LCMS Method Development Scientist II/III

Pharmaron; Exton (PA); On-site; USD 65,000 - 85,000; Full time

Job summary

Pharmaron in Exton, PA is seeking a Scientist II/III, LCMS Method Development to advance bioanalytical method development and validation across multiple modalities.

The role focuses on developing LC-MS/MS and HPLC methods, supporting GLP-regulated studies, and contributing to regulatory documentation within a collaborative team.

Ideal candidates will have a pharmaceutical sciences background, experience with bioanalysis, and the ability to work in a fast-paced, client-focused CRO environment.

Qualifications

• Bachelor's degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or related field.
• Scientist II: 2+ years of bioanalytical testing experience; Scientist III: 4+ years.
• Experience with development and GLP-regulated bioanalytical studies.
• Strong understanding of HPLC and LC-MS/MS methodologies.
• Excellent analytical thinking, troubleshooting, and organizational skills.
• Ability to thrive in a fast-paced, collaborative, and matrixed environment.

Responsibilities

• Develop, validate, and troubleshoot LC-MS/MS bioanalytical methods.
• Design studies to meet sponsor and internal goals.
• Support bioanalytical testing for DMPK and regulated studies.
• Perform sample analysis using HPLC and LC-MS/MS per GLP.
• Review study protocols and report data.
• Author validation reports, summaries, and study reports.
• Support regulatory submissions with scientific documentation.
• Collaborate with teams and clients to ensure project success.
• Identify and resolve technical challenges, drive improvements.
• Participate in project reviews and compliance initiatives.

Skills

Analytical thinking

Troubleshooting

Organizational skills

Teamwork

Bioanalytical testing

LC-MS/MS

HPLC

Education

Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or related field

Tools

LC-MS/MS

HPLC

Job description

Pharmaron in Exton, PA is seeking a Scientist II/III, LCMS Method Development to advance bioanalytical method development and validation across multiple modalities.

The role focuses on developing LC-MS/MS and HPLC methods, supporting GLP-regulated studies, and contributing to regulatory documentation within a collaborative team.

Ideal candidates will have a pharmaceutical sciences background, experience with bioanalysis, and the ability to work in a fast-paced, client-focused CRO environment.