QC Micro Analyst – Microbiology GMP Lab (Sun-Wed Shift)

Spectraforce Technologies

Summit (NJ)

On-site

USD 60,000 - 90,000

Full time

14 days+

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Job summary

Spectraforce Technologies is seeking a QC Micro Analyst for a 6-month assignment in Summit, NJ. The role involves microbiological testing, environmental monitoring, and related QC tasks in a regulated environment.

You will perform endotoxin and PCR-based tests, maintain documents, and support continuous improvement initiatives while ensuring adherence to USP, EP, and FDA requirements.

Qualifications

  • This role requires a Bachelor's in Microbiology or related field with 3+ years in a regulated manufacturing environment.
  • Master’s degree is strongly preferred.
  • Familiarity with USP, EP, JP and FDA microbiology testing requirements.
  • Proficient in MS Word and Excel; capable of handling data and reports.

Responsibilities

  • Carry out routine and non-routine microbiological testing per SOPs.
  • Ensure compliance with cGMP, USP, EU and other regulations at all times.
  • Communicate effectively with QC peers and management.
  • Assist in troubleshooting and problem solving in day-to-day operations.
  • Perform environmental monitoring and aseptic process qualifications as needed.
  • Conduct PCR-based microbial identification and endotoxin testing.
  • Maintain lab inventory and document results with Good Documentation Practices.
  • Support continuous improvement projects in QC and documentation.

Skills

Communication skills
Teamwork
Adaptability

Education

Bachelor's degree in Microbiology or related field
Master’s degree preferred

Tools

Microsoft Word
Microsoft Excel

Job description

Spectraforce Technologies is seeking a QC Micro Analyst for a 6-month assignment in Summit, NJ. The role involves microbiological testing, environmental monitoring, and related QC tasks in a regulated environment.

You will perform endotoxin and PCR-based tests, maintain documents, and support continuous improvement initiatives while ensuring adherence to USP, EP, and FDA requirements.

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