Analytical Scientist, Bioanalysis & Method Development

1100 Mylan Pharmaceuticals Inc.; Morgantown, Northern (WV, KY); Hybrid; USD 95,000 - 130,000; Full time

Job summary

Viatris is seeking a Scientist to set up and operate analytical equipment, develop and validate methods, and ensure accurate documentation for bioequivalence and PK studies. The role emphasizes quality data generation, compliance with GLP, and collaboration with cross-functional teams in a global healthcare environment.

Ideal candidates will have strong experience with LC–MS/HPLC, data analysis, and report writing, plus excellent communication skills to support study interpretation and

Qualifications

• Bachelor's degree or higher with relevant experience in quantitative bioanalysis.
• Knowledge of GLP regulations and good documentation practices.
• Ability to read and interpret complex technical documents.

Responsibilities

• Set up, operate, and troubleshoot analytical equipment, such as Mass Spectrometers and/or HPLCs for laboratory operation.
• Develop and validate analytical methods to quantify drugs and metabolites in biological matrices to support bioequivalence and other pharmacokinetics studies with supervision.
• Document laboratory activity in accordance with established procedures.
• Review and write reports.
• Assist in troubleshooting analytical problems encountered during study runs.
• Serve as a scientific/technical information resource for junior laboratory staff.
• Review data and associated documentation for scientific soundness and compliance with Standard Operating Procedures.
• Write and revise analytical methods Perform other duties as assigned.

Skills

Mass spectrometry

HPLC

Bioanalysis

GLP

Data analysis

Report writing

Communication

Instrument software

Education

Bachelor's degree

Doctorate

Master's degree

Tools

HPLC

Mass Spectrometry

Laboratory automation

Data acquisition software

Job description

Viatris is seeking a Scientist to set up and operate analytical equipment, develop and validate methods, and ensure accurate documentation for bioequivalence and PK studies. The role emphasizes quality data generation, compliance with GLP, and collaboration with cross-functional teams in a global healthcare environment.

Ideal candidates will have strong experience with LC–MS/HPLC, data analysis, and report writing, plus excellent communication skills to support study interpretation and