Global Change Facilitator – Regulatory CMC

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    "datePosted": "2026-05-28",
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    "description": "<p><span style=\"font-size: 12pt\">Global Change Facilitator – Regulatory CMC</span></p>\n<p><span style=\"font-size: 12pt\"><span style=\"font-weight: bold\">Location:</span> Home-based (UK) with international travel</span></p>\n<br>\n<p><span style=\"font-size: 12pt\">About BioPhorum</span></p>\n<p><span style=\"font-size: 12pt\">Established in 2004, BioPhorum is a leading business-to-business membership organisation that creates a unique environment for life sciences companies and executives to collaborate and accelerate progress across the sector.</span></p>\n<p><span style=\"font-size: 12pt\">With a subscription-based model, BioPhorum delivers 12 highly focused “Phorums” covering key areas including Drug Substance, Drug Development, Fill Finish, Technology Strategy, Supply Chain Resilience, Data &amp; Digital, ATMPs, Quality, Regulatory, and Sustainability.</span></p>\n<p><span style=\"font-size: 12pt\">Today, more than 7,000 subject matter experts from over 150 organisations — including 18 of the world’s top 20 biopharma companies — collaborate through BioPhorum’s facilitated workstreams to solve industry-wide challenges and shape future best practices.</span></p>\n<p><span style=\"font-size: 12pt\">Following a period of strong growth, including new product launches and acquisitions, BioPhorum is entering an exciting new phase of expansion — and we are looking for a Global Change Facilitator to join our Regulatory CMC Phorum.</span></p>\n<br>\n<p><span style=\"font-size: 12pt\">The Role</span></p>\n<p><span style=\"font-size: 12pt\">As a Global Change Facilitator within the Regulatory CMC Phorum, you will play a key role in enabling collaboration across the global biopharmaceutical industry. You will facilitate expert-led workstreams focused on Chemistry, Manufacturing and Controls (CMC) regulatory challenges, helping members share insights, align on best practices, and drive meaningful industry outcomes.</span></p>\n<p><span style=\"font-size: 12pt\">Blending facilitation, project leadership, scientific understanding, and stakeholder engagement, you will create high-performing collaborative environments where complex regulatory and operational topics are translated into practical, impactful deliverables.</span></p>\n<p><span style=\"font-size: 12pt\">This is a highly collaborative and fast-paced role requiring strong communication skills, organisational capability, adaptability, and a proactive approach.</span></p>\n<br>\n<p><span style=\"font-size: 12pt\">Key Responsibilities</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Facilitate and lead a portfolio of Regulatory CMC workstreams, ensuring delivery of high-quality industry outputs and measurable member value</span></li>\n<li><span style=\"font-size: 12pt\">Create engaging and collaborative environments that encourage participation, knowledge-sharing, and industry alignment</span></li>\n<li><span style=\"font-size: 12pt\">Guide workstreams using structured project and change management approaches to deliver agreed objectives on time</span></li>\n<li><span style=\"font-size: 12pt\">Design and facilitate both virtual and in-person meetings, workshops, and events for senior industry stakeholders</span></li>\n<li><span style=\"font-size: 12pt\">Co-develop impactful deliverables including industry guidance, position papers, best practice frameworks, proof-of-concepts, and conference content</span></li>\n<li><span style=\"font-size: 12pt\">Monitor member engagement and proactively identify and resolve risks or barriers to progress</span></li>\n<li><span style=\"font-size: 12pt\">Maintain and optimise internal systems, reporting tools, and collaboration platforms</span></li>\n<li><span style=\"font-size: 12pt\">Capture and communicate value stories demonstrating the impact of industry collaboration</span></li>\n<li><span style=\"font-size: 12pt\">Feed member insights back into the organisation to support continuous improvement and future Phorum development</span></li>\n</ul>\n<br>\n<p><span style=\"font-size: 12pt\">About the Regulatory CMC Phorum</span></p>\n<p><span style=\"font-size: 12pt\">The regulatory landscape for CMC continues to evolve rapidly, driven by increasing product complexity, accelerated development timelines, global regulatory divergence, digitalisation, and emerging manufacturing technologies.</span></p>\n<p><span style=\"font-size: 12pt\">In this role, you will help drive industry-wide collaboration and innovation by supporting initiatives focused on:</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Regulatory harmonisation and convergence</span></li>\n<li><span style=\"font-size: 12pt\">CMC lifecycle management and post-approval change management</span></li>\n<li><span style=\"font-size: 12pt\">Digital and data-enabled regulatory approaches</span></li>\n<li><span style=\"font-size: 12pt\">Global submission and regulatory strategy challenges</span></li>\n<li><span style=\"font-size: 12pt\">Emerging modalities and advanced manufacturing approaches</span></li>\n<li><span style=\"font-size: 12pt\">Inspection readiness and evolving regulatory expectations</span></li>\n<li><span style=\"font-size: 12pt\">Industry best practices for CMC development and compliance</span></li>\n</ul>\n<p><span style=\"font-size: 12pt\">You will work alongside senior leaders and subject matter experts from across the global biopharma ecosystem to help shape the future of Regulatory CMC.</span></p>\n<br>\n<p><span style=\"font-size: 12pt\">About You</span></p>\n<p><span style=\"font-size: 12pt\">You are a collaborative, intellectually curious professional who enjoys working in complex environments and bringing people together to solve meaningful industry challenges.</span></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt\">Essential Experience &amp; Skills</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Degree-level education or equivalent experience within life sciences, pharmaceuticals, biotechnology, regulatory affairs, or related disciplines</span></li>\n<li><span style=\"font-size: 12pt\">Strong understanding of Regulatory CMC within the biopharmaceutical industry</span></li>\n<li><span style=\"font-size: 12pt\">Experience working within pharmaceutical, biotechnology, CDMO, consulting, or regulatory environments</span></li>\n<li><span style=\"font-size: 12pt\">Proven experience managing projects, initiatives, or change programmes</span></li>\n<li><span style=\"font-size: 12pt\">Strong facilitation and stakeholder management capability</span></li>\n<li><span style=\"font-size: 12pt\">Ability to synthesise complex technical and regulatory information into clear, actionable insights</span></li>\n<li><span style=\"font-size: 12pt\">Excellent organisational skills with the ability to manage multiple priorities and deliver against timelines</span></li>\n<li><span style=\"font-size: 12pt\">Comfortable operating within fast-paced, evolving environments</span></li>\n<li><span style=\"font-size: 12pt\">Confident working remotely and collaborating across global teams and cultures</span></li>\n</ul>\n<br>\n<p><span style=\"font-size: 12pt\">You Will Also Be</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">A natural facilitator who enjoys enabling collaboration and productive discussion</span></li>\n<li><span style=\"font-size: 12pt\">A strong communicator who can influence and engage diverse stakeholder groups</span></li>\n<li><span style=\"font-size: 12pt\">A proactive and solutions-focused problem solver</span></li>\n<li><span style=\"font-size: 12pt\">A collaborative team player who values continuous improvement and feedback</span></li>\n<li><span style=\"font-size: 12pt\">Curious, adaptable, and motivated by industry impact</span></li>\n</ul>\n<br>\n<p><span style=\"font-size: 12pt\">Why Join BioPhorum?</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Work at the forefront of global life sciences collaboration</span></li>\n<li><span style=\"font-size: 12pt\">Influence industry-wide regulatory and operational change</span></li>\n<li><span style=\"font-size: 12pt\">Collaborate with leading experts from across the global biopharma sector</span></li>\n<li><span style=\"font-size: 12pt\">Join a growing, forward-thinking organisation</span></li>\n<li><span style=\"font-size: 12pt\">Enjoy a flexible, remote-first working environment with international exposure</span></li>\n</ul>\n<br>\n<p><span style=\"font-size: 12pt\">Apply Now</span></p>\n<p><span style=\"font-size: 12pt\">If you are passionate about driving collaboration and innovation within the life sciences industry and thrive in a high-impact, fast-paced environment, we would love to hear from you.</span></p>",
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