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1 месяц назад

Business Development Director (Biopharma)

Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Business Development Director (Biopharma): Developing and closing biopharmaceutical customer and partnership opportunities with an accent on technical business development, client relationships, proposals, and contract negotiations. Focus on coordinating complex life science projects, advancing long-cycle sales processes, and building partnerships across scientific, legal, quality, and management stakeholders.

Location: Plan-les-Ouates, Switzerland

Company

hirify.global provides biopharmaceutical process development and manufacturing services.

What you will do

  • Identify potential biopharmaceutical clients, qualify leads, build relationships, solicit RFPs, and manage proposals through contract closure.
  • Expand business with existing accounts and support key client relationships alongside the Vice President of Business Development.
  • Develop and advance scientific partnerships, collaborations, licensing opportunities, joint ventures, and alliances.
  • Present KBI capabilities at client sites, trade shows, and scientific meetings, and coordinate client technical visits to KBI sites.
  • Coordinate CDA and MSA reviews, quality audits, quality agreements, and contract negotiations with legal, quality, scientific, and client stakeholders.
  • Maintain CRM opportunity data and industry awareness while leading internal stakeholders toward business development objectives.

Requirements

  • Technical PhD or MSc degree, preferably in science, with at least 4 years of business development experience in the life sciences industry.
  • Proven success in technical business development, preferably in contract services or capital equipment.
  • Experience with prospecting, client presentations, RFPs, proposals, objection handling, and closing contracts.
  • Experience working with corporate partners and negotiating and completing agreements.
  • Familiarity with biopharmaceutical manufacturing and regulatory requirements, or the ability to learn them quickly.
  • Ability to travel up to 50% for client visits, KBI site meetings, trade shows, and scientific meetings.

Culture & Benefits

  • Full-time employment.
  • Work involves collaboration with scientific, technical, legal, quality, marketing, and management stakeholders.
  • Team-based environment focused on building positive internal and external working relationships.
  • Equal opportunity employer committed to workforce diversity.

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