You will be a valued contributor to the Analytical Development team and across the company utilizing your experience in protein characterization, purification, and method development (HPLC, LC-MS, LC-MS/MS, CE) to advance all molecules in our pipeline.

Develop and execute test methods in support of cell and gene therapy Process Development activities (e.g., SEC-HPLC, RP-HPLC, CESDS/cIEF, LCMS intact mass/peptide mapping, etc.) Hands-on experience with the following assays: High Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), Liquid Chromatography coupled with Mass Spectrometry (LC-MS), capillary electrophoresis (CE.

HPLC, RP-HPLC, SEC, Agarose Gel Electrophoresis, UPLC, CE, IEF, Protein Purity Assay, Peptide Mapping, DNA Sequencing and/or UV/Vis Spectrometry preferred. HPLC, Chromatography (Ion Exchange, SEC, RP-HPLC, Residual Analytes.

Working knowledge of analytical chemistry, HPLC-UV/RI/PDA, GC-FID, ICP-OES, protein and fat analyzer, FT-NIR (preferred) Working knowledge of analytical chemistry, HPLC-UV/RI/PDA, GC-FID, ICP-OES, protein and fat analyzer, FT-NIR (Preferred.

Perform purification of peptides/peptide conjugates using various prep-HPLC techniques. Perform characterization of peptides/ peptide conjugates using LC-MS, HPLC, UPLC, and other techniques.

Demonstrated practical ability to develop methods for isolation, characterization, and quantification of both drug substances and drug products of small molecules or/and large molecules using conventional chromatography techniques and analytical instruments including GC, GC/MS, HPLC, ELISA, MSD or/and LC/MS.

Hplc, Chemistry, Analytical chemistry, Laboratory, Gmp, Wet chemistry, Gas chromatography, Gcms, method validation, Pharmaceutical. Knowledge of various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectrum, HPLC, GC, atomic absorption.

The successful candidate must demonstrate a depth and breadth of knowledge in chromatography, data analysis, and problem solving in applications, HPLC hardware, and CDS software. Perform online and offline HPLC analyses on a variety of sample types and execute established robot protocols for sample preparation.

You will perform complex compounding, manufacturing (cyclotron and chemistry module operation) and quality control processes (utilizing analytical equipment TLC, HPLC, GC), under supervision as required by State and Federal law.

Proficient in performing multiple protein assays such as ELISA, SDS-PAGE, Western blotting, HPLC, CE, cell-based assays, immunoassays and/or molecular assays such as q-PCR.Ability to work on multiple projects.

Author and revise SOPs, deviations, CRs and LIRs. Areas of responsibility include but are not limited to testing samples for molecular biology techniques such as water content, ELISA, western blot, SDS-PAGE and/or analytical chemistry techniques such as SEC-HPLC, CEX-HPLC, IEX HPLC as needed.

Exp. with with GLP/GMP requirements, cUSP as well as other Compendia required - Exp. with some combination of the following: HPLC/GC/ICP Analysis, wet chemistry and bench chemistry, pH, UV/Vis, FTIR, Automatic titration.

Analytical Chemistry Equipment and Processes (HPLC, GC, TLC) Siemens Healthineers' PETNET Solutions, a global PET radiopharmaceutical network, leads the way in industry expertise. Analytical Chemistry Equipment and Processes (HPLC, GC, TLC.

A strong background in polymer HPLC analysis with at least 0-5 years industrial/academic experience related to polymers. Develop quantitative analysis using HPLC with UV, CAD, and ELSD detectors.

Must know how to operate GC-MS, LC-MS, HPLC, TLC, ICP-MS, etc. Able to follow ready established test procedures(Client, or EP, or USP) to run testing using GC , HPLC , TLC. Must know how to operate GC-MS, LC-MS, HPLC, TLC, ICP-MS, etc.