Cleanroom Compliance & Process Improvement Technician

Fagron Sterile Services US (FSS); Wichita (KS); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Job summary

Fagron US is seeking a Cleanroom Specialist to support sterile manufacturing by reviewing batch records for cGMP compliance, updating SOPs, and assisting with process improvements and production scheduling.

The role also manages cleanroom logbooks, supports document retention, and helps maintain inventory accuracy. Candidates should have at least two years of cleanroom manufacturing experience and strong attention to detail.

Qualifications

• At least 2 years of manufacturing experience within the cleanroom.
• Ability to communicate effectively.
• Attention to detail with a low number of errors on record.
• Knowledge of CGMP regulations and practices.
• Ability to take initiative and work independently; strong prioritization and multitasking.

Responsibilities

• Performs a review of batch records for cGMP compliance.
• Assist with process improvements including change control management.
• Updates Standard Operating Procedures.
• Assist with production schedule creation.
• Manage logbooks for the cleanroom and assist with document retention.
• Assist with inventory of the cleanroom.
• Other duties as assigned

Skills

Cleanroom experience

Effective communication

Attention to detail

Time management

Team collaboration

Education

High school diploma or equivalent

Job description

Fagron US is seeking a Cleanroom Specialist to support sterile manufacturing by reviewing batch records for cGMP compliance, updating SOPs, and assisting with process improvements and production scheduling.

The role also manages cleanroom logbooks, supports document retention, and helps maintain inventory accuracy. Candidates should have at least two years of cleanroom manufacturing experience and strong attention to detail.