GMP QC Microbiology Associate Scientist

ProBio; Pennington (NJ); On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with company match

Paid parental leave

Paid time off

Job summary

GenScript USA Inc/ProBio Inc. seeks a QC Microbiology professional to lead GMP-compliant lab activities supporting a wide range of clinical materials. You will implement validation programs, maintain QC tests, and ensure cGMP adherence across environmental monitoring, sterility, and related assays.

You will collaborate with the Microbiology Manager, contribute to process development, and support technology transfer within a CDMO framework to deliver patient-impacting products.

Qualifications

• Master’s degree with 1 year of relevant work experience or a Bachelor’s with 3 years’ experience; degree in Microbiology, Molecular Biology, Biochemistry, or related field.

Responsibilities

• Set up, develop and maintain a GMP QC-Microbiology Lab.
• Participate in EMPQ, cleanroom validation, and related activities/documents.
• Follow cGMP in QC testing.
• Perform QC microbiology tasks: Environmental Monitoring, Plate Reads, Water and Gas Testing, Gram Staining, Growth Promotion, Bioburden, Gowning qualifications.
• Test compounded sterile and non-sterile pharmaceuticals.
• Support lab personnel and ensure SOPs and safety standards.

Skills

GMP documentation

Environmental monitoring

Mycoplasma testing

Cell culture assays

Problem solving

Team collaboration

Education

Master's degree with 1 year experience

Bachelor's degree in Microbiology/Molecular Biology/Biochemistry

Job description

GenScript USA Inc/ProBio Inc. seeks a QC Microbiology professional to lead GMP-compliant lab activities supporting a wide range of clinical materials. You will implement validation programs, maintain QC tests, and ensure cGMP adherence across environmental monitoring, sterility, and related assays.

You will collaborate with the Microbiology Manager, contribute to process development, and support technology transfer within a CDMO framework to deliver patient-impacting products.