We're looking for a Scientist II, working in the Pharmaceuticals & Medical Products industry in Ridgefield, Connecticut, United States.
Assume GLP and non-GLP bioanalytical responsibility for both small molecule and protein drug candidates under supervision. This encompasses LCMS-based bioanalytical method development and validation, sample analysis, reporting bioanalytical data and responding to auditing by QC and QA.
Perform all work in conformance with applicable regulations (GLP and SOPs) and perform all work in a safe manner.
Perform data analysis and report writing with a high level of integrity and ethics.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Pharmaceutical, biotechnology or CRO experience is highly desirable
Experience in developing and validating LCMS bioanalytical methods
Experience in LCMS protein assay and immunoassay is preferred
Experience working in a GLP/GCP environment
Ability to operate and maintain laboratory equipment with some supervision
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.