Research Scientist

QPS • Newark, DE

4d • Onsite

About The Position

QPS, LLC is hiring a Research Scientist in its Bioanalytical (GBA) department to support the expansion of bioanalytical capabilities for drug development. GBA includes Small Molecules, Proteins, and Oligonucleotides laboratory units, each with method development, method validation, and sample analysis groups. The department quantifies small molecules, peptides, proteins, oligonucleotides, and biomarkers using chromatographic techniques coupled with tandem mass spectrometry.

For the Sample Analysis group, the Research Scientist serves as a Principal Investigator (PI) on bioanalytical studies and manages studies, interprets and reports data, and participates in method validation as needed. The PI also works with clients to establish assay requirements and intended use, then develops assays using appropriate technology platforms. The role is based 100% at a QPS office or facility in Newark, Delaware.

Requirements

• Advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or a related scientific discipline.
• Recent graduates must have direct experience with LC-MS/MS analysis.
• Candidates more than two years past graduation must have direct experience developing bioanalytical assays using LC-MS/MS.
• Understanding of experimental design and planning, and data collection and analysis software.

Nice To Haves

• CRO experience, particularly for candidates more than two years past graduation.

Responsibilities

• Independently manage multiple sample analysis projects or one or more method development or validation studies with minimal supervision.
• Prepare, review, and understand study protocols.
• Coordinate with clients and internal resources to plan, design, and conduct studies.
• Evaluate data significance and report findings.
• Prepare study summaries and reports.
• Set up, use, and maintain complex instrumentation.
• Communicate project timelines, status, data, reports, and inquiries to clients and study sites, and address issues as they arise.
• Maintain appropriate regulatory compliance for each study, prepare QA-related documents, and address QA audit findings.
• Maintain project schedules and timelines.
• Supervise, train, and mentor junior scientific staff.
• Develop, validate, and run sensitive, reliable, and efficient LC/MS/MS assays for TK/PK assessment.
• Ensure GLP regulations and SOPs are followed in bioanalytical service activities.
• Work with clients to identify assay requirements and intended use and develop assays using appropriate technology platforms.

Benefits

• Company-matched 401(k).
• Company-sponsored Group Life/AD&D insurance.
• Short- and long-term disability insurance.
• Training and learning opportunities.
• Structured career ladders and advancement opportunities.
• Bonuses and merit increases linked to individual, team, and company performance.
• Internal committees focused on employee needs and enjoyment.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level