NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION.
Job Duties
- Independently develop and validate bio-analytical methods for quantitative determination of test items in biological matrices and formulations using liquid chromatography-mass spectrometry (LC-MS)/MS and high performance liquid chromatography (HPLC) with various sample preparation techniques according to the FDA good laboratory practices (GLP) regulations and guidance
- Complete stability testing in support of study sample analysis
- Analyze clinical and non-clinical samples according to the standard operating practices (SOP) and regulatory requirements using chromatographic assays including LC-MS/MS and HPLC
- Maintain laboratory, equipment, materials, chemicals, consumables, samples, solvents, and solutions to ensure cleanliness, adequate inventory and organization, clear labeling, current calibrations, personal safety, and that nothing for use has expired or compromised
- Complete laboratory notebooks and other study records as per the Good Documentation Practices
- Prepare and respond to change control, CAPA, and deviation reports, and respond to audit observations
- Author and peer review computerized system validation, bio-analytical methods, SOPs, and study plans and reports
- Train and mentor team members on laboratory procedures, instrumentation, software, and equipment
If interested, please e-mail your resume to careers@nebiolab.com.