Global Change Facilitator – Regulatory CMC

Global Change Facilitator – Regulatory CMCLocation: Home-based (UK) with international travelAbout BioPhorumEstablished 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.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 & Digital, ATMPs, Quality, Regulatory, and Sustainability.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.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.The RoleAs 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.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.This is a highly collaborative and fast-paced role requiring strong communication skills, organisational capability, adaptability, and a proactive approach.Key ResponsibilitiesFacilitate and lead a portfolio of Regulatory CMC workstreams, ensuring delivery of high-quality industry outputs and measurable member valueCreate engaging and collaborative environments that encourage participation, knowledge-sharing, and industry alignmentGuide workstreams using structured project and change management approaches to deliver agreed objectives on timeDesign and facilitate both virtual and in-person meetings, workshops, and events for senior industry stakeholdersCo-develop impactful deliverables including industry guidance, position papers, best practice frameworks, proof-of-concepts, and conference contentMonitor member engagement and proactively identify and resolve risks or barriers to progressMaintain and optimise internal systems, reporting tools, and collaboration platformsCapture and communicate value stories demonstrating the impact of industry collaborationFeed member insights back into the organisation to support continuous improvement and future Phorum developmentAbout the Regulatory CMC PhorumThe regulatory landscape for CMC continues to evolve rapidly, driven by increasing product complexity, accelerated development timelines, global regulatory divergence, digitalisation, and emerging manufacturing technologies.In this role, you will help drive industry-wide collaboration and innovation by supporting initiatives focused on:Regulatory harmonisation and convergenceCMC lifecycle management and post-approval change managementDigital and data-enabled regulatory approachesGlobal submission and regulatory strategy challengesEmerging modalities and advanced manufacturing approachesInspection readiness and evolving regulatory expectationsIndustry best practices for CMC development and complianceYou will work alongside senior leaders and subject matter experts from across the global biopharma ecosystem to help shape the future of Regulatory CMC.About YouYou are a collaborative, intellectually curious professional who enjoys working in complex environments and bringing people together to solve meaningful industry challenges.Essential Experience & SkillsDegree-level education or equivalent experience within life sciences, pharmaceuticals, biotechnology, regulatory affairs, or related disciplinesStrong understanding of Regulatory CMC within the biopharmaceutical industryExperience working within pharmaceutical, biotechnology, CDMO, consulting, or regulatory environmentsProven experience managing projects, initiatives, or change programmesStrong facilitation and stakeholder management capabilityAbility to synthesise complex technical and regulatory information into clear, actionable insightsExcellent organisational skills with the ability to manage multiple priorities and deliver against timelinesComfortable operating within fast-paced, evolving environmentsConfident working remotely and collaborating across global teams and culturesYou Will Also BeA natural facilitator who enjoys enabling collaboration and productive discussionA strong communicator who can influence and engage diverse stakeholder groupsA proactive and solutions-focused problem solverA collaborative team player who values continuous improvement and feedbackCurious, adaptable, and motivated by industry impactWhy Join BioPhorum?Work at the forefront of global life sciences collaborationInfluence industry-wide regulatory and operational changeCollaborate with leading experts from across the global biopharma sectorJoin a growing, forward-thinking organisationEnjoy a flexible, remote-first working environment with international exposureApply NowIf 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.DepartmentRegulatory CMCEmployment TypeFull Time EmployeeMinimum ExperienceExperienced