Production Associate O1 (2nd shift, SVLM/Serum, M-F, 2-10:30 pm)

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 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 which makes everything possible..

The Production Associate O1 for Cytiva is responsible for production and ensuring the day-to-day work task are completed in an ethical, safe manner.

This position is part of the Small Volume Liquid Media/Serum Manufacturing department located in Logan, UT and will be an onsite position. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

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 Practices, as associated with this job type/position.

Who you are:

• High School Diploma/GED or local equivalent

• Ability to work well and communicate with team lead, engineers, supervisors, and managers to improve quality and process efficiency.

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Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to frequently move, climb stairs and ladders daily, lift, carry, push or pull weight up to 50 lbs. Occasionally lift/move weights greater than 50 lbs. with assistance.

• Frequently squat, stoop, kneel, crouch, turn, pivot and reach.

• Frequently use fingers or hands to grasp, clamp, move, finger, handle and feel small objects. 

• Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust and focus on objects.

• Along with ability to adhere to the ISO5 environment and wear PPE including clean room gowning, chemical resistant clothing, safety glasses/goggles.

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

• Manufacturing or production experience

• MS Office programs

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our prog