HTP Analytical QC Associate Scientist
GenScript · Piscataway, NJ · 4 wk ago
On-siteAnalyst$60k–$75k/yrFull-time
Key Responsibilities
- Perform routine and non-routine analytical and QC testing to evaluate protein identity, purity, and quality attributes.
- Execute a range of protein characterization assays, including:
- HPLC / UPLC (e.g., SEC, RP, IEX)
- Capillary Electrophoresis (CE, iCE/cIEF)
- SDS-PAGE
- Western blot
- LC-MSE
- Endotoxin assays
- Prepare samples, reagents, buffers, and standards in accordance with established protocols and assay requirements.
- Analyze, interpret, and document experimental data in ELN, LIMS, or equivalent systems, ensuring compliance with data integrity standards (e.g., ALCOA+ principles).
- Support method troubleshooting and optimization, ensuring assay robustness, reproducibility, and consistency across runs.
- Maintain laboratory instruments and ensure proper calibration and performance, supporting compliance with quality and safety standards.
- Collaborate with cross-functional teams (e.g., protein production, process development) to support project timelines and deliverables.
- Contribute to continuous improvement initiatives, including method refinement, workflow efficiency, and data quality enhancement.
Qualifications
- BS or MS in Biochemistry, Analytical Chemistry, Biotechnology, or a related field with 2+ years of relevant experience in protein analytical characterization or QC.
- Hands-on experience with protein analytical techniques such as HPLC/UPLC, CE, SDS-PAGE, Western blot, LC-MS, or endotoxin assays.
- Familiarity with protein characterization workflows, including purity, aggregation, and identity analysis.
- Experience with laboratory data systems (ELN, LIMS, or similar) and strong documentation practices.
- Strong attention to detail and commitment to data integrity, accuracy, and reproducibility.
- Experience in a CRO/CDMO or regulated QC environment is preferred.