Global Change Facilitator – Regulatory CMC

🕒 May 29

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BioPhorum

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2008

🧬 Biotechnology

💊 Pharmaceuticals

💰 Private Equity Round on 2008-05

Biotechnology • Pharmaceuticals

BioPhorum is a collaborative organization that enables the global biopharmaceutical industry to connect, collaborate, and accelerate progress for the benefit of all. It brings together therapy developers, contract manufacturing and testing organizations to address challenges and share solutions in the biopharmaceutical industry, particularly in areas such as advanced therapy medicinal products, drug delivery, drug substance manufacturing, fill finish operations, and digital transformation. BioPhorum acts as an industry voice to facilitate regulatory convergence, enhance supply chain resilience, and support sustainability efforts through multi-disciplinary collaboration and innovative technology strategies.

📋 Description

• Facilitate and lead a portfolio of Regulatory CMC workstreams • Create engaging and collaborative environments that encourage participation, knowledge-sharing, and industry alignment • Guide workstreams using structured project and change management approaches to deliver agreed objectives on time • Design and facilitate both virtual and in-person meetings, workshops, and events for senior industry stakeholders • Co-develop impactful deliverables including industry guidance, position papers, best practice frameworks, proof-of-concepts, and conference content • Monitor member engagement and proactively identify and resolve risks or barriers to progress • Maintain and optimise internal systems, reporting tools, and collaboration platforms • Capture and communicate value stories demonstrating the impact of industry collaboration • Feed member insights back into the organisation to support continuous improvement and future Phorum development

🎯 Requirements

• Degree-level education or equivalent experience within life sciences, pharmaceuticals, biotechnology, regulatory affairs, or related disciplines • Strong understanding of Regulatory CMC within the biopharmaceutical industry • Experience working within pharmaceutical, biotechnology, CDMO, consulting, or regulatory environments • Proven experience managing projects, initiatives, or change programmes • Strong facilitation and stakeholder management capability • Ability to synthesise complex technical and regulatory information into clear, actionable insights • Excellent organisational skills with the ability to manage multiple priorities and deliver against timelines • Comfortable operating within fast-paced, evolving environments • Confident working remotely and collaborating across global teams and cultures

🏖️ Benefits

• Flexible working environment • International exposure