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Production Associate O1 - SVLM (2nd shift Mon-Fri 2-10:30pm)

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at Danaher Corporation in Logan, Utah, United States

Logan, UT (In Person)

Full-Time

Posted 5 days ago (Updated 3 days ago) • Actively hiring

Expires 7/2/2026

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Job Description

at Danaher Corporation in Logan, Utah, United States Job Description Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's (https://danaher.com/our-businesses) 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Production Associate has front-line responsibility in manufacturing, assembly, basic testing, packaging and shipping of products. All associates carry out the production process by closely following the standard operating procedures as they relate to materials handling, equipment operation, and finished goods packaging. This position is part of the Small Volume/Serum Manufacturing department located in Logan, Utah and will be onsite.
What you will do:
+ Ability to read and follow work policies and procedures, EHS , Quality control inspections along with schematics or receives verbal instructions regarding duties to be performed. Along with GMPs and Good documentation skills. + Complete all planned Quality & Compliance training within the defined deadlines. Identify and report any quality or compliance concerns and take immediate corrective action as required. + Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming and rework documentation requirements and operates within them to ensure that the product conforms to its specification Aware of and comply with Stop Order, Concessions, ESD , Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practi To view full details and how to apply, please login or create a Job Seeker account