Method Development Scientist II

Job Responsibilities

• Support the development, transfer, troubleshooting, and documentation of sensitive and reliable LC-MS/MS bioanalytical methods for the analysis of pharmaceuticals and related compounds in biological matrices.
• Apply scientific principles, regulatory awareness, and hands-on laboratory expertise to generate high-quality data and support internal and external communications.
• Contribute to process improvements by supporting method development and method transfer activities, including method writing and associated laboratory work.
• Support troubleshooting across development, validation, and sample analysis.
• Maintain complete, accurate, and timely documentation in accordance with SOPs, GLP, and regulatory requirements.
• Communicate method performance, risks, and resource needs to support data-driven decision-making.
• Serve as a technical resource within the group, assisting with troubleshooting and training as appropriate.
• Participate in client interactions and internal cross-functional collaborations.
• Contribute to the evaluation of departmental procedures and local process improvements.
• Promote a cohesive and collaborative team environment.

Minimum Requirements

• Bachelor’s degree (Chemistry, Biochemistry, etc.)
• 5 years or more of analytical laboratory experience
• 5 years or more of LC-MS/MS experience

Preferred Requirements

• Doctoral degree (Chemistry, Biochemistry, etc.)
• With any lab experience
• Any version of GLP/GMP/GCP/SOP experience helpful
• Method development exposure

Additional Requirements

• Demonstrated communication skills (external publications and presentations)
• Client management experience
• Proven ability to prioritize and manage time
• Excellent attention to detail

Benefits

• Medical
• Dental
• Vision
• Life
• STD/LTD
• 401(k)
• Paid Time Off (PTO) or Flexible Time Off (FTO)
• Tuition Reimbursement
• Employee Stock Purchase Plan