Scientist II/III, LCMS Method Development (Bioanalysis)

Position: Scientist II/III, LCMS Method Development (Bioanalysis) Salary Range: $65,000-$85,000 Location: Exton, PA (On-site) Job Overview Pharmaron is seeking a Scientist II/III, LCMS Method Development (Bioanalysis) to join our growing Bioanalytical Sciences team in Exton, PA. In this role, you will contribute to the development and validation of innovative bioanalytical methods supporting drug discovery and development programs across a diverse range of therapeutic modalities, including small molecules, peptides, oligonucleotides, PROTACs, biologics, and emerging therapies. Key Responsibilities Independently develop, optimize, validate, and troubleshoot LC-MS/MS bioanalytical methods. Design scientifically sound studies that meet sponsor and internal objectives. Execute and support bioanalytical testing for DMPK and regulated studies. Perform sample analysis using HPLC and LC-MS/MS platforms in compliance with developmental and GLP requirements. Review and execute study protocols governing bioanalytical studies and sample analysis. Process, analyze, interpret, and report study data. Author protocols, validation reports, technical summaries, and study reports. Support regulatory submissions through high-quality scientific documentation. Serve as Principal Investigator (PI) and/or Study Director (SD) within areas of expertise. Actively identify and resolve technical challenges while driving continuous improvement. Collaborate with scientists, project teams, management, business development, and clients to ensure successful project execution. Participate in project review meetings and compliance-related initiatives. What We’re Looking For Bachelor's degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or a related scientific discipline. Scientist II: Minimum 2 years of bioanalytical testing experience. Scientist III: Minimum 4 years of bioanalytical testing experience. Experience supporting development and/or 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. Preferred Qualifications Experience with LC-MS/MS method development and validation. Experience analyzing peptides, oligonucleotides, PROTACs, and complex biologics. Familiarity with DMPK studies and regulated bioanalysis. Experience authoring scientific reports and supporting regulatory submissions. Prior CRO, pharmaceutical, or biotechnology industry experience. Experience serving in client-facing scientific roles. Benefits Insurance including Medical, Dental & Vision with significant employer contributions. Employer-funded Health Reimbursement Account. Healthcare & Dependent Care Flexible Spending Accounts. 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance. 401(k) plan with generous employer match. Access to an Employee Assistance Program. Pharmaron is proud to be an Equal Employment Opportunity and affirmative action employer. #J-18808-Ljbffr Pharmaron