6 quality control method development specialist jobs at 6 companies in United States
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Quality Control Method Development Specialist
Henderson, Nevada, United States
OnsiteFull Time
3+ YOEBachelor’s degree in chemistry, biochemistry, pharmaceutical sciences, or a natural or physical science; 3+ years in analytical method development, validation, or laboratory quality control; regulated laboratory experience and instrumentation expertise.
Microsoft Office, HPLC, GC, ICP-MS, UV/VIS, HPTLC, Protein Analyzer, USP, AOAC, ICH, ISO/IEC 17025, cGMP, CAPA, PPE
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Quality Control Specialist II
Morrisville, North Carolina, United States
$90k-$166k/yr OnsiteFull Time
Bachelor's, master's, or PhD in chemistry, pharmaceutical sciences, or related science; cGMP experience; analytical method development, validation, transfer, troubleshooting, and hands-on HPLC, GC, UPLC, or LC-MS experience.
HPLC, UPLC, GC, LC-MS, ICP, Empower CDS, LabWare LIMS, dissolution, spectroscopy, ALCOA+, ICH Q2, ICH Q10, ICH Q14, Quality Management Systems (QMS), Standard Operating Procedure (SOP), Statistical Process Control (SPC)
1mo
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Senior Quality Control Specialist Series
Woodside, New York, United States
$90k-$116k/yr OnsiteFull Time
6+ YOEBachelor's in engineering/tech or 60+ college credits plus significant quality control experience; 6+ years experience in quality control, statistical methods, test procedure development, and documentation management.
Microsoft Office, CAD, document conversion tools
1mo
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Quality Control Specialist
Portsmouth, New Hampshire, United States
OnsiteFull Time
3+ YOE3+ years QC experience in GMP/pharma/biotech labs, associate's or bachelor's in life science preferred, experience with analytical or microbiological methods, knowledge of cGMP and data integrity, familiarity with LIMS/TrackWise/DMS.
LIMS, TrackWise, DMS
2mo
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Specialist, Quality Control Analytical
El Segundo, California, United States
$43-$47/hr OnsiteFull Time
4+ YOEBachelor's +6 yrs or Master's +4 yrs in analytical chemistry or related; experience in method development/validation/transfer, lot release, stability, GMP knowledge, technical writing, and QC data review.
2mo
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Principal Specialist – Quality Control Microbiology Lead (Baltimore, MD, US, 21224)
Baltimore, Maryland, United States
OnsiteFull Time
Bachelor's in chemistry/biochemistry/chemical engineering or related required (Master's preferred); subject-matter expertise in QC for biologics; experience in microbiological testing, environmental monitoring, method validation, regulatory inspections, and team leadership.