2nd Shift QC Microbiologist — Regulated Lab, Impact

Atrium; Northvale (NJ); On-site; USD 59,000 - 72,000; Full time

Benefits offered by this job

Atrium Care Package

Job summary

Atrium is seeking a 2nd Shift QC Microbiologist in Northvale, NJ, to perform routine microbiological testing of water systems, raw materials, and finished products within a regulated environment.

You will interpret results, generate detailed reports, maintain data integrity, and mentor junior staff on testing methods and SOP compliance.

This Monday–Friday, 2nd shift role supports cGMP and FDA requirements, with collaboration across the quality team and external labs.

Qualifications

• 2–4 years of microbiology experience in a regulated lab.
• Hands-on microbiology techniques including aseptic technique, streak plating, culture maintenance, gram staining.
• Understanding of cGMP and FDA regulations.
• Strong data interpretation and reporting skills.

Responsibilities

• Perform routine microbiological testing of water systems, bulk chemicals, drug substances, and finished products.
• Conduct aseptic sampling of materials, air, and surfaces to monitor contamination.
• Analyze results, monitor trends, and prepare detailed reports ensuring data integrity.
• Prepare media and perform growth-promotion testing.
• Assist with calibration and maintenance of instruments.
• Coordinate testing with external contract labs.
• Draft investigation reports and non-conformance assessments.
• Maintain SOPs per regulatory requirements.
• Mentor junior staff on testing practices and SOP adherence.

Skills

2-4 years experience

aseptic technique

gram staining

data interpretation

communication

time management

ability to lift 50 lbs

Education

Bachelor's degree in Microbiology or Life Sciences

Tools

LIMS

Job description

Atrium is seeking a 2nd Shift QC Microbiologist in Northvale, NJ, to perform routine microbiological testing of water systems, raw materials, and finished products within a regulated environment.

You will interpret results, generate detailed reports, maintain data integrity, and mentor junior staff on testing methods and SOP compliance.

This Monday–Friday, 2nd shift role supports cGMP and FDA requirements, with collaboration across the quality team and external labs.