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Business Development Manager non-sterile drug product development and manufacturing - Eurofins CDMO at Resillion Netherlands

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in a scientific field, 5-10 years of experience selling services from formulation development to packaging including analytical support., Strong understanding of drug product development and manufacturing for small and large molecules. Excellent communication skills and willingness to travel..

Key responsabilities:

  • Prospect clients in Europe and focus on development projects up to clinical phases 1-2B.
  • Represent CDMO division at conferences and analyze competitors. Collaborate with other sites closely.
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Resillion Netherlands SME https://www.eurofins-cybersecurity.com/
51 - 200 Employees
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Job description

Company Description

Eurofins CDMO is a leading international Contract Development and Manufacturing Organization (CDMO) based in Europe. Our company focuses on drug product development and manufacturing for chemical/biological entities and drug substance development and manufacturing for biological entities. We support small and major biopharmaceutical companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our facilities are perfectly designed for clinical and/or small scale commercial batches either for non-sterile or sterile dosage forms. With approximatively 350 staff, we operate out of 8 sites in France, Belgium and Italy.

Job Description

To support our ambitious growth plan in formulation, analytical development and manufacturing of clinical batches and small scale commercial batches, we are today looking for a talented Business Development Manager Non-Sterile Drug Product Development and Manufacturing.

Reporting to the Head Business Development, you will work closely with our Technical Business Managers (compiling quotations) and our different Business Unit Managers (managing sites) to achieve your assigned objectives. The ideal candidate will be in charge of:

  • Enlarging client portfolio through active prospection in Europe
  • Focusing on development projects particularly the earliest phases up to clinical development (Phase 1 to 2B) for chemical and/or biological compounds
  • Representing the CDMO division on relevant conferences, workshops and tradeshows
  • Benchmarking our offering versus identified competitors or newcomers

This position will primarily focus on our site in Ghent but can also serve our facilities located in Bordeaux (FR), Montpellier (FR) or Idron (FR) with whom the candidate will closely collaborate.

Qualifications

Graduated with a scientific degree (Engineer, Msc, PhD), we would expect at least 5 to 10 years of relevant experience in selling full package services from formulation development, drug product development to packaging including analytical support and manufacturing for small or large molecules.

Good communicator, dynamic, strong business acumen with an understanding of the drug product development and manufacturing requirements for small molecules and biologics. You are willing to travel intensively (50% of your time). Even if autonomous, you like to feel part of a team. Absolutely fluent in English, another language such as French, Dutch/Flemish or German would be a plus.

This position would be ideally located in Ghent or surroundings. Nevertheless, we are open for good candidates in other locations with good flight connections.

Additional Information
  • Work in a fast growing organization.
  • A position with responsibility within a dynamic company.
  • Personal development through learning on the job and additional external trainings.
  • A market oriented compensation.

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
Check out the description to know which languages are mandatory.

Other Skills

  • Business Acumen
  • Sales
  • Teamwork
  • Communication

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