Sr. Staff Scientist - AST

Sr Staff Scientist - AST Act as technical and scientific expert in the design and development of high-quality products on time, within budget, and with a high degree of customer satisfaction. Acts as an expert for new product development or current product improvement projects. Acts as an expert for AST investigations. Primary Duties Lead VITEK 2 AST drug round development projects. Participate in VITEK 2 AST investigations. Collaborate closely with the software, hardware development and system engineering teams. Contribute to the development of tools for analyzing large performance data sets generated from (AST/ID/molecular) experiments. Acts as expert for all biological testing needed for assay development and system verification activities. Troubleshoot technical issues specific to the (AST/ID/Molecular Biology) tests/system, record and report these issues cross‑functionally, and provide suggestions and resolutions for investigations. Lead other scientists and managers to optimize testing protocols and workflows within the lab. Maintain accurate records of experiments and results, write work instructions (WIs), standard operating procedures (SOPs), protocols, reports, process flows etc. Ensure compliance with regulatory standards (e.g., FDA, ISO) and comply with biohazard safety standards. Participate in product risk assessment, technical design reviews and critically evaluate design and implementation plans, can act independent reviewer. Summarize findings and present results to cross‑functional teams. Mentor and train new and existing team members and be a technical advisor for data analysis problems. Act as SME for audits, interaction with FDA and other authorities, and key opinion leaders. Perform all work in compliance with company quality procedures and standards. Perform other duties as assigned. Qualifications Required Education, Training and Experience Bachelor's degree required in Medical Technology, Life Sciences, Biomedical, Microbiology, or related science field. Education Substitution: In lieu of a bachelor's degree, 4 years of additional relevant experience, defined below, will be accepted. 10+ years of professional related experience with VITEK 2 drug development (including CLSI reference methods) and participation in VITEK 2 AST investigations. Preferred Education, Training and Experience Advanced degree (MS, PhD) preferred. Experience in product development in regulated environment. Advanced skills necessary for good laboratory safety, aseptic technique, and basic Microbiology/Molecular technique. Knowledge, Skills, and Abilities (KSAs) Consistently upholds and reflects the core ethical principles and values that bioMerieux promotes. Comfortable giving clear, direct, and actionable feedback. Demonstrates assertiveness and confidence in the face of a challenge. Written Communications - including the ability to communicate technical data in written form. Informing others by sharing clear, timely information to ensure alignment. Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time. Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel. Supervisory Responsibilities No direct or indirect supervisory responsibilities. Makes operational and tactical decisions with short‑term impact and strategic decisions with long‑term impact, both with little to no supervisory review. Working Conditions & Physical Requirements (Summary) Ability to remain in a stationary position for prolonged periods. Ability to ascend/descend stairs, ladders, ramps, and similar structures. Ability to wear PPE correctly most of the day. No operation of heavy machinery required. No requirement to move objects up to 50 pounds. Domestic travel: 5%. International travel: 5%. Total travel: 10%. Position is lab‑based and follows work practices for working with laboratory biohazards and chemical hazards. Salary & Benefits The estimated salary range for this role is between $140,000-$180,000. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux's bonus program. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer. In addition, bioMerieux offers a competitive Total Rewards package that may include: A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options. Company‑Provided Life and Accidental Death Insurance. Short and Long‑Term Disability Insurance. Retirement Plan including a generous non‑discretionary employer contribution and employer match. Adoption Assistance. Wellness Programs. Employee Assistance Program. Commuter Benefits. Various voluntary benefit offerings. Discount programs. Parental leaves. Equal Employment Opportunity Statement BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at View phone number on click.appcast.io, by email at View email address on click.appcast.io, or by dialing 711 for access to Telecommunications Relay Services (TRS). #J-18808-Ljbffr bioMerieux Inc.