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Guerbet is a leader in medical imaging worldwide, offering a wide range of pharmaceutical products, medical devices, digital and AI solutions for diagnostic and interventional imaging, to improve the diagnosis and treatment of patients.

A pioneer since more than 90 years in the field of contrast media, Guerbet is continuously innovating with 9% of revenue dedicated to Research & Development and four centers in France, Israel and the United States.

Guerbet (GBT) is listed on Euronext Paris (segment B – mid caps) and generated €817 million in revenue in 2019 with a global workforce of over 2,800 employees.

Achieve, Cooperate, Care and Innovate are the values that Guerbet's employees share and practice every day. Working at Guerbet means playing a unique part in the future of medical imaging. Passionate about its business, the company strive day in, day out to combine performance, quality and sustainable development.

For more information about Guerbet, please go to  and follow Guerbet on Twitter @GuerbetGroup


Production Clerk



Responsible for assisting the Process Coordinator in the assembly and completion of required documentation and data entry in support of production. 




  1. Request and update all SOP's used in production area while maintaining new effective dates & revisions
  2. Complete, fill out & assemble paperwork for each batch/lot for production area
  3. Process disposition and paperwork regarding in-process samples
  4. Perform startup checks and data entry for each production lot
  5. Complete product accountability for each batch/lot
  6. Review production start-up and in-process batch records
  7. Enter production data into BPCS manufacturing execution system
  8. Complete daily production reports & logs

9. Complete other duties as assigned by the Production Supervisor





  1. Work safely in accordance with regulations, standards, and procedures and in a manner that eliminates unreasonable risk to health and the environment.  Notify management of unsafe conditions or practices, unlawful activities and activities which present unreasonable health and/or environmental risk.  Report all safety and/or environmental incidents to management immediately.
  2. Help maintain production supplies and resources.
  3. Assist supervisor/superintendent with gathering data associated with variations.
  4. Other duties as assigned with or without accommodation.



Education required/ preferred:

High school diploma, GED, or equivalent


3-5 years pharmaceutical manufacturing experience within a sterile environment (i.e. ISO 5E or similar) preferred

Preferred Skills/Qualifications:

  • Proficient PC skills including working with spreadsheets and word processing
  • Demonstrated ability to use the Microsoft Office package


  • Working knowledge of BPCS
  • Demonstrated basic math skills
  • Good verbal and written communication skills

Other Skills:






  • Reports to Production Supervisor
  • Works daily with other operators, set-ups, mechanics and Production Supervisors.
  • Occasional interaction with cross-functional team members on project teams