At a Glance
- Tasks: Facilitate collaboration on regulatory challenges in the biopharmaceutical industry.
- Company: Join BioPhorum, a leader in life sciences collaboration.
- Benefits: Flexible remote work, international exposure, and a chance to influence industry change.
- Other info: Dynamic role with opportunities for professional growth and development.
- Why this job: Make a real impact by driving innovation and collaboration in life sciences.
- Qualifications: Degree in life sciences or related field; experience in regulatory CMC preferred.
The predicted salary is between 60000 - 80000 £ per year.
Location: Home-based (UK) with international travel
About BioPhorum
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. 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 Role
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. 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 Responsibilities
- Facilitate and lead a portfolio of Regulatory CMC workstreams, ensuring delivery of high-quality industry outputs and measurable member value
- 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
About the Regulatory CMC Phorum
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. In this role, you will help drive industry-wide collaboration and innovation by supporting initiatives focused on:
- Regulatory harmonisation and convergence
- CMC lifecycle management and post-approval change management
- Digital and data-enabled regulatory approaches
- Global submission and regulatory strategy challenges
- Emerging modalities and advanced manufacturing approaches
- Inspection readiness and evolving regulatory expectations
- Industry best practices for CMC development and compliance
You will work alongside senior leaders and subject matter experts from across the global biopharma ecosystem to help shape the future of Regulatory CMC.
About You
You are a collaborative, intellectually curious professional who enjoys working in complex environments and bringing people together to solve meaningful industry challenges.
Essential Experience & Skills
- 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
You Will Also Be
- A natural facilitator who enjoys enabling collaboration and productive discussion
- A strong communicator who can influence and engage diverse stakeholder groups
- A proactive and solutions-focused problem solver
- A collaborative team player who values continuous improvement and feedback
- Curious, adaptable, and motivated by industry impact
Why Join BioPhorum?
- Work at the forefront of global life sciences collaboration
- Influence industry-wide regulatory and operational change
- Collaborate with leading experts from across the global biopharma sector
- Join a growing, forward-thinking organisation
- Enjoy a flexible, remote-first working environment with international exposure
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.
Global Change Facilitator – Regulatory CMC in London employer: BioPhorum
BioPhorum is an exceptional employer that fosters a collaborative and innovative work culture, allowing employees to engage with leading experts in the biopharmaceutical sector. With a flexible, remote-first environment and opportunities for international travel, team members can influence industry-wide regulatory changes while enjoying professional growth and development. Joining BioPhorum means being part of a forward-thinking organisation dedicated to making a meaningful impact in life sciences.
StudySmarter Expert Advice🤫
We think this is how you could land Global Change Facilitator – Regulatory CMC in London
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend relevant events. Building connections can open doors and give you insider info about job opportunities.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with your own. This will help you stand out as a candidate who truly fits in.
✨Tip Number 3
Practice your communication skills. As a Global Change Facilitator, you'll need to convey complex ideas clearly. Mock interviews with friends can help you refine your pitch and boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Global Change Facilitator – Regulatory CMC in London
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in Regulatory CMC and project management. We want to see how your skills align with the role, so don’t hold back on showcasing your relevant achievements!
Showcase Your Collaboration Skills:Since this role is all about facilitating collaboration, share examples of how you've successfully worked with diverse teams or stakeholders in the past. We love to see how you bring people together to solve challenges!
Be Clear and Concise:When writing your application, keep it straightforward and to the point. Use clear language to convey your ideas and experiences, as we appreciate candidates who can communicate effectively—just like the role requires!
Apply Through Our Website:We encourage you to submit your application through our website for a smoother process. It’s the best way for us to receive your details and get you into our system quickly. Plus, it shows you’re keen to join our team!
How to prepare for a job interview at BioPhorum
✨Know Your CMC Inside Out
Make sure you brush up on your knowledge of Chemistry, Manufacturing, and Controls (CMC) regulations. Familiarise yourself with the latest trends and challenges in the biopharmaceutical industry, as this will help you engage in meaningful discussions during the interview.
✨Showcase Your Facilitation Skills
Prepare to demonstrate your facilitation abilities by discussing past experiences where you've led collaborative projects or workshops. Be ready to share specific examples of how you created engaging environments that encouraged participation and knowledge-sharing among diverse stakeholders.
✨Be Proactive and Solutions-Focused
During the interview, highlight your proactive approach to problem-solving. Share instances where you've identified risks or barriers in previous roles and how you successfully navigated them. This will show your potential employer that you're not just a thinker but also a doer.
✨Communicate Clearly and Confidently
Strong communication skills are essential for this role. Practice articulating complex regulatory information in a clear and concise manner. You might even want to prepare a few key points about how you would communicate value stories to stakeholders, as this is crucial for demonstrating impact.
