Production Associate - LVLM (2nd, M/F, 2 - 10:30 pm)

Be part of something altogether life-changing!  

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. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.  

Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.  

The Production Associate O1 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 Large Volume Liquid Media Manufacturing department located in Logan, Utah and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. 

In this role, you will have the opportunity to: 

• 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. 

The essential requirements of the job include: 

• 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. 

• Frequently move, climb stairs and ladders daily, lift, carry, push or pull weights up to 50 lbs. unassisted and occasionally lift/move weights greater than 50 lbs. with assistance. Along with ability to wear protective equipment including clean room gowning, chemical resistant clothing, safety glasses/goggles. 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.  

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

• 2 yrs. of related manufacturing experience. 

• MS Office, Teams, Outlook, Word, and Excel. 

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