Pharma LCMS/GCMS-MS Analyst — Method Dev & Validation

LabCommunity.org; Norway; On-site; NOK 600,000 - 800,000; Full time

Job summary

LabCommunity.org in Norway seeks experienced analytical professionals to operate LCMS-MS and GCMS-MS systems for batch analysis, method development and method validation of finished drug products.

Candidates with 2–10 years of hands-on LCMS/GCMS expertise and familiarity with genotoxic impurities, nitrosamines, and Extractable & Leachables are preferred; those from non-pharma backgrounds with GMP exposure are welcome to shift into pharma.

Qualifications

• 2–10 years of hands-on LCMS/GCMS experience required in batch analysis, method development and validation.
• Experience identifying Genotoxic Impurities, Nitrosamines and Extractable & Leachables is essential.
• Special preference for those with large molecule testing exposure.

Responsibilities

• Operate LCMS-MS / GCMS-MS instruments for batch analysis and release testing.
• Perform method development and validation for Genotoxic Impurities, Nitrosamines, and Extractable & Leachables.
• Coordinate with QA/QC to ensure GMP-compliant data and documentation.

Skills

LCMS/GCMS

Method development

Method validation

Genotoxic impurities

Nitrosamines

Extractable & Leachables

GMP exposure

Tools

LCMS-MS

GCMS-MS

Job description

LabCommunity.org in Norway seeks experienced analytical professionals to operate LCMS-MS and GCMS-MS systems for batch analysis, method development and method validation of finished drug products.

Candidates with 2–10 years of hands-on LCMS/GCMS expertise and familiarity with genotoxic impurities, nitrosamines, and Extractable & Leachables are preferred; those from non-pharma backgrounds with GMP exposure are welcome to shift into pharma.