GMP Cleanroom Technician - 3rd Shift & Benefits

Nivagen Pharmaceuticals Inc; Sacramento (CA); On-site; USD 32,000 - 39,000; Full time

Benefits offered by this job

Pay range $23-$28 per hour (3rd shift)

Yearly Bonus Eligible

Medical, Dental and Vision

Paid Time Off

Job summary

Nivagen Pharmaceuticals Inc. is seeking a dedicated Cleanroom Cleaner to perform routine and specialized cleaning of Grade A through Grade D cleanroom environments. This role ensures cleanliness and sterility to support aseptic processing and regulatory compliance.

Responsibilities include following SOPs, preparing cleaning agents, maintaining logs, and supporting audits while collaborating with QA, Facilities, and Manufacturing teams to uphold safety standards.

Qualifications

• Minimum 2 years in a cGMP-regulated or clean room environment.
• Experience with safety regulations and quality control processes in pharmaceutical manufacturing.
• Priority for candidates with cleanroom cleaning or pharmaceutical manufacturing experience.
• High school diploma required; degree in Chemistry or Microbiology preferred.

Responsibilities

• Clean and sanitize Grade A–D cleanrooms and surrounding areas.
• Follow SOPs and cGMPs to maintain aseptic conditions.
• Prepare cleaning agents and disinfectants per specifications.
• Maintain cleaning logs, checklists and records with accuracy and traceability.
• Support internal and external audits with documentation readiness.

Skills

GMP knowledge

SOP adherence

Regulatory requirements

Attention to detail

Organizational skills

Following precise instructions

Education

High school diploma or equivalent

Degree in Chemistry or Microbiology (preferred)

Job description

Nivagen Pharmaceuticals Inc. is seeking a dedicated Cleanroom Cleaner to perform routine and specialized cleaning of Grade A through Grade D cleanroom environments. This role ensures cleanliness and sterility to support aseptic processing and regulatory compliance.

Responsibilities include following SOPs, preparing cleaning agents, maintaining logs, and supporting audits while collaborating with QA, Facilities, and Manufacturing teams to uphold safety standards.