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Bioprocess Subject Matter Expert (SME)

Формат работы
hybrid
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
Bioprocess Subject Matter Expert (SME) (Biologics/Advanced Therapeutics): Providing technical leadership for pharmaceutical, biologics, and cell and gene therapy manufacturing projects from feasibility and conceptual design through qualification and operational readiness with an accent on process development, facility design, and client-facing technical leadership. Focus on developing bioprocess deliverables, supporting proposals and business development, facilitating technical reviews and workshops, and solving complex design problems for US and international clients.

Location: Hybrid in Conshohocken, Pennsylvania, supporting the Philadelphia area and projects across the United States; periodic travel to client sites is required.

Company

hirify.global is an employee-owned international project delivery firm serving pharmaceutical, food, biotech, medical technology, and mission-critical sectors through offices in Europe, Asia, and the United States.

What you will do

  • Provide technical leadership for biologics and advanced therapeutics projects.
  • Support business development through prospecting, client visits, pitches, proposal writing, presentations, and bid reviews.
  • Act as a bioprocess SME during site master planning, feasibility, concept, and basic design phases.
  • Develop and review process deliverables, including throughput analyses, flow diagrams, equipment requirements, mass balances, simulation models, P&IDs, adjacency diagrams, and layout philosophies.
  • Facilitate client workshops, technical design reviews, peer reviews, and client-site SME assessments.
  • Build internal capabilities by mentoring subject matter experts, sharing knowledge, and contributing to technology and innovation initiatives.

Requirements

  • 15+ years of relevant experience in design, operations, or process development.
  • Superior knowledge of biologics and advanced therapies, facility layout and design, and applicable regulatory frameworks.
  • Industry engagement with organizations such as ISPE and awareness of key technology initiatives.
  • Strong presentation, problem-solving, innovation, relationship-building, and client-interfacing skills.
  • Ability to work independently and collaboratively with multinational clients and teams.
  • Ability to work flexibly and travel as required for business and client needs.

Culture & Benefits

  • Employee-owned organization focused on people, clients, and trade partners.
  • Inclusive workplace committed to mutual respect, belonging, and diversity.
  • Opportunities to work on international pharmaceutical, biotech, and advanced therapeutics projects.
  • Commitment to corporate responsibility and sustainability.
  • Reasonable accommodations are available during the recruitment process.

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