QC Analyst- Quality Control Analytical Instrument & Method Development
On-site in Thousand Oaks, CA
$54-$68/hr (pay rate varies based on experience)
Fully Vaccinated: Yes
Summary:
A dynamic, pharmaceutical/biotech GxP compliance & consulting firm is looking to bring on a QC Analyst centered around Analytical Instrument and Method Development.
This is a fully on-site role in Thousand Oaks, CA that will start as a contract position with opportunity for conversion to a permanent role.
Key Responsibilities:
- Plan, Provide, Execute & Implement analytical assays
- Draft and/or revise SOP's and Protocols
- Various Assay work including;
- Protein/Bio-Assays ELISA and other related assays
- Host Cell Protein (HCP) assays
- Enzymatic activity assay
- Host DNA Assay (qPCR) method
- Substance clearance assay
- Experience with Mammalian/Human cell cultures including;
- Cell count and culture maintenance
- Automated Cell Counting (LUNA Cell Counter)
- Metabolite Analysis (BioProfile FLEX Instrument)
- Cellular Morphology and Viability
- Strong demonstrated method troubleshooting capability
Key Qualifications:
- 5-7 years' experience in either manufacturing, quality, or engineering within the pharmaceutical/biotech space
- Bachelor's Degree or superior in science related field (BA/BS)
- Knowledge of GMP compliance requirements for Quality Control Labs
- Hands on instrumental experience is a must
- Experience providing professional services utilizing at least one of the following;
- SDS-PAGE (reduced and non-reduced method)
- Silver Stained and Coomassie
- HPLC Methodology/Assays for large molecule (proteins) including:
- SEC (Size Exclusion Analysis) assay
- %FG (Relative Formyl glycine Content)
- Peptide Mapping
- Glycan Analysis / Sialic Acid Content
- High Performance Anion Exchange Analysis
Next Steps:
If interested please apply and contact Emily with any questions,