Quality Control Scientist: GMP & Data Analytics

INVIVOSCRIBE INC; San Diego (CA); On-site; USD 85,000 - 95,000; Full time

Job summary

Invivoscribe is hiring a Quality Control Scientist I in San Diego to support QC testing, validation, and data analysis within a GMP-regulated setting. This role emphasizes method development, SOP maintenance, and documentation quality across the QC workflow.

The ideal candidate has an MS in a scientific field and 4+ years of biotech QC experience, with hands-on use of molecular biology techniques and multiple QC instruments. Join a global leader in precision diagnostics.

Qualifications

• M.S. degree in a scientific discipline with 4+ years in biotech QC; advanced degree preferred.
• Experience developing, validating, optimizing, troubleshooting, or implementing QC methods.
• Strong background in molecular biology and GMP-regulated QC environments.
• Proficient with statistical QC and data analysis.
• Familiarity with SOPs, MBRs, QCACs, QTPs, PSs and Oracle systems.

Responsibilities

• Develops, improves and validates QC testing methods and processes.
• Generates QC validation protocols and reports.
• Supports transfer and implementation of new or modified test methods into routine QC operations.
• Creates and maintains SOPs, acceptance criteria, and QC documents.
• Performs QC data analysis to identify trends and improvement opportunities.
• Maintains QC metrics, reports, and visualizations for technical reviews.
• Leads investigations with RCA, CAPAs, and related quality events.

Skills

Molecular biology

Statistical quality control

Laboratory automation

GMP QC experience

Data analysis

Education

MS degree in a scientific discipline

4+ years biotech QC experience

Tools

3500xl Dx

ABI 7500 Dx

MiSeq Dx

BioTek plate fluorometer

QiaCube

2100 Bioanalyzer

TapeStation

LabChip Gx

NanoDrop

iBright

Job description

Invivoscribe is hiring a Quality Control Scientist I in San Diego to support QC testing, validation, and data analysis within a GMP-regulated setting. This role emphasizes method development, SOP maintenance, and documentation quality across the QC workflow.

The ideal candidate has an MS in a scientific field and 4+ years of biotech QC experience, with hands-on use of molecular biology techniques and multiple QC instruments. Join a global leader in precision diagnostics.