R&D Chemist II: Method Validation & LC-MS/MS Expert

R&D Chemist II This position is within our Toxicology Laboratories located in Gretna, LA. Primary duties include documentation of validation projects for laboratory testing methodology for the determination of drugs and metabolites in biological matrices. This role will be instrumental in providing accurate and timely test results to our clients. The Opportunity Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for the workplace, healthcare providers, and individuals. What You’ll Work On Assist R&D Manager with designing studies for method development Perform method validation activities following laboratory policies and applicable regulatory guidelines (NLCP, CAP, etc) Research and present literature and its applications to applicable method development opportunities Collaborate with R&D Chemists at other Abbott laboratory sites Perform statistical evaluation and cost analysis to justify method development and improvement projects Draft and collaborate on validation plans and validation approval documents Perform IQ, OQ, and PQ on new instruments Programming new methods on instruments Training of personnel on new sample prep methods, basic method development and troubleshooting Preparation of solutions for validation experiments Extraction of drugs from biological matrices Submission of samples on LC-MS/MS, GC/MS and AU Screening instrumentation Review of validation data using software such as Sciex Analyst and MultiQuant Data entry of validation results Performing basic statistical analysis with Microsoft Excel Properly documenting sample prep procedures Analyzing data from validation batches Determining success of validation experiments Review of Standard Operating Procedures and Validation Reports to ensure consistency Support production team with solutions and sample preparation Present project results and recommendations to department management Proactively and cooperatively communicate with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise Maintain and meet the highest standards in quality and regulatory compliance Follow, understand and comply with SOP’s and safety policies Perform any other duties as designated by the Manager, Technical and Instrumentation, or dictated by the needs of the laboratory Required Qualifications Bachelor’s degree from an accredited college or university in chemistry, biochemistry or related field 2 years of experience Experience with Microsoft Word, Excel and Power Point Experience with electronic document control systems such as Agile Experience with Hamilton Automated Liquid Handler instruments Experience with MultiQuant and Analyst Quantitation software Experience with LC‑MS/MS & GC/MS Preferred Qualifications Master's degree in chemistry, biochemistry or related field 2 years of experience within R&D Competencies Analytical Skills (e.g. statistical, risk analysis, engineering analysis) Team player Interpersonal Skills Drives for results High level of attention to detail Adaptability Salary The base pay for this position is $55,300.00 – $110,700.00. In specific locations, the pay range may vary from the range posted. Equal Opportunity Statement Abbott is an Equal Opportunity Employer, committed to employee diversity. #J-18808-Ljbffr Abbott Laboratories