Scientist - II

Join the Global Preclinical Development group as a Senior Bioanalytical Scientist within a high-performing Good Laboratory Practices (GLP) laboratory. This role is designed for a highly motivated bench scientist who thrives in a hands-on environment, focusing on the development and implementation of critical bioanalytical assays. You will serve as a technical lead within the Bioanalytical group, overseeing project responsibilities and establishing new capabilities to support drug safety and metabolism studies. This is an ideal opportunity for an expert in ligand binding assays (LBA) to work independently while contributing to a collaborative, cross-functional team dedicated to accelerating preclinical drug development.

Responsibilities

• Independently develop, optimize, and troubleshoot Ligand Binding Assay (LBA) methods with a focus on high quality and operational efficiency.
• Perform proficient, independent implementation of LBA for biological sample analysis, including sample preparation, instrument setup, and data interpretation.
• Establish and expand LBA capabilities within the team, including equipment procurement and the design of laboratory workflows.
• Author comprehensive bioanalytical methods and technical reports for both sample analysis and validation studies.
• Ensure all laboratory documentation is recorded in real-time, maintaining strict accuracy and compliance with GLP and departmental guidelines.
• Assemble critical documentation packages for regulatory submissions and maintain adherence to company SOPs and safety protocols.
• Manage project timelines and short-term goals independently with minimal management oversight.
• Interface effectively with internal partners across functional lines, including Quality Assurance, Drug Safety, and Program Management.
• Utilize LIMS (Watson) and other data management systems to process and track experimental results.
• Balance multiple complex tasks simultaneously while maintaining a collaborative "team player" approach to laboratory operations.

Education

• Ph.D. in Chemistry, Biochemistry, or a related scientific discipline with at least 3 years of industrial experience.
• Alternatively, a Master of Science (M.S.) in Chemistry, Biochemistry, or a related discipline with a minimum of 7 years of industrial experience.

Experience

• Extensive experience in developing, validating, and implementing ligand binding assays (LBA) specifically under GLP regulations.
• Proven proficiency in using Watson LIMS or similar laboratory information management systems.
• Strong background in a bioanalytical laboratory environment is highly preferred.
• Experience with LC-MS/MS assays is a significant plus.
• Advanced proficiency with Microsoft Office products for data reporting and communication.

Additional Information

• Skills: Excellent written and verbal communication skills are required for interacting with external partners and regulatory documentation.
• Attributes: Seeking a self-starter with a strong aspiration for continuous professional development and the ability to work with high autonomy.