Full-Time

Principal Business Development Manager

Bioanalytical Solutions

Deadline 4/14/27
Waters

Waters

10,001+ employees

High-performance analytical instruments, software, and services

No salary listed

San Francisco Bay Area, CA, USA

Remote

Remote within the United States, with preference for candidates on the West Coast; travel up to 50% is required.

Bachelor's, Master's, MBA, PhD

Category
Sales & Account Management (1)
Required Skills
Microsoft Office
Sales
Lead Generation
Forecasting
CRM
Salesforce
Marketing
Business Analytics
Data Analysis

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Requirements
  • A bachelor's degree in a life science-related field is required.
  • A minimum of 5 years of sales or business development experience serving academic, government, or pharmaceutical scientific markets is required.
  • The candidate must be able to assess research needs and translate them into effective commercial strategies.
  • Proficiency with Salesforce customer relationship management, business analytics tools for pipeline management, forecasting and account planning, and Microsoft Office is required.
  • The candidate must be able to identify, target, and engage high-value research institutions and pharmaceutical discovery customers.
  • The candidate must be able to develop marketing strategies tailored to academic research cycles and organizational structures.
  • The candidate must be able to build long-term relationships across universities, core facilities, research institutes, and pharmaceutical discovery laboratories.
  • The candidate must have strong analytical skills for interpreting scientific trends, grant funding patterns, and organizational priorities.
  • The candidate must have effective negotiation skills for instrument sales, multi-group purchases, and service or workflow agreements.
  • The candidate must have strong written and verbal communication skills and be able to present complex scientific solutions clearly.
  • The candidate must be able to motivate and influence cross-functional teams.
  • The candidate must have a deep understanding of liquid chromatography, mass spectrometry, and flow cytometry as applied to academic, pharmaceutical discovery, and translational research.
  • The candidate must be able to communicate research applications, workflow integration, and value propositions to diverse scientific audiences.
  • The candidate must be willing to travel up to 50% for campus visits, seminars, conferences, customer meetings, and team activities.
Responsibilities
  • Identify and pursue new business opportunities across academic departments, shared resource facilities, government laboratories, and pharmaceutical research organizations.
  • Generate and qualify leads through scientific networking, campus visits, conferences, workshops, and digital outreach.
  • Develop and execute strategies to broaden adoption of bioanalytical technologies in research-intensive organizations.
  • Maintain an accurate sales pipeline and provide reliable forecasting for the target customer segment.
  • Collaborate with regional sales and marketing teams to convert academic and research opportunities into orders.
  • Support the sales process through technical presentations, workflow discussions, demonstrations, and proposal and quote negotiation.
  • Develop and implement sales plans tailored to academic funding cycles, grant landscapes, and institutional priorities.
  • Set and monitor performance targets to ensure goals aligned with the Annual Operating Plan are achieved or exceeded.
  • Deliver remote and in-person training for sales and marketing teams focused on academic bioanalytical workflows, research applications, and adoption drivers.
  • Provide tools, content, and positioning strategies for academic and government research environments.
  • Use virtual platforms, academic seminar programs, webinars, and outreach events to expand awareness and build the funnel in academic and pharmaceutical discovery markets.
  • Create and execute promotional initiatives aligned with academic research trends and institutional needs.
  • Build and maintain relationships with principal investigators, laboratory managers, core directors, and research administration.
  • Collect and communicate customer insights, research challenges, and success stories to guide commercial strategy.
  • Ensure customer service that supports recurring business and long-term partnerships.
  • Provide regular updates on performance, market dynamics, grant trends, and customer feedback to the Pharma Program Lead.
  • Use data-driven insights to adjust strategies and maximize success in the target customer segment.
  • Maintain working knowledge of quantitative and qualitative liquid chromatography-mass spectrometry, flow cytometry, and complementary analytical technologies.
  • Communicate technical and workflow advantages effectively to scientific audiences with varying levels of expertise.
  • Capture feedback from researchers, core facility staff, and field sales teams to support refinement of bioanalytical solutions.
  • Partner with sales, marketing, product management, and the broader Analytical Science business segment to deliver research-focused solutions.
  • Report directly to the Pharma Lead within the LCMS Business Segment in the Analytical Sciences Division.
Desired Qualifications
  • An MBA or a master's degree or PhD in a scientific discipline is highly advantageous.
  • The candidate should be a creative self-starter who can design and execute impactful customer engagement programs.

Waters provides analytical system solutions, software, and services for scientists across biopharma, clinical research, forensics, life science, food and beverage, and environmental sectors. Its products include high-performance instruments such as the BioAccord System, along with optimized software and support services that enable precise and reproducible analytical results. The company differentiates itself by offering end-to-end, integrated hardware, software, and services across a broad range of markets, with a strong emphasis on reproducibility, data insights, and comprehensive customer support. Its goal is to unlock the potential of science by solving critical problems that matter to human health and well-being.

Company Size

10,001+

Company Stage

IPO

Headquarters

Milford, Connecticut

Founded

1958

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue reached $1.645 billion; management raised 2026 organic growth to 7%-9%.
  • GLP-1 testing grew over 40% in Q2 2026, supporting recurring assay demand.
  • ADLM 2026 and September 3 workflow messaging show customers buying integrated lab systems.

What critics are saying

  • The February 2026 BDS deal adds $12.96 billion integration risk and execution drag.
  • Q2 2026 included a 3% workforce cut and $52 million restructuring charges.
  • If Waters misexecutes diagnostics integration, SCIEX and Roche will steal clinical LC-MS/MS workflows.

What makes Waters unique

  • Waters owns regulated LC-MS/MS workflows, from instruments through informatics and consumables.
  • The February 9, 2026 BD Biosciences and Diagnostics combination broadened its diagnostics moat.
  • July 27, 2026 Xevo TQ Absolute XR IVD claims five-times sensitivity and six-times robustness.

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Benefits

Hybrid Work Options

Growth & Insights and Company News

Headcount

6 month growth

16%

1 year growth

16%

2 year growth

14%
MarketScale
Sep 3rd, 2026
Lab automation ROI hinges on integration, not instrument sensitivity claims.

Lab automation ROI hinges on integration, not instrument sensitivity claims. At ADLM 2026, Waters and LabCollector delivered a clear message for lab leaders: the limiting factor in automation is often integration, not hardware. Waters introduced the Xevo TQ Absolute XR IVD mass spectrometer and is positioning it at "5x greater sensitivity" versus in-class instruments, according to SelectScience, but that advantage only carries through if sample prep, calibration and QA, middleware rules, and LIMS result review can keep pace. In parallel, LabCollector announced an AI Co-Scientist feature set for natural-language search, knowledge retrieval, and AI-assisted content creation inside ELN and LIMS workflows, also reported by SelectScience, shifting attention from pipetting speed to retrieval, approval, permissions, and versioning in systems that sit on the documentation path. The Scientist's overview of semi-automated versus fully automated approaches reinforces the point: labs can automate in modules, but they have to run automation as one system. This story was produced through MarketScale. See how Sciences teams put it to work with Executive Thought Leadership. By MarketScale Newsroom · September 3, 2026, 5:37 AM PDT · Lab Automation Clinical Laboratory Lims Eln Learn this in 60 seconds Key facts, context, and what it means, in one minute. Key takeaways The bottleneck in automation is often the handoff, instrument to middleware to LIMS, so sensitivity and throughput gains depend on interfaces and downstream review as much as the instrument spec. Waters' "5x greater sensitivity" positioning and LabCollector's AI Co-Scientist both point to integration work, sample prep, calibration and QA, middleware rules, and LIMS result review, as the gating factor for ROI. As ELN/LIMS add conversational search and AI-assisted content creation, speed gains move from pipetting to retrieval, approval, permissions, and versioning inside systems that sit in regulated or audited workflows. Get featured Want to get featured in MarketScale Sciences? Create a free MarketScale workspace and get your company's expertise featured across our Sciences coverage. No credit card, no demo required. The new bottleneck in lab automation is often the handoff, instrument to middleware to LIMS, not the robot arm. Waters introduced the Xevo TQ Absolute XR IVD mass spectrometer at ADLM 2026, and SelectScience reported the company is positioning it at "5x greater sensitivity" versus in-class instruments. That kind of headline spec only matters if the lab's workflow can preserve it, sample prep, calibration and QA, middleware rules, and LIMS result review. ADLM 2026 is putting performance claims back on the table, but the workflow owns the outcome. SelectScience's ADLM coverage also highlighted Roche's view that automation, standardization, and core-lab integration are key to expanding access to mass spectrometry-based testing, framed around making LC-MS/MS more routine rather than more "expert-only." For clinical lab directors and health system procurement teams, the question is whether the lab's full chain of custody can preserve any sensitivity advantage through to the LIS/LIMS result. Sample prep and collection volume constraints, calibration and QA, pre-analytical variability, instrument scheduling, middleware rules, and downstream data review time can all eat the gain. Sensitivity claims still matter for acceptance testing and method validation, but they force an integration decision. If the install plan does not include the interfaces and the SOP rewrites, the "5x" lives on a slide. ELN and LIMS are becoming the control plane for automation. LabCollector's AI Co-Scientist announcement is a different kind of automation news: it is about compressing the time between a question and an actionable answer inside the systems where labs already document work. SelectScience reported the feature set is designed for conversational interaction with laboratory knowledge and for generating scientific content directly within LabCollector's ELN and LIMS workflows. Automation ROI is increasingly limited by retrieval and approval inside ELN and LIMS systems, not only by pipetting speed. When staff can pull prior protocols, reagent history, instrument notes, or the last deviation resolution without digging through folders and PDFs, cycle time can drop even if the physical workflow stays semi-automated. In regulated or audited environments, AI-assisted text generation inside an ELN puts permissions, review, and versioning in the critical path. Labs will need to decide where generated content is allowed, how it is flagged and reviewed, and how it is version-controlled in the audit trail, because the ELN is where procedures and results live. Semi-automation still wins on adoption speed, and the gap shows up in integration work. The Scientist's explainer on lab automation lays out why semi-automated workflows remain common: cost, equipment availability, and the need to tailor automation to application-specific requirements. The article describes how labs often automate a single repetitive task with liquid handling while keeping complex steps manual, an approach that saves time and reduces error without demanding a fully hands-off line. That adoption path is still the default in many organizations, and it intersects with the 2026 product news in a useful way. If the lab is going to stay semi-automated for the next budget cycle, the most durable investments are often the ones that reduce friction at the seams: standardized naming, barcoding discipline, instrument connectivity, and LIMS configuration that can absorb new assays and new instruments without a replatform. SelectScience's product news on Beckman Coulter's DxI 9000 Immunoassay Analyzer points in the same direction. The company said it is expanding infectious disease serology on DxI 9000 to support earlier detection through sensitive and efficient serology testing. The release is light on chemistry specifics, but it is heavy on a familiar operational theme: expanding menus and running them efficiently on existing platforms. That is exactly the kind of change that exposes whether the lab's middleware rules, QC processes, and data review steps are ready. Where this lands in lab budgets: interface work, validation time, and vendor accountability. For enterprise operators, the near-term spend is likely to tilt toward the connective tissue around automation. That includes LIS/LIMS interfaces, instrument drivers, audit trails, and the time to validate and train, especially when new AI capabilities are introduced into systems that already sit in the documentation path. The practical tell is whether a lab is writing requirements that treat the LIMS and the instrument as separate projects. ADLM's 2026 product messages, from Waters' performance framing to LabCollector's conversational ELN/LIMS features, suggest vendors are increasingly selling the workflow, even when they ship a box. Use this checklist to pressure-test whether vendors are selling a workflow, or shipping a box. * For new mass spec installs: what, exactly, is the comparator set behind "in-class" for sensitivity claims, and what acceptance tests will be run on your matrices and volumes, not a demo sample? (Waters' "5x" positioning was reported by SelectScience.) * For ELN/LIMS AI features: where does the model retrieve knowledge from inside your environment, what is the permission model, and how will generated content be flagged, reviewed, and version-controlled in the audit trail? (LabCollector's AI Co-Scientist capabilities were reported by SelectScience.) * For assay or menu expansions on existing analyzers: what middleware, QC, and reporting configuration changes are required, and who owns the validation workload and timeline? (Beckman Coulter's DxI 9000 infectious disease serology expansion was reported by SelectScience.) * For semi-automated workflows you plan to keep: which manual steps are staying manual because of true technical complexity, and which are manual because integration work has been deferred? (The semi-automated versus fully automated distinction is described by The Scientist.) Featured companies Your experts belong here Every story in MarketScale Sciences starts with a company putting its lab directors, applications scientists, and field specialists on the record. Buyers are already reading this topic. The only question is whose experts they find. Lab and research buyers verify before they trial, and your scientists give them something credible to verify against.

Associated Press
Aug 27th, 2026
LetsGetChecked launches FDA-cleared at-home HPV cervical cancer screening kit in the US

LetsGetChecked powered by Fuze Health has launched the Onclarity HPV Self-Collection Kit in the US, which it describes as the most comprehensive FDA-cleared at-home HPV cervical cancer screening tool currently available. The kit uses the BD Onclarity HPV Assay, which detects 14 high-risk HPV genotypes and identifies six individual genotypes. According to the National Cancer Institute, roughly one in four women in the US are not up to date with cervical cancer screening. The at-home testing aims to address barriers including logistical challenges, concerns about the screening experience, and limited awareness of options. LetsGetChecked previously received FDA De Novo authorisation in 2023 for an at-home chlamydia and gonorrhea sample collection system. The company has over 13 years of experience delivering at-home screening programmes.

BioPharma Watch
Aug 27th, 2026
Frequently asked questions.

Frequently asked questions. What is the new HPV screening tool from LetsGetChecked? It is the most comprehensive FDA-cleared at-home HPV screening tool available in the U.S. Who partnered with LetsGetChecked for this tool? LetsGetChecked partnered with Waters Corporation to develop the screening tool. What is the significance of this HPV screening tool? It enhances accessibility for patients to manage cervical cancer screening at home.

Business Wire
Aug 27th, 2026
LetsGetChecked launches most comprehensive FDA-cleared at-home HPV cervical cancer screening kit in US

LetsGetChecked powered by Fuze Health has launched the Onclarity HPV Self-Collection Kit, tested with the BD Onclarity HPV Assay, which it describes as the most comprehensive FDA-cleared at-home HPV screening tool available in the US. According to the National Cancer Institute, roughly one in four women in the US are not up to date with cervical cancer screening. The at-home kit aims to address barriers including concerns about the screening experience, logistical challenges, and limited awareness. The BD Onclarity HPV Assay detects 14 high-risk HPV genotypes and is the only FDA-approved HPV assay to identify six individual genotypes and three groups of pooled results. This builds on LetsGetChecked's 2023 FDA De Novo authorisation for an at-home chlamydia and gonorrhoea sample collection system.

Yahoo Finance
Aug 13th, 2026
Waters' Q2 revenue beats estimates at $1.65B as GLP-1 testing surges 40%

Waters Corporation reported second-quarter revenue of $1.65 billion, beating analyst estimates of $1.62 billion. The life sciences tools company posted adjusted earnings per share of $3.05, narrowly exceeding expectations of $3.01. CEO Udit Batra highlighted strong performance in GLP-1 testing, which grew over 40% during the quarter. The company credited robust demand across pharmaceutical, academic, and government markets, along with successful integration of recently acquired Biosciences and Diagnostic Solutions businesses. Management raised full-year adjusted EPS guidance to $14.55 at the midpoint. Third-quarter revenue guidance of $1.75 billion aligns with analyst expectations. During the earnings call, analysts questioned sustainability of growth in acquired businesses and pricing initiatives. Waters achieved 90 basis points of price realisation and is implementing deal desk processes to improve contract compliance and pricing discipline.