Scientist III Method Development – Bioanalytical Programs

B2S Life Sciences LLC•Franklin, IN

6d•Onsite

About The Position

The Scientist III Method Development is a key member of the Bioanalytical Assay Development and Validation team. This team has overall responsibility for the development, optimization, pre-study validation and in-study execution of bioanalytical methods to support clients’ programs for the development of biotherapeutic drug candidates. Most often this work is performed using critical reagents generated by B2S Life Sciences. The range of bioanalytical support includes early phase ADME investigations, reagent optimization, generation of optimal matched pair of antibodies, method qualification, and non-GLP & GLP sample analysis. The individual in this role will help ensure B2S bioanalytical assays are engineered appropriately to ensure quality and regulatory standards for Good Laboratory Practice (GLP) compliance are followed. Scientist III designs and executes experiments, with minimal supervision, which complement the company's capabilities in custom critical reagents to enable clients to efficiently make data-driven decisions for optimal analytical outcomes to support biotherapeutic drug development. The individuals will have the ability to work independently with little or no supervision with a focus on bioanalytical science and capable of troubleshooting assay issues efficiently. In addition the individual will have the ability to work across different therapeutic areas to manage multiple projects concurrently.

Requirements

Bachelor’s Degree (B.S./B.A) or Master’s Degree (M.S.) in a related science with at least four-years of direct laboratory experience
Doctorate Degree (P.H. D.) in biology or related degree with zero to two years of direct laboratory experience.
An equivalent combination of related education and required work experience will be considered.
Laboratory experience in developing and troubleshooting LBAs and cell culture bioassays is desired.
Experience in a good laboratory practice (GLP) and good clinical practice (GCP) environment is desired.
Experience with biotherapeutic bioanalysis at a contract research organization (CRO) is desired.
The ability to adapt and conform to shifting priorities and demands and execute accordingly.
Strong organizational and communication skills, both written and verbal.
The position may require evening and weekend work, domestic travel, and a valid driver’s license.
Computer software skills required, including Microsoft Office Suites.
Individuals must be able to perform each essential duty according to the requirements of the Organization.
The requirements listed above are representative of the knowledge, skills, and/or abilities required.
Competencies: Quality and Quantity – Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality; Meets productivity standards; Completes work in timely manner; Strives to increase productivity; Works quickly but efficiently.
Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs workflows and procedures.
Safety and Security – Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly.
Problem Solving – Identifies and resolves problems in timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics.
Oral and Written Communication – Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Responds well to questions; Demonstrates group presentation skills; Participates in meetings; Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Reads with the ability to interpret written information.
Other Skills and Abilities: Ability to adapt and conform to shifting priorities and demands and execute accordingly.
Strong organizational and communication skills, both written and verbal.
Computer software skills required include Microsoft Office Suite: Outlook, Word, Excel, PowerPoint, OneDrive, OneNote, SharePoint, and Teams.

Nice To Haves

Laboratory experience in developing and troubleshooting LBAs and cell culture bioassays
Experience in a good laboratory practice (GLP) and good clinical practice (GCP) environment
Experience with biotherapeutic bioanalysis at a contract research organization (CRO)

Responsibilities

Plan, execute, troubleshoot and analyze experiments and interpret scientific findings.
Troubleshoot existing analytical methods.
Work independently in a collaborative team environment
Compile scientific data (including analysis and technical writing)
Record and note the experimental processes.
Report and treat data with prominent level of integrity and ethics.
Possess good oral communication and willing to communicate frequently with clients
Comply with application able regulations (GXP)
Maintain proper records in accordance with standard operating procedures (SOPs) and policies.
Dedicated to bioanalytical science and work to grow expertise to maintain current knowledge with respect to industry and regulatory trends.
Design and perform scientific experiments with a pre-defined goal including developing new methodologies, protocols, and/or test procedures that contribute to core group research goals.
Seek bioanalytical solutions that are innovative yet simple to execute.
Willing to publish work in scientific journals and make presentations at meetings.
Maintain laboratory equipment, as needed.
Develop new methodologies, protocols, and/or test procedures that contribute to core group research goals and reflect expert knowledge.
Willingness to mentor junior staff and team members
Maintains laboratory equipment, as needed.
Performs other duties as assigned.