Manager, Drug substance, Commercial Manufacturing Operations
BridgeBio Pharma(1 month ago)
About this role
The role is responsible for managing relationships with API contract manufacturers and regulatory starting material suppliers to support BridgeBio programs, acting as a technical and operational lead across CMC functions. The position interfaces with QA/RA and supply chain, supports regulatory filings and translation to production activities, and promotes continuous improvement and high-performance teamwork. The role is based in the Netherlands and involves regular collaboration with internal teams and up to ~20% travel for plant support and tech transfers.
Required Skills
- CMO Management
- Supplier Management
- Technical Transfer
- Process Validation
- Documentation Review
- Batch Disposition
- Investigation Oversight
- CAPA Management
- Process Improvement
- Regulatory Knowledge
+4 more
Qualifications
- PhD in Organic Chemistry
- MS in Chemistry
- BS in Chemistry
About BridgeBio Pharma
bridgebio.comBridgeBio is a biotechnology company designing transformative medicines for patients with genetic diseases and cancers driven by clear genetic causes. The company advances programs from target discovery through clinical development, combining human genetics and translational science with rigorous clinical trials to create targeted therapeutics. BridgeBio builds a diversified portfolio of wholly owned and partnered programs across multiple modalities and uses a venture‑style operating model to accelerate and de‑risk development. Its mission is to translate genetic insights into precision medicines for patients with high unmet medical need.
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