Description
Summary:- Oversight of instrument installation and organization of laboratory space.
- The scientist should require minimal training and will support methods run on the instruments and participate in the maintenance of the instruments.
- Develop and validate ligand binding assays for regulated study support.
- In addition, the scientist will also conduct sample testing in support of regulated studies, maintain a GLP/GCLP compliant laboratory, and perform routine equipment maintenance and calibration.
Requirements:
- Experience with large molecule/biotherapeutics preferred. LC-MS experience not necessarily needed.
- 1 year of direct Pharma experience also desired.
- Bachelor's degree required.
- Candidates should have 2 to 4 years experience with ligand binding assays (ELISA, electrochemiluminescence, fluorescence - Gyros platform) for routine sample analysis.
- Prior experience with regulated (GLP and/or GCLP) studies is desirable.
- The candidate will need routine sample analysis using immunoassay techniques.
- Looking for someone with large molecule/biotherapeutic experience with proficiency in developing/validating ligand binding assays in a biohazardous Matrix (serum, plasma) and/or running LBAs for routine sample analysis in support of pharmacokinetic/toxicokinetic studies.
- The ligand binding assays would be to quantify a drug candidate, a biomarker for the drug candidate, and/or detecting an immune response to a drug candidate.
- Someone with ~3 years of pharma experience and/or has worked under GLP regulations is ideal.
- While they may have some proficiency in ligand binding assays (ELISA), that aspect of work did not appear to be used routinely.