Added: 2025-05-28 14:15.00
Updated: 2025-05-30 03:30.34

Global Business Development Manager, Products

Leiden , South Holland, Netherlands

Type: n/a

Category: Sales

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Requirements: English
Company: Ncardia
Region: Leiden , South Holland

The position can also be based in the US.

About the Position

The Global Business Development Manager for iPSC Products will be a highly motivated individual with proven sales experience within the Life Sciences industry. They are responsible for the direct selling activities of Ncardias catalog products and will lead strategic and tactical efforts to expand the customer base, drive revenue growth, and increase market share for our portfolio of iPSC-derived products. They will develop a consultative selling approach offering a strong value proposition to the customer experience. This Global Business Development Manager will win opportunities by providing customers with intellectual input into project design drawing on their own scientific acumen and pulling in other technical specialists when required. The market will recognize this individual as offering best in class scientific/product knowledge, and an unmatched understanding of customer needs.

Responsibilities and Duties

Qualifications and Skills

Preferred Attributes

Role Deliverables

Application Process

Interested candidates should submit their resume and cover letter to careers@ncardia.com.

Company Overview

At Ncardia, we believe that stem technology will help get better therapies to patients faster. The goal of the company is to be the supportive and trusted partner for scientists operating within the induced pluripotent stem cell (iPSC) drug discovery and cell therapy fields, and in particular, in the cardiovascular and neurology space. Ncardia develops, produces, and commercializes highly predictive cardiovascular and neurological cellular assay systems. In addition, Ncardia develops and provides its customers with a broad portfolio of services from cardiovascular and neuronal disease modelling to target discovery and validation, primary or secondary drug screening, hit to lead and lead optimization, safety assessment, and pre-clinical patient stratification.

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