Biologist IV

Bureau Veritas•Indianapolis, IN

23d•$31 - $35•Onsite

About The Position

The Biologist IV - ClinPath will develop target related clinical pathology (hematology, clinical chemistry, urinalysis, and immunology) testing and biomarker endpoints in early development systems. The Biologist IV – ClinPath will assist with ELISA immunoassays and associated automation.Duties and Responsibilities:It is everyone’s responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress..

Requirements

Proficiency with Cobas chemistry systems (602, C502/ISE)
Proficiency with Advia and Sysmex hematology instruments
Proficiency in preparation of slides/blood smears and reading and interpreting them
Proficiency with immunoassay method development and validation procedures
Proficiency in dilution schemes
Familiarity working with automation (e.g. Hamilton, Tecan)
Professional, clear and concise communication required in both written and verbal formats
Proven Microsoft Word, Excel, Teams, SharePoint, and PowerPoint skills
Ability to quickly learn and understand job-specific software
Ability to understand basic scientific terminology and communicate it to others
Team-oriented and the ability to work in a collaborative environment
Strong interpersonal skills – approachable, relationship building, with external and internal contacts, demonstrating initiative and adaptability.
Ability to oversee large projects
Be a proven multi-tasker that truly thrives on juggling multiple projects in a deadline driven environment
Possess strong organizational skills with ability to quickly assess project status and communicate it effectively
Driven, energetic person able to coordinate activities among different areas of the department
Strong leadership skills
Champion company values including team engagement
Degree requirement: Bachelor's Degree in biology or medical technology
Minimum of Two(2) years of experience with routine hematology, urine chemistry, clinical chemistry panel testing early development systems
Minimum of two (2) years of experience in highly detail-oriented environment

Responsibilities

Performs early development Clinical Pathology Assays – Maintenance and use of hematology automated analyzer for whole blood analysis and maintenance and use of clinical chemistry analyzers for analysis of serum, urine, and other body fluids. Performs blood and bone marrow smears and reviews the slides.
Maintain notebooks, prepare and present data and use computer software LIMS, Excel or other data visualization tools to organize, analyze and summarize data.
Develop and characterize new biomarker assays or disease models to support clinical drug development. Evaluate new technologies that relate to biomarker development.
Develop and perform assays in proteomics biomarkers and molecular biology techniques such as ELISA
Track and manage workflow, assay requests and metrics using laboratory processes and systems.
Perform Instrument maintenance, troubleshooting and qualification of instruments
Understand and adhere to standards for appropriate test methods and SOP’s.
Prepare a variety of samples for testing using prescribed testing methods, following testing standards / specifications.
Perform quality and safety checks on samples submitted prior to testing.
Conduct testing on a variety of samples using prescribed testing methods, following testing standards / specifications appropriate to the sample. Prepare dilutions.
Able to troubleshoot with N+1 for any client issues or questions with the aim of enhancing client satisfaction and improving client relations.
Accurately report and record test data in electronic notebook or handwritten notebooks as needed in a timely manner
Prepare a variety of equipment for testing using prescribed standards / specifications
Maintain supplies, lab cleanliness and analytical instrumentation, as required.
Prepare stock solutions, and keeping shelves and reagent stocked.
Maintain up to date knowledge of current methods and products to be tested.
Work with biological tissue specimens from animals and people
Track storage and log of pre-clinical and clinical samples as well as exploratory research samples
Follow the guidelines set forth with clients and in the Bureau Veritas Consumer Products Services, Inc Quality, Health, Safety, Security and Environmental policies and procedures.
Comply with clients and Bureau Veritas Consumer Products Services, Inc management systems in accordance with appropriate regulatory agencies.
Adhere to the requirements of the BV-CPS Quality System.
Other duties as defined by Manager, department needs and workload.