Cleaning Validation Technician / Quality Engineer

Job Opening for Cleaning Validation Technician / Quality Engineer, Augusta, GA

Duties: Cleaning Validation Technician / Quality Engineer

LOA: 12 mo

Augusta, GA

What Manufacturing Engineering contributes to Cardinal Health
Manufacturing Engineering is responsible for developing manufacturing processes, production floor layouts and associated tools. Reviews new designs for manufacturability. Designs process improvements to reduce product cost, process cycle time and improved product quality
Accountabilities:

Responsible for technical support and life-cycle management of the cleaning validation program
Maintains a qualified state of cleaning processes and procedures, as well as designing and implementing new cleaning processes.
Maintains the site cleaning validation master plan
Conducts risk assessments of existing and new processes, equipment, etc. as it relates to cleaning procedures/validation
Designs and executes cleaning process optimization studies, cleaning verification and cleaning validation studies
Manages, schedules, coordinates, and executes cleaning engineering studies to optimize cleaning procedures, cleaning verification studies, and cleaning validation studies
Designs and develops equipment cleaning procedures
Prepares and executes cleaning protocols and reports for cleaning development and validation
Investigates cleaning failures
Supports the periodic review of cleaning validation studies
Develops change controls for implementation of cleaning procedure changes as needed
Trains manufacturing and QC personnel on cleaning validation protocols and procedures
Follows all certified standards, GMP, OSHA, plant policies and procedures

A COVID-19 vaccination is required in order to be employed in this position. This includes either:

2 doses of the Moderna or Pfizer vaccine
1 dose of the Johnson & Johnson vaccine

Fully vaccinated means that two weeks have passed since the last required dose of the COVID vaccine. Contractors may not begin their assignment until fully vaccinated.

Skills: What is expected of you and others at this level

Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
May contribute to the development of policies and procedures
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives
Completes work independently receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues

Job Opening for Cleaning Validation Technician / Quality Engineer, Augusta, GA

Duties: Cleaning Validation Technician / Quality Engineer

LOA: 12 mo

Augusta, GA

What Manufacturing Engineering contributes to Cardinal Health
Manufacturing Engineering is responsible for developing manufacturing processes, production floor layouts and associated tools. Reviews new designs for manufacturability. Designs process improvements to reduce product cost, process cycle time and improved product quality
Accountabilities:

Responsible for technical support and life-cycle management of the cleaning validation program
Maintains a qualified state of cleaning processes and procedures, as well as designing and implementing new cleaning processes.
Maintains the site cleaning validation master plan
Conducts risk assessments of existing and new processes, equipment, etc. as it relates to cleaning procedures/validation
Designs and executes cleaning process optimization studies, cleaning verification and cleaning validation studies
Manages, schedules, coordinates, and executes cleaning engineering studies to optimize cleaning procedures, cleaning verification studies, and cleaning validation studies
Designs and develops equipment cleaning procedures
Prepares and executes cleaning protocols and reports for cleaning development and validation
Investigates cleaning failures
Supports the periodic review of cleaning validation studies
Develops change controls for implementation of cleaning procedure changes as needed
Trains manufacturing and QC personnel on cleaning validation protocols and procedures
Follows all certified standards, GMP, OSHA, plant policies and procedures

A COVID-19 vaccination is required in order to be employed in this position. This includes either:

2 doses of the Moderna or Pfizer vaccine
1 dose of the Johnson & Johnson vaccine

Fully vaccinated means that two weeks have passed since the last required dose of the COVID vaccine. Contractors may not begin their assignment until fully vaccinated.

Skills: What is expected of you and others at this level

Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
May contribute to the development of policies and procedures
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives
Completes work independently receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues