Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

R&D Chemist II

Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
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.

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
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.

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 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

Preferred Qualifications

Analytical Skills (e.g., statistical, risk analysis, engineering analysis)
Team player
Interpersonal Skills
Drives for results.
High level of attention to detail
Adaptability

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

The base pay for this position is
$54,000.00 - $108,000.00
In specific locations, the pay range may vary from the range posted.

JOB FAMILY:
Operations Quality

DIVISION:
TOX ARDx Toxicology

LOCATION:
United States > Gretna : 1111 Newton Street

ADDITIONAL LOCATIONS:

WORK SHIFT:
3Rd Shift (United States Of America)

TRAVEL:
Yes, 10 % of the Time

MEDICAL SURVEILLANCE:
No

SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Routine work with chemicals, Work requiring repeated bending, stooping, squatting or kneeling

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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R&D Chemist II