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Senior Associate – CMC Consulting (Pharma/Biotech)

pwc · Brussels

Senior 🇬🇧 English
Regulatory compliance Digitalization Manufacturing scale-up Process validation

Job description

About the role

PwC is expanding its footprint in the health industry and seeks a Senior Associate to lead CMC (Chemistry, Manufacturing, and Controls) projects for pharmaceutical and biotechnology clients. You will work within a multidisciplinary advisory team to help clients navigate regulatory, operational, and technological challenges.

Key responsibilities

  • Manage CMC projects, including strategic assessment, recommendation development, and implementation of new operating models.
  • Act as PM/PMO for CMC departments, overseeing timelines, budgets, and risk management.
  • Provide subject‑matter expertise on CMC‑focused initiatives such as supply‑chain optimization, digitalization, regulatory compliance, manufacturing scale‑up, process validation, and technology transfer.
  • Contribute to PwC’s CMC centre of excellence and support business development activities.
  • Produce thought‑leadership content, market analyses, and point‑of‑view papers.

Required profile

  • Master’s degree in biomedical sciences, economics, bio‑engineering, business administration, or a related field.
  • Passion for CMC processes and regulatory compliance.
  • 2–5 years of experience in the life‑science industry or consultancy with a focus on CMC projects.
  • Knowledge of advanced‑therapy challenges, market trends, and key industry players.
  • Strong analytical and problem‑solving abilities combined with specialist technical knowledge.

Required skills

  • Project management (PM/PMO) for CMC initiatives.
  • Regulatory compliance expertise.
  • Supply‑chain optimization.
  • Digitalization of CMC processes.
  • Manufacturing scale‑up.
  • Process validation.
  • Technology transfer.

Questions fréquentes

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Source : ats:workday

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Published 1 maand geleden

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Brussels