QC Microbiology Associate II – GMP Lab & Data Integrity

B. Braun US Pharmaceutical Manufacturing LLC; Irvine (CA); On-site; USD 36,000 - 45,000; Full time

Job summary

B. Braun Medical Inc. is seeking a Microbiology II professional to support microbiological testing and monitoring within a GMP-regulated pharmaceutical manufacturing environment in Irvine, CA.

This onsite role collaborates with Quality, Manufacturing, and Laboratory teams to ensure compliance with cGMP, GLP, USP, and FDA requirements. Responsibilities include routine testing of raw materials and finished products, document data in LIMS, and participate in investigations and continuous

Qualifications

• Bachelor's degree in Microbiology or related field.
• 1-2 years of related lab experience if degree obtained.
• Experience in GMP/GLP regulated environment.

Responsibilities

• Perform routine microbiological testing of raw materials and finished products.
• Maintain laboratory records, logbooks, and LIMS entries in compliance with ALCOA, GDP, and data integrity requirements.
• Support investigations and non-routine testing and continuous improvement activities.
• Ensure compliance with cGMP, GLP, SOPs, USP standards, and FDA regulations.

Skills

Microbiology testing

Aseptic techniques

Data analysis

Documentation

Education

Bachelor's in Microbiology

Tools

LIMS

Microsoft Office

Job description

B. Braun Medical Inc. is seeking a Microbiology II professional to support microbiological testing and monitoring within a GMP-regulated pharmaceutical manufacturing environment in Irvine, CA.

This onsite role collaborates with Quality, Manufacturing, and Laboratory teams to ensure compliance with cGMP, GLP, USP, and FDA requirements. Responsibilities include routine testing of raw materials and finished products, document data in LIMS, and participate in investigations and continuous