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2 дня назад

Senior Specialist, Technical Evaluations & Proposals (Biopharma)

80 000 - 117 500$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
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
Senior Specialist, Technical Evaluations & Proposals (Biopharma): Developing technical and commercial proposals for biologics, drug product manufacturing, R&D, technology platforms, and process and analytical development with an accent on customer requirement analysis, technical fit assessments, costing, and pricing. Focus on coordinating subject matter experts, managing proposal pipelines, incorporating contractual terms, and progressing scopes from proposal to contract signature.

Location: Remote within the United States; listed location: Ohio, USA. Travel up to 10% and non-standard working hours may be required.

Salary: $80,000–$117,500 per year, depending on location, experience, qualifications, skills, and knowledge.

Company

hirify.global is a technology-focused biomanufacturing company developing sustainable, end-to-end manufacturing solutions for medicines and scientific discovery.

What you will do

  • Evaluate customer RFIs and RFPs, clarify technical needs, and develop proposal strategies.
  • Generate proposals for biologics, sterile drug products, advanced R&D, technology platforms, process and analytical development, and GMP manufacturing.
  • Collaborate with subject matter experts across global sites to assess technical fit and revise project scopes.
  • Work with Sales, Business Management, and Commercial Development to establish profitable pricing and timelines.
  • Manage the proposal pipeline, customer expectations, and the process from proposal development through contract signature.
  • Support costing, pricing analysis, assigned technical evaluation projects, and continuous improvement initiatives.

Requirements

  • Fundamental understanding of biologics and/or sterile drug product manufacturing and the drug development lifecycle.
  • Strong attention to detail, analytical ability, organization, time management, and communication skills.
  • Ability to work effectively in a matrix environment, prioritize proactively, and manage multiple tasks.
  • Proficiency with MS Word and/or MS Project, Excel, and PowerPoint.
  • Must be authorized to work in the United States; visa and work authorization sponsorship is not available.
  • Ability to work remotely within the United States, travel up to 10%, and work flexible non-standard hours.

Nice to have

  • 2–4 years of bio/pharmaceutical R&D or manufacturing experience, preferably in a CDMO.
  • 0–3 years of technical evaluation and proposal experience.
  • Salesforce CRM experience or prior customer-facing experience.
  • Program management, sales, business, or technical experience.
  • Experience writing drug product proposals.

Culture & Benefits

  • Annual cash bonus program and 401(k) plan with company match.
  • Medical, dental, and vision healthcare benefits.
  • Family-building benefits, life and disability insurance, and caregiving support.
  • Paid vacation, paid holidays, and other paid leave.
  • Tuition reimbursement and professional development support.

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