Bureau Veritas North America · 4 days ago
Biologist I
Bureau Veritas North America is a leading company in consumer product services, and they are seeking an Analyst I to support clinical trial sample analysis. The Biologist will be responsible for organizing, preparing, and analyzing samples while ensuring compliance with regulatory standards and maintaining accurate documentation.
Information ServicesMedia and EntertainmentPublic Safety
Responsibilities
Support the implementation of immunogenicity assays and biomarker assays by collaborating with internal scientific/regulatory/quality/clinician subject matter experts (SMEs)
Perform experiments to implement assays and analyze samples
Draft, compile, and/or review data, protocols and reports
Aid in troubleshooting assay issues
Ensure assays and analyses comply with most current regulatory agency guidance
Manage multiple assay projects and meet timelines established by customers
General laboratory techniques including, but not limited to, pipetting, weighing, and buffer preparation
Familiarity with or willingness to work with automation (liquid handlers, automated Western systems, tube labelers)
Data processing (familiarity with Excel and other graphing software) and accurately recording lab activities in an electronic notebook
General laboratory services (inventory, supplies, cleaning, stocking, instrument care and maintenance, and reagent or sample handling)
Follow the guidelines set forth with clients and Company Quality, Health, Safety, Security and Environmental policies and procedures
Comply with clients’ and Company management systems in accordance with appropriate regulatory agencies
Perform other essential tasks, projects, and responsibilities as required
Other duties as defined by Manager, department needs and workload
Qualification
Required
Bachelor's Degree in science or a related discipline
Self-regulated with high attention to detail for quality and strong organization skills
Ability to understand and execute multi-step protocols
Experience with laboratory documentation practices: recording of information and details necessary to recreate experiment as well as notation of any deviations or errors
Proven Microsoft Word, Excel, Teams, SharePoint, and PowerPoint skills
Strong attention to detail and ability to multi-task
Ability to understand the objective of experiments in order to identify issues
Excellent communication skills - verbal and written. Ability to communicate issues as they occur
Works well both as a team and as an individual contributor
Strong safety focus and willingness to assist with general lab housekeeping
Ability and willingness to adapt to changing project needs and timelines and flex plans and responsibilities as needed
Adheres to company values
Ability to pass Assay Competency Testing in accordance with regulatory requirements in order to maintain employment
Preferred
Experience in a highly detail-oriented laboratory environment
ELISA and liquid handling experience
Experimental design; scientific approach to problem solving; method development, optimization, and validation
Experience in a regulated (for example, Good Laboratory Practices [GLP], Good Clinical Practices [GCP], Good Manufacturing Practices [GMP]) environment
Company
Bureau Veritas North America
Bureau Veritas is a global leader in the Quality Assurance, Health, Safety & Environmental (QHSE), and Social Responsibility industries.
H1B Sponsorship
Bureau Veritas North America has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (3)
2024 (3)
2023 (7)
2022 (6)
2021 (3)
2020 (6)
Funding
Current Stage
Late StageCompany data provided by crunchbase