GMP Cleanroom Pro — 3rd Shift Aseptic Specialist

Nivagen Pharmaceuticals; Sacramento (CA); Sur place; USD 32 000 - 39 000; Plein temps

Avantages offerts par ce poste

Yearly Bonus Eligible

Medical, Dental and Vision

Paid Time Off

Résumé du poste

Nivagen Pharmaceuticals in Sacramento is seeking a GMP Cleanroom Specialist for the 10:30 pm–6:00 am shift. The role cleans Grade A–D cleanrooms and surrounding areas to support aseptic processing and regulatory compliance.

You will follow SOPs and cGMPs, prepare cleaning agents, maintain logs, wear appropriate PPE, and collaborate with QA, Facilities, and Manufacturing to ensure quality and safety.

Qualifications

• High school diploma or equivalent. Degree in Chemistry, Microbiology, and/or experience in Sterile Cleaning and/or Aseptic Technique preferred.
• Minimum 2 years of experience in a cGMP-regulated or clean room environment.
• Familiarity with safety regulations and quality control in pharmaceutical manufacturing.
• Priority for candidates with cleanroom or pharmaceutical manufacturing experience.

Responsabilités

• Clean and sanitize cleanrooms from Grade A to D and surrounding areas.
• Follow SOPs and cGMPs to maintain aseptic conditions.
• Prepare cleaning agents and disinfectants per specifications.
• Complete and maintain cleaning logs and records with accuracy.
• Perform tasks per Master Cleaning Schedule (MCS).
• Wear proper cleanroom gowning and PPE as required.
• Store cleaning materials to prevent contamination.
• Report anomalies or deviations to supervisors promptly.
• Support audits with documentation readiness.
• Collaborate with QA, Facilities, and Manufacturing to uphold standards.

Connaissances

Attention to detail

Organizational skills

Follow precise instructions

GMP knowledge

cGMP familiarity

Safety regulations

Formation

High school diploma

Chemistry/Microbiology background

Description du poste

Nivagen Pharmaceuticals in Sacramento is seeking a GMP Cleanroom Specialist for the 10:30 pm–6:00 am shift. The role cleans Grade A–D cleanrooms and surrounding areas to support aseptic processing and regulatory compliance.

You will follow SOPs and cGMPs, prepare cleaning agents, maintain logs, wear appropriate PPE, and collaborate with QA, Facilities, and Manufacturing to ensure quality and safety.