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Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

The Associate Technician Quality Assurance Engineering of Beckman Coulter Diagnostics is responsible for full range of Instrument PM and quality control test (raw materials and in-vitro diagnostic (IVD) reagents used in clinical chemistry laboratories).

This position is part of the Quality Control Department located in Carlsbad and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Quality Control Team and report to the Quality Control Supervisor responsible for full range of Instrument PM and quality control test (raw materials and in-vitro diagnostic (IVD) reagents used in clinical chemistry laboratories). If you thrive in a high quality, strong problem solving, leadership, fast paced, supporting role and want to work to build a world-class high quality manufacturing organization—read on.

In this role, you will have the opportunity to:

• Develop knowledge and technical skills vital to assist in performing high-quality major Preventative Maintenance and troubleshooting on Beckman Coulter clinical analyzers such as DxC, Immage and AU. Support with installations, modifications, service repair requests, and be able to work independently. Engage with both internal and external stakeholders to meet onsite laboratory needs.

• Provide product lot testing in a fast-paced manufacturing environment, including raw materials, bulks and final products for clinical chemistry assays, including general chemistry and specialized tests such as therapeutic drug monitoring and drugs of abuse.

• Collaborates with other local functional groups including Manufacturing, Quality Assurance, Quality Control Test and Warehouse/Inventory Control.

The essential requirements of the job include:

• AA Degree with at least 1 year of experience in quality control or quality assurance work at a medical device (FDA/GMP) manufacturer or equivalent.

• Experience with collaborative cross-functional teams desired

• Experience with Lean tools or other continuous improvement tools desired

It would be a plus if you also possess previous experience in:

• Basic troubleshooting and problem-solving experience on clinical analyzers.

• Working with electricity that require safety protocols.

The salary range OR the hourly range for this role is 23/hr – 24/hr. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.