R&D Chemist II

Abbott Laboratories • Gretna, LA

92d • $54,000 - $108,000

About The Position

The position of R D Chemist II 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.

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 PowerPoint.
• Experience with electronic document control systems such as Agile.
• Experience with Hamilton Automated Liquid Handler instruments.
• Experience with Multiqunt and Analyst Quantitation software.
• Experience with LC-MS/MS & GC/MS.

Nice To Haves

• 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.
• Training of personnel on 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

• Career development with an international company.
• Free medical coverage in the Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• Excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement.
• Freedom 2 Save student debt program.
• FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Computer and Electronic Product Manufacturing
• Education Level: Bachelor's degree