
Business Development Manager β Facility Validation, Environmental Monitoring, Calibration
Posted Sep 10

Posted Sep 10
This is a fully remote position, open to applicants in Netherlands.
β’ Meet or surpass yearly revenue goals for facility validation, environmental monitoring, and calibration/metrology services.
β’ Utilize established relationships to deepen account penetration and seek out new clients.
β’ Create and execute focused sales strategies for facility validation and instrument qualification/calibration services.
β’ Employ industry websites, construction databases, trade publications, associations, regulatory filings, and market research to discover new construction opportunities.
β’ Conduct in-person client meetings, lead discussions with stakeholders, and finalize contracts.
β’ Aim for 15 in-person client meetings each month with key decision-makers.
β’ Manage the opportunity pipeline using CRM tools.
β’ Follow up on pending proposals and document closure details for opportunities.
β’ Provide monthly reports on wins, losses, and open opportunities to sales and operational leadership.
β’ Act as a subject matter expert in facility validation, environmental monitoring, and calibration/metrology.
β’ Collaborate with Business Unit leaders to align programs with laboratory capabilities throughout the Eurofins network.
β’ Comprehend client scientific, regulatory, and business needs to develop technical work scopes and solutions.
β’ Organize project hand-off meetings with project management and operations teams.
β’ Keep abreast of industry trends, competitor actions, and regulatory developments.
β’ Participate in industry conferences and trade shows to network and promote services.
β’ Located in the Western US.
β’ Bachelor's or advanced degree in life sciences, environmental sciences, engineering, or business administration.
β’ At least 3 years of applicable sales experience in facility validation/environmental monitoring and/or instrument calibration/metrology services.
β’ Familiarity with biopharmaceutical and/or medical device manufacturing.
β’ Demonstrated history of achieving or surpassing sales targets.
β’ Willingness to travel at least 40% of the time.
β’ Must have authorization to work in the United States indefinitely without restrictions or sponsorship.
β’ Knowledge of regulatory requirements and industry standards, including FDA, cGMP, and ISO 17025.
β’ Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.
β’ Life and disability insurance.
β’ 401(k) plan with company match.
β’ Paid vacation and holidays.
β’ Full-time schedule from Monday to Friday, 8 a.m. to 5 p.m., with overtime as necessary.
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