GMP Cleanroom Specialist 3rd Shift Only (10:30 pm - 6:00 am)

Nivagen Pharmaceuticals•Sacramento, CA

8d•$23 - $28•Onsite

About The Position

The Cleanroom Cleaner performs routine and specialized cleaning of Grade A through Grade D cleanroom environments. The role helps ensure the cleanliness and sterility of classified manufacturing areas in support of aseptic processing and regulatory compliance. The position is based at Nivagen Pharmaceuticals Inc. in Sacramento, California, and is designated for a third shift. The posting lists shift hours inconsistently: 10:30 pm–6:00 am in the title and 10:00 pm–6:30 am under benefits.

Requirements

High school diploma or equivalent.
At least 2 years of prior experience in a cGMP-regulated or cleanroom environment.
Familiarity with safety regulations and quality control processes in pharmaceutical manufacturing.
Understanding of GMP, SOPs, and regulatory requirements related to cleanroom environments.
Strong attention to detail and organizational skills, and the ability to follow precise instructions.
Ability to perform physically demanding tasks, including standing for extended periods, lifting, and operating cleaning equipment.

Nice To Haves

A degree in Chemistry or Microbiology, or experience in sterile cleaning and/or aseptic technique.
Experience in cleanroom cleaning or a pharmaceutical manufacturing environment; priority will be given to applicants with this experience.

Responsibilities

Clean and sanitize Grade A, B, C, and D cleanrooms, including airlocks, corridors, and material transfer zones.
Follow approved Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs) to maintain aseptic conditions.
Prepare cleaning agents and disinfectant solutions, including alcohol-based disinfectants and sporicidal agents, according to specifications.
Complete and maintain cleaning logs, checklists, and records accurately, with attention to traceability and data integrity.
Perform daily, weekly, and monthly cleaning tasks according to the Master Cleaning Schedule (MCS).
Wear appropriate cleanroom gowning and Personal Protective Equipment (PPE) for the area classification and activity.
Handle and store cleaning materials and equipment appropriately to prevent contamination.
Immediately report facility or equipment anomalies, contamination risks, and deviations from procedures to supervisors.
Support internal and external audits by maintaining cleanliness and documentation readiness.
Collaborate with Quality Assurance, Facilities, and Manufacturing teams to uphold regulatory and safety standards.