LCMS Method Development Scientist III

LabcorpIndianapolis, IN
5d$70,000 - $100,000

About The Position

Method Development Scientist Work Schedule: Monday - Friday Day shift Method Develop Scientist III Job Responsibilities: Undertakes original research that includes developing and confirming highly sensitive, reliable assay methodologies for the rapid and accurate analysis of pharmaceuticals in biological fluids and tissues. Performs complex analytical methods on biological matrices, often involving problem solving situations. Applies and interprets scientific theories, concepts, techniques, and regulatory requirements in bioanalytical and mass spectrometry studies and accepts leadership role in developing scientific approaches. Acts as research scientist, in a team work setting, for technical direction on complex bioanalytical and mass spectrometry projects. Responds to unscheduled deadlines, client needs, crises, etc. without neglecting other duties. Produces reports for reliable, sensitive, and validated methods of analyses. Authors scientific papers which are published in peer reviewed journals. Participates in client visits. Contributes to long-range planning and technical policies of the department. Performs other related duties as assigned. Minimum Qualifications: Bachelor's Degree analytical chemistry, or equivalent degree Three or more years of related experience. (Relevant experience may be substituted for education.) Preferred Qualifications: PhD in analytical chemistry, or equivalent degree, with 2 years of related experience. Working experience with oligo, ADC etc. method development is highly desired. Additional Job Standards: Experience and knowledge of analytical instrumentation (e.g. - HPLC, LC/MS/MS) Proven track record of analytical method development Skilled in conducting research, compiling data, data interpretation, and writing reports according to regulatory requirements Skilled in performing scientific presentations and preparing scientific publications Knowledge of laboratory automation software, system software, and Microsoft applications Effective oral and written communication skills Overtime and weekend work as required by client Mandatory immunization and screenings as required by the client/vendor May be required to attend technical conferences as required

Requirements

  • Bachelor's Degree analytical chemistry, or equivalent degree
  • Three or more years of related experience. (Relevant experience may be substituted for education.)
  • Experience and knowledge of analytical instrumentation (e.g. - HPLC, LC/MS/MS)
  • Proven track record of analytical method development
  • Skilled in conducting research, compiling data, data interpretation, and writing reports according to regulatory requirements
  • Skilled in performing scientific presentations and preparing scientific publications
  • Knowledge of laboratory automation software, system software, and Microsoft applications
  • Effective oral and written communication skills

Nice To Haves

  • PhD in analytical chemistry, or equivalent degree, with 2 years of related experience.
  • Working experience with oligo, ADC etc. method development is highly desired.

Responsibilities

  • Undertakes original research that includes developing and confirming highly sensitive, reliable assay methodologies for the rapid and accurate analysis of pharmaceuticals in biological fluids and tissues.
  • Performs complex analytical methods on biological matrices, often involving problem solving situations.
  • Applies and interprets scientific theories, concepts, techniques, and regulatory requirements in bioanalytical and mass spectrometry studies and accepts leadership role in developing scientific approaches.
  • Acts as research scientist, in a team work setting, for technical direction on complex bioanalytical and mass spectrometry projects.
  • Responds to unscheduled deadlines, client needs, crises, etc. without neglecting other duties.
  • Produces reports for reliable, sensitive, and validated methods of analyses.
  • Authors scientific papers which are published in peer reviewed journals.
  • Participates in client visits.
  • Contributes to long-range planning and technical policies of the department.
  • Performs other related duties as assigned.

Benefits

  • Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
  • Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.
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