Duration: 10 months contract Shift: Monday–Friday, approximately 8:00 AM–5:00 PM
Job Description:
The ideal candidate is a hands-on bioanalytical Scientist with strong large-molecule experience and demonstrated expertise in ligand-binding assays, particularly ELISA and/or ECL, including method development and validation.
The candidate should have experience working in a GxP-regulated pharmaceutical, biotechnology, or CRO laboratory and bring strong documentation, data analysis, critical-thinking, and problem-solving skills.
The strongest candidates will be collaborative, detail-oriented, adaptable, quick learners who can successfully multitask in a dynamic laboratory environment, independently manage their scientific responsibilities, and provide appropriate experimental guidance to junior analysts.
Candidates with solely LC-MS experience and no ligand-binding assay background are not the target profile.
The Pharmacokinetics, Drug Metabolism & Bioanalytical (PKDM-BA) organization is dedicated to advancing the discovery and development of innovative, safe, and effective medicines.
Scientists within PKDM-BA collaborate closely with cross-functional partners, including protein therapeutics, medicinal chemistry, pharmacology, toxicology, pharmaceutical sciences, clinical pharmacology, and regulatory affairs.
Together, they support the identification of promising therapeutic candidates, preclinical development, clinical evaluation, and regulatory submissions.
We are seeking a highly motivated scientist to develop, validate, and implement robust bioanalytical methods for quantifying large-molecule biotherapeutics.
These methods will support both nonclinical and clinical research programs.
Key Responsibilities:
Participate in the execution of experiments to support development, validation, and implementation of bioanalytical methods for large-molecule therapeutics, including oligonucleotides, in clinical and nonclinical samples.
Contribute to protocol optimization, troubleshooting, and assay improvement activities to support robust, reliable, and transferable bioanalytical methods.
Collaborate with cross-functional partners to support non-clinical and clinical bioanalytical needs across drug development programs.
Preferred Qualifications:
4+ years of laboratory experience.
Experience in immunology, immunochemistry, biochemistry, cell biology, or related disciplines.
Working knowledge of GxP regulations and bioanalytical requirements in drug development.
Strong critical thinking and problem-solving skills, with the ability to integrate complex data to advance drug discovery and development programs.
Proven ability to communicate scientific concepts effectively to audiences with varying levels of technical expertise.
Demonstrated commitment to scientific excellence and innovation.
Track record of contributing as a lead author on peer-reviewed publications.
Must Have Skill Sets:
Immunoassay knowledge
Working knowledge of GxP regulations
project management skills
About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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