Senior Microbiology LIMS Analyst — GMP & LabVantage

Sgs; Fairfield (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Tuition reimbursement

Growth opportunities

Job summary

SGS, the world’s leading testing, inspection and certification company, seeks a Senior Analyst for Pharmaceutical Microbiology LIMS in New Jersey. You will translate lab processes into validated LabVantage LIMS solutions and collaborate with QC Microbiology, QA, Validation and IT teams.

Your responsibilities include configuring LIMS, developing test templates and workflows, and validating systems to ensure GMP, 21 CFR Part 11 and data integrity compliance across sites.

Qualifications

• Bachelor’s or Master’s in Microbiology, Biology, Pharmaceutical Sciences, or Biotechnology.
• 5+ years of GMP pharmaceutical laboratory experience.
• Experience with USP/EP/JP/BP methods and related testing.

Responsibilities

• Configure and maintain LabVantage LIMS for pharmaceutical microbiology testing.
• Develop and support test templates, specifications, sampling plans, calculations, and approval workflows.
• Translate regulatory requirements into system configurations and specs.
• Support system validation activities including IQ/OQ/PQ documentation.
• Ensure GMP, 21 CFR Part 11, and data integrity compliance.
• Collaborate with QC Microbiology, QA, Validation, and IT to implement methods and enhancements.

Skills

LIMS knowledge

GMP microbiology

Regulatory knowledge

Project coordination

LabVantage proficiency

Education

Bachelor’s or Master’s in Microbiology/Biology/Pharmaceutical Sciences/Biotechnology

Tools

LabVantage LIMS

Job description

SGS, the world’s leading testing, inspection and certification company, seeks a Senior Analyst for Pharmaceutical Microbiology LIMS in New Jersey. You will translate lab processes into validated LabVantage LIMS solutions and collaborate with QC Microbiology, QA, Validation and IT teams.

Your responsibilities include configuring LIMS, developing test templates and workflows, and validating systems to ensure GMP, 21 CFR Part 11 and data integrity compliance across sites.