R&D Chemist II

Abbott Laboratories • Gretna, LA

7d • $55,300 - $110,700 • Onsite

About The Position

The position of R&D Chemist II is within Abbott Rapid Diagnostics' Toxicology Laboratories located in Gretna, LA. This role is instrumental in providing accurate and timely test results to clients by documenting validation projects for laboratory testing methodology for the determination of drugs and metabolites in biological matrices.

Requirements

• 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

Nice To Haves

• Master's degree in chemistry, biochemistry or related field
• 2 years of experience within R&D
• Analytical Skills (e.g. statistical, risk analysis, engineering analysis)
• Team player
• Interpersonal Skills
• Drives for results
• High level of attention to detail
• Adaptability

Responsibilities

• 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

Benefits

• Free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement
• The Freedom 2 Save student debt program
• FreeU education benefit

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level