Senior Associate – CMC Consulting (Pharma/Biotech)
pwc · Brussels
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.
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Published 1 maand geleden
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pwc
Brussels
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