QC Microbiology Tech I: GMP Testing & Env Monitoring

Planet Pharma; Frederick (MD); Sur place; USD 25 000 - 36 000; Plein temps

Résumé du poste

Planet Pharma in Frederick, MD is seeking a motivated QC Microbiology Technician to join our new commercial cell therapy production center. You will support microbiological testing, environmental monitoring, and QA collaboration in a GMP environment.

Responsibilities include sampling classified manufacturing areas, receiving and storing media, monitoring waste, and maintaining compliance with GMP, safety and SOPs.

Qualifications

• 1+ year microbiology lab/Environmental Monitoring experience or equivalent
• GMP and SOP familiarity for commercial manufacturing environments
• Strong documentation and data integrity practices

Responsabilités

• Perform microbiological testing and environmental monitoring in GMP environments
• Maintain cleanroom and laboratory areas in accordance with procedures
• Receive, inspect, store, and document microbiological media and supplies
• Monitor biohazardous waste and coordinate disposal with EHS as needed
• Support validation, qualification, development, and manufacturing activities
• Document activities accurately and contemporaneously
• Collaborate with Quality Control, Manufacturing, and Quality Assurance teams
• Perform additional duties and special projects as assigned by management
• Ensure responsibilities can be delegated to trained deputies when needed

Connaissances

Microbiology lab experience

Environmental Monitoring

GMP knowledge

Laboratory safety

Analytical skills

Formation

Associate's degree in Microbiology or related field

High school diploma with relevant experience

Outils

MS Word

Excel

PowerPoint

Description du poste

Planet Pharma in Frederick, MD is seeking a motivated QC Microbiology Technician to join our new commercial cell therapy production center. You will support microbiological testing, environmental monitoring, and QA collaboration in a GMP environment.

Responsibilities include sampling classified manufacturing areas, receiving and storing media, monitoring waste, and maintaining compliance with GMP, safety and SOPs.