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Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
Production Specialist 1 - Documentation (LVLM, 2nd shift) in Logan, UT
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Production Specialist 1 - Documentation (LVLM, 2nd shift)
Company: Cytiva
Location: Logan, UT
Employment Type: Full Time
Date Posted: 11/26/2020
Expire Date: 01/30/2021
Job Categories: Arts, Entertainment, and Media, Biotechnology and Pharmaceutical, Engineering, Healthcare, Other, Information Technology, Internet/E-Commerce, Manufacturing and Production, Executive Management, Quality Control, Research & Development, Web Technology, Writing/Authoring
Job Description
Production Specialist 1 - Documentation (LVLM, 2nd shift)

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

What youll do

  • The Production Specialist may have responsibilities including manufacturing, assembly, basic testing, packaging, and shipping of products. In addition, the production specialist is responsible to have specialized knowledge, skills, and abilities relating to the production process and procedures.
  • Follows work procedures and schematics including complex instructions regarding duties to be performed
  • Performs manufacturing/assembly operations and various tasks following procedures, bills of materials, work instructions, and process aid sheets
  • Assists in the writing and/or developing of work procedures
  • Works independently and completes basic troubleshooting
  • Maintains daily production output numbers
  • Assists in shift startup and delegatory responsibilities in absence of team leader
  • Participates in quality control inspections when required
  • Works with team leaders, engineers, supervisors, and managers to improve quality and process efficiency
  • Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
  • Performing more advanced and complex assembly and testing when required
  • Trains other team members when required
  • Comply with EHS regulations and policies


  • Demonstrate ability to design and perform 1L benchtop and use data for investigation purposes
  • Understand and explain 8D concept
  • Demonstrate ability to lead and participate in 8D investigation process
  • Demonstrate ability to participate in spec development process
  • Explain the components to look for during spec development
  • Participate in chemical hazard review process
  • Understand investigative resources and tools
  • Participate in data collection process for investigations
  • Assist with work-order process for LM formulation equipment
  • Understand product definitions and basic chemistry of components
  • Demonstrate ability to revise WID and participate in collaboration process
  • Successfully complete NOE, Corrective Task, and Temp Change
  • Demonstrate ability to troubleshoot all formulations / issues

Quality Specific Goals

  • Aware of and comply with the Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
  • 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
  • Ensures the creation of accurate, complete and timely records 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
  • One year of similar operations experience
  • Ability to communicate, receive and understand instructions regarding duties to be performed
  • Demonstrated ability to detail and quality-minded work habits
  • Demonstrated ability to communicate with co-workers and leadership

Physical Requirements

  • Frequently move, lift, carry, push or pull weights up to 50 pounds unassisted and occasionally lift/move weight greater than 50 pounds with assistance
  • Frequently climb stairs and ladders
  • Frequently squat, stoop, kneel, crouch, turn, pivot and reach
  • Frequently use fingers or hands to grasp, clamp, move, finger, handle and feel small objects
  • Ability to continuously stand or walk
  • Ability to wear protective equipment including clean room gowning, chemical resistant clothing, safety glasses/goggles
  • Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust and focus on objects

Desired Characteristics

  • Associates or technical degree
  • 1-2 years media production experience preferred

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, youll feel right at home here. If youre flexible, curious and relentless, youll belong. If you are excited about a global culture, this can be the place to further your career.

Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!

Cytiva is a 3.3 billion USD global life sciences leader with nearly 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.

Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The EEO is the Law poster is available here.

Contact Information
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Company Name: Cytiva
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Website: https://jobs.danaher.com/global/en/...
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