments for genomics, diagnostics, and research with consumables and a global distribution network to deliver end-to-end workflows that turn samples into data and insights. The company differentiates itself through its massive, diversified portfolio and its integrated end-to-end reach—from tools and reagents to support services—built on the legacy of Fisher Scientific’s distribution strength and Thermo Electron’s instrument innovation, backed by a history of strategic acquisitions. The goal is to be the dominant partner in science and healthcare by enabling researchers and clinicians to perform work more efficiently and at larger scale, spanning discovery, development, and manufacturing.

Company Size

10,001+

Company Stage

IPO

Headquarters

Waltham, Massachusetts

Founded

1956

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Simplify's Take

What believers are saying

  • Second-quarter 2026 revenue rose 10.5% to $11.99 billion, and EPS beat estimates.
  • Management raised 2026 organic growth to about 4% after stronger second-half orders.
  • September 2026 launches—Orbitrap Isora, EMPAD G2, and Heratherm chambers—expand premium workflow sales.

What critics are saying

  • Clario integration and microbiology divestiture distract management through 2027.
  • Bruker, Waters, and Agilent attack Thermo Fisher's high-margin mass-spec and chromatography franchises.
  • Biopharma funding freezes and NIH grant cuts hit orders fast; prolonged weakness threatens growth.

What makes Thermo Fisher Scientific unique

  • Thermo Fisher spans consumables, instruments, diagnostics, and PPD services across every lab workflow.
  • Orbitrap, Olink, and proprietary automation integrate discovery, analysis, and outsourced development.
  • Mayo Clinic Precure and KAIST SHARE Hub deepen data, AI, and automation moats.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Unlimited Paid Time Off

Paid Vacation

Paid Sick Leave

Paid Holidays

Hybrid Work Options

401(k) Retirement Plan

401(k) Company Match

Employee Stock Purchase Plan

Fertility Treatment Support

Family Planning Benefits

Professional Development Budget

Conference Attendance Budget

Wellness Program

Mental Health Support

Gym Membership

Phone/Internet Stipend

Home Office Stipend

Company News

PR Newswire
Sep 15th, 2026
Mayo Clinic and Thermo Fisher launch Precure to detect disease before symptoms appear

Mayo Clinic and Thermo Fisher Scientific have launched Precure, LLC to identify early biological signs of disease before symptoms appear. Mayo Clinic will be the majority owner, with Thermo Fisher as a minority partner. The venture will create one of the world's largest biomedical datasets by generating multi-omics data from one million biospecimens. It will integrate proteomic, genomic and longitudinal clinical data to help researchers identify early disease signals across conditions including cancer, cardiometabolic disease, neurological disorders and immune-mediated diseases. Mayo Clinic will contribute clinical expertise, biospecimens and de-identified patient data. Thermo Fisher will provide proteomics technology, including its Olink Explore HT platform and Orbitrap Mass Spectrometry systems. The initiative will use advanced AI and data analytics to identify patterns and translate findings into actionable insights.

BioSpectrum Asia
Sep 15th, 2026
Thermo Fisher introduces small-format, stackable environmental chambers ideal for quality control and safety testing.

Thermo Fisher introduces small-format, stackable environmental chambers ideal for quality control and safety testing. September 15, 2026 | Tuesday | News For pharmaceutical and biotech labs conducting drug stability testing or cell culture research. US-based Thermo Fisher Scientific has introduced the Thermo Scientific (TM) Heratherm(TM) Environmental Chambers with a 250-liter capacity, offering precise control to simulate several climate conditions. These small-format, stackable environmental chambers complement Thermo Fisher 's 750-liter capacity Heratherm Environmental Chambers to provide labs of all sizes the precision needed for stability testing, sample storage and quality control applications. Ideal for highly regulated environments, the Heratherm Environmental Chambers offer a programmable interface, including restricted user modes, remote monitoring capabilities and sophisticated data logging to support 21 CFR Part 11 data management and traceability. They also offer at-a-glance sample status for more efficient monitoring. The Heratherm Environmental Chambers are available in three stackable, small-format models: Heratherm Stability Chamber, Heratherm CO2 Chambers and Heratherm Incubation Chambers, which feature flexible configurations to fit the needs of various labs, including simultaneous testing and long-term studies.

Chemistry World
Sep 3rd, 2026
Antibody data manipulation extends to thousands of images across 15 suppliers.

Antibody data manipulation extends to thousands of images across 15 suppliers. After identifying antibody validation data manipulation in Thermo Fisher Scientific's catalogue in May, the science sleuths and researchers behind the finding have now uncovered doctored validation data on a much larger scale, with over 18,000 images relating to over 17,000 antibodies from at least 15 different supplier companies. Reese Richardson, Elisabeth Bik and Sholto David - who spotted the first doctored blot - have led the investigation. Community reports have also come in from across the world, with the annotated images continuing to be collated in an online repository. The team has traced some suspected image manipulation back over a decade ago. The team has uncovered various forms of image manipulation - this example from Abcam includes areas of background that have been duplicated The companies identified span major suppliers as well as more specialist firms, including MilliporeSigma, G-Biosciences, Proteogenix, Abcam and Origene. Western blots - which show how an antibody binds to a given protein - and other validation images have been identified as manipulated, calling into question not just transparency but antibody performance. This includes 'painting' of immunofluorescence images used to visualise the distribution or localisation in cells. I think that everybody should be demanding change. It's a massive insult from for-profit companies to the research community. Reese Richardson Image integrity expert Bik says Western blot manipulation is easier to uncover, but immunofluorescence manipulation takes more digging. With increasing use of artificial intelligence (AI), identifying doctored images is becoming more difficult. While she wasn't surprised to discover image manipulation from more companies, Bik says the extent is 'shocking' to see. 'I'm very worried about AI,' she adds. 'It may be already happening that images are AI-generated, and how will we detect that?' Until now, she suggests, there has been a level of trust and expectation of quality - given the high prices of antibody reagents. When experiments fail, or results are not as clean as expected, researchers tend to attribute that to their own errors, rather than ineffective reagents. Bik says the impact on research is unmeasurable but 'it must be millions or billions in wasted research funding'. It also raises ethical questions for researchers who use these antibodies as part of animal studies. Bik adds there must be 'some degree of regulation' introduced. Richardson says the contributions and support from scientists gives him hope for change: 'I think that everybody should be demanding change. It's an immense waste of [researchers'] time [and resources] that people have been buying antibodies based off fabricated data. It's a massive insult from for-profit companies to the research community. What we need now is transparency.' The teams have found hundreds of images in which protein binding bands appear to have been pasted onto the same background image. Some background patterns are present across images from multiple different companies Following the pattern Richardson explains that with image background patterns being replicated for antibodies across different companies, it's likely for many that 'no experiment took place'. He adds that many companies are buying antibodies from the same manufacturer, then selling them under their own brands at different prices (and with different quality guarantees) without clearly disclosing the source. However, some companies' validation data show 'unique styles' of image manipulation - like Proteogenix and Santa Cruz Biotechnology - with individual patterns reused extensively within their own antibody catalogues. This leads Richardson to suspect 'fudging the validation data' may be common practice across the industry. The companies with the largest number of doctored images are G-Biosciences and Thermo, each with more than 5000 images identified, and LSBio and Origene with more than 2000 images each. However, without running a complete audit of all the companies' catalogues, the full extent of the problem remains unclear. Thermo and Abcam have begun their own internal reviews. Thermo says it has so far found 'no evidence of impact to antibody performance' and is updating and replacing some Western blot images, as well as adding labelling to distinguish raw, unedited images from those that may have been 'edited, optimised or adjusted'. Tracing the changes Richardson explains that forensic image analysis tools can reveal metadata showing when images were opened in Photoshop and other editing software. With this, science sleuths tracked some of the alterations made over time. However, he is clear that this alone is 'not a smoking gun', since Photoshop can be used to make legitimate changes such as cropping and adding labels. The incriminating evidence, he says, is traces of multiple modifications that go beyond what would be required for simple labelling. Another example of repeated use of the same background pattern to create multiple images, this time all taken from Proteogenix's catalogue This includes some images first logged as far back as 2011: 'Many don't just preserve the first time an image was created and when it was last modified, but session data for every modification made along the way,' he explains. Taking the images that share one specific background pattern, for instance, the team can reconstruct an evolutionary tree from the original image, showing every time it was modified thereafter. Modifications have unique session identifiers but do not show how the image was altered. 'You can see if the first 20 session IDs match the whole 20 of a different image, so you can see where an image was branched off and manipulated from the same template,' he says. One example has up to 80 different session IDs, suggesting modification goes far beyond acceptable changes for presentation. I hope there will be some lawsuit, I'm not a fan of suing people in general but this is a big scandal Elisabeth Bik While the original data is needed for a clearer picture, the thousands of images identified so far represents the proportion uncovered after hours of work from the science sleuths - often alongside other work. Bik says there's little individual scientists can do, but companies should now be checking their supply chains, identifying fault and taking responsibility. However, she has 'little hope' change will come soon. 'I don't know how they'll rebuild trust. I hope there will be some lawsuit, I'm not a fan of suing people in general but this is a big scandal.' Few scientists will feel they have the time or means for such a lawsuit, however, and pressure to keep producing results means they are unlikely to boycott major antibody suppliers. She suggests that research funders like the US National Institutes of Health could potentially pursue lawsuits for wasted funding, but most likely, she suggests 'nothing will happen'. Richardson sees this as a 'cautionary tale' of the privatisation of essential research services in general and specifically the for-profit model of antibody production. Independent organisation YCharOS validating antibodies with gold standard protocols estimates these tests can cost up to $25,000 per reagent. He says this cost, combined with the lack of regulatory oversight, provides an incentive to either modify or fabricate validation data. He agrees with Bik that regulation is necessary. In the meantime, Richardson says researchers should run their own validation, since 'clearly, we cannot count on the industry to do it for us'. Frankie Macpherson is digital content assistant working with the wider Chemistry World team to help create and publish articles, social media content, podcasts and deliver events. View full profile

Zenopa
Sep 2nd, 2026
Thermo Fisher Launches Multiskan Ease Microplate Reader

Thermo Fisher Launches Multiskan Ease Microplate Reader 2nd September 2026 We have hundreds of jobs available across the Healthcare industry, find your perfect one now. Receive the latest industry news, Tips and straight to your inbox.

Associated Press
Sep 2nd, 2026
Thermo Fisher launches Multiskan Ease microplate reader for protein and cell analysis

Thermo Fisher Scientific has launched the Multiskan Ease Absorbance Microplate Reader, designed to simplify protein quantification, enzyme-linked immunosorbent assays, cell viability studies and microbial growth monitoring in laboratories. The device was developed for laboratories facing budget constraints, shared resources and workforce challenges that need a straightforward absorbance solution for routine biological assays. It supports applications including protein quantification, ELISAs, enzyme activity analysis, endotoxin testing and microbial growth monitoring. "The Multiskan Ease was developed to provide the performance researchers need for routine biological analysis in a platform that is easy to adopt, straightforward to operate and designed to support laboratory productivity," said Trent Colville, senior director and general manager of protein detection and quantification at Thermo Fisher Scientific. The system targets academic, biotechnology, pharmaceutical and quality control laboratories.