Senior QA Officer

Senior Supply Chain Manager

We are exclusively partnered with an ambitious CDMO undergoing transformation across its operations and supply chain functions. As investment continues and the business scales, a key leadership opportunity has emerged for an experienced Senior Supply Chain Manager to play a pivotal role in driving operational excellence and cultural change.
This is far more than a functional leadership role. You'll be at the centre of a business-wide transformation, helping to modernise planning processes, introduce new ways of working, and build a highly engaged team capable of supporting future growth.
What you'll be doing
This role has three key areas of focus:
• Leading the development and implementation of a new scheduling and planning tool.
• Driving engagement, adoption and cultural change across the planning function.
• Taking ownership of both Warehouse Logistics and Production Planning operations, ensuring the smooth execution of day-to-day activities while building for the future.
Success in this position will require someone who is equally comfortable operating strategically and spending time on the shop floor understanding the realities of the operation. You'll lead from the front, bringing teams with you through change while maintaining a relentless focus on service, efficiency and continuous improvement.
What we're looking for
• Supply chain leadership experience within pharmaceuticals, food manufacturing or FMCG.
• Strong background in production planning and scheduling.
• Proven experience leading transformation or change initiatives.
• Demonstrated success managing and developing teams.
• Ability to drive engagement, influence stakeholders and create buy-in across functions.
• A hands-on leadership style with a genuine understanding of operational environments.
• GMP experience would be advantageous but is not essential.
Why consider this opportunity?
• Play a key role in a business undergoing significant growth and investment.
• Lead a high-profile transformation programme with visible impact.
• Shape the future direction of critical supply chain functions.
• Join a company where your leadership and ideas will directly influence success.
• Be part of a collaborative, ambitious leadership team committed to building a best-in-class operation.

For further details, please contact Mark Bux-Ryan
Supply, chain, cdmo, pharmaceutical, food, manufacturing, FMCG, planning, production, warehouse, logistics, leadership, manager, head, change, transformation, GMP

If you’re a newly promoted or established Senior Account Manager who’s ready for the opportunity to really show what you can do, this could be a very good next move.

We’re partnering with a growing independent healthcare communications agency where you’ll have the freedom to take ownership, bring ideas to the table and have a voice across the agency.

The role

You’ll take a leading role across significant healthcare accounts, with a particular focus on neurology and women’s health, spanning product and above-brand communications.

You’ll be trusted to:

• Lead day-to-day client relationships and provide communications counsel

• Own and drive projects and workstreams

• Support major product and regulatory milestones

• Lead European disease awareness, education and KOL engagement programmes

• Bring ideas and solutions rather than simply take briefs

• Spot opportunities to strengthen and grow client accounts

• Mentor and develop junior colleagues

What you'll bring

Must-haves:

• SAM-level healthcare PR/communications agency experience

• Product and above-brand communications experience

• Experience supporting significant product or regulatory milestones

• Strong client leadership and stakeholder management skills

Ideally, you’ll also have European or multi-market experience and/or a scientific background.

This could be you

You’re confident, proactive and comfortable taking the lead. You use your judgement, bring recommendations to clients and want the freedom to make an impact rather than simply deliver what lands on your desk.

You’re commercially aware, enjoy developing others and want to be somewhere your contribution is visible and your voice is heard.

Why this opportunity?

Whether you’ve recently stepped up to SAM or you’re established at this level and looking for more scope, you’ll have ownership of important client work, visibility with senior leadership and the freedom to shape your role as the agency grows.

For a confidential chat about this role or your next career move, please contact Nicky Stunt, Principal Healthcare Communications Consultant, at nicky.stunt@rbwconsulting.com.

Senior Regulatory Consultant – Small Molecule Registration (Lead)

Late-Stage Small Molecule | Global Regulatory Strategy | MAA Preparation

A rare opportunity has arisen for an experienced Regulatory CMC leader to take ownership of a high-profile late-stage small molecule programme approaching Marketing Authorisation submission.

This role sits at the heart of a global development team and offers the chance to shape CMC regulatory strategy for a key asset at one of the most exciting stages of the product lifecycle.

You'll be the driving force behind the global CMC regulatory roadmap, partnering with technical development, manufacturing, quality, supply chain and regulatory stakeholders to ensure successful delivery of a complex registration programme.

The Opportunity

This is more than a traditional Regulatory Affairs role.

You'll act as the strategic CMC lead for a late-stage development asset, defining and executing global regulatory strategy, preparing for key Health Authority interactions, identifying risks early, and ensuring a high-quality CMC dossier is delivered on time.

Working within a highly collaborative international environment, you'll influence critical development decisions, support accelerated development pathways and play a key role in bringing an important new medicine to patients worldwide.

What You'll Be Doing

Lead the global Regulatory CMC strategy for a late-stage small molecule programme.
Drive preparation and delivery of the CMC components of a Marketing Authorisation Application.
Act as the CMC regulatory lead for Health Authority interactions, including briefing package development and regulatory responses.
Partner with Technical Development, Quality, Manufacturing and Supply Chain teams to align development activities with regulatory expectations.
Provide strategic direction to CMC dossier preparation and technical writing activities.
Identify regulatory risks, perform gap assessments and develop mitigation strategies.
Support global submissions across major and emerging markets.
Represent Regulatory CMC within cross-functional project and governance teams.

What We're Looking For

Significant experience within Regulatory Affairs CMC.
Proven involvement in late-stage development programmes and Marketing Authorisation submissions.
Strong understanding of small molecule development and registration activities.
Experience developing and implementing global CMC regulatory strategies.
Strong knowledge of FDA, EMA and ICH requirements.
Exposure to international markets including China, Japan, Canada or other global regions would be advantageous.
Experience authoring or reviewing Module 3 documentation and managing complex CMC submissions.
Confident communicator with the ability to influence stakeholders across multiple functions and geographies.
Strong project leadership, problem-solving and risk management skills.

Regulatory, RA, affairs, CMC, small, molecule, late, stage, phase, development, module, matrix, leadership, consultant, freelance, interim, lead, manager, strategy, registration

Medical Education Manager

Location: UK (Remote with in-person event commitments)

Position type: Permanent

About Our Client

Our client is a specialist healthcare communications organisation focused on delivering evidence-based news and independent medical education for medical specialists. Operating within the UK pharmaceutical and healthcare ecosystem, they create trusted content, collaborate closely with expert clinicians, and run both digital and in-person education initiatives for defined specialist audiences. Their environment is collaborative, fast-paced and well suited to someone who enjoys combining scientific rigour with practical delivery of impactful educational programmes.

The Opportunity

This Medical Education Manager role gives you the chance to shape independent medical education that genuinely supports clinical practice across multiple therapy areas. You will sit at the intersection of scientific content, adult learning, stakeholder engagement and hands-on project delivery. You will work remotely while building strong relationships with senior clinicians, pharma partners and internal teams, taking ownership of programmes from strategic planning through to execution and evaluation.

Key Responsibilities

• Lead the delivery and execution of independent medical education activities, including webinars, in-person meetings and other learning formats.

• Support the Scientific and Education Director in defining the strategic direction for independent medical education programmes.

• Contribute to annual education planning, including topic selection and audience prioritisation.

• Identify educational needs through needs assessments, scientific insights and stakeholder engagement.

• Horizon scan for new developments in therapeutic areas that may require targeted education.

• Build and maintain effective relationships with key opinion leaders, faculty members and professional societies.

• Analyse programme outcomes using quantitative and qualitative data, generating insights to refine future initiatives.

• Manage end-to-end delivery of independent medical education webinars, including faculty coordination, asset management, live execution and post-event reporting.

• Manage end-to-end delivery of in-person events, including venue identification and booking, logistics and liaison with all relevant stakeholders, including industry partners.

• Identify, approach, brief and coordinate expert KOLs to participate in webinars, podcasts and events.

• Provide content development support to expert participants to ensure scientific clarity and educational impact.

• Lead complex cross-functional educational projects from planning through to execution, managing timelines, budgets, vendors and contracts.

• Write and edit run sheets and scripts for live webinars and events.

• Develop written materials to support medical education, including educational content and learning objectives based on adult learning principles.

• Contribute to proposals and grant applications to secure funding for independent education programmes.

• Create materials to promote educational events, such as email copy and website text.

• Support the recording and editing of content such as webinars, videos and podcasts.

About You

• BSc in medical or related sciences (or equivalent scientific degree).

• Experience delivering projects for pharmaceutical companies or medical communications agencies in the UK.

• Solid understanding of medical science and pharmaceutical marketing/communications.

• Awareness of adult learning principles and how to translate them into effective educational formats.

• Proven medical writing experience, ideally within MedComms/MedEd.

• Demonstrable project management experience, including time and budget management.

• Training in the ABPI Code and confidence working within regulatory and compliance frameworks.

• Experience working with KOLs and external faculty, including briefing and relationship management.

• Strong interpersonal skills, with the ability to communicate clearly and respectfully with clinicians, pharma stakeholders and internal colleagues.

• Comfortable managing a complex workload, problem solving and taking initiative to move projects forward.

• High level of computer literacy, including Microsoft Office and other relevant systems.

• Flexible, solutions-focused and comfortable working within a small, agile business with a collaborative, “can do” mindset.

Who You’ll Work With

• Internally, you will collaborate closely with sales and marketing, partner content teams, the medical education team and editorial colleagues to deliver cohesive programmes.

• Externally, you will engage with medical and marketing personnel in pharmaceutical, biotech and medical device organisations, as well as PR and creative agencies.

• You will also work directly with senior clinicians and healthcare professionals who contribute to educational and commercial content projects.

What This Role Offers You

• The opportunity to directly influence independent medical education that supports real-world clinical decision-making.

• High levels of ownership across programmes, from strategy and design through to delivery and evaluation.

• Regular interaction with leading clinicians, faculty and industry stakeholders.

• A remote-working setup combined with the variety of in-person meetings and events.

• A collaborative culture where your scientific expertise, creativity and initiative are valued within our client’s team.

How to Apply

If you are an experienced MedEd or MedComms professional with a strong scientific background, proven project delivery experience in the UK pharma environment and confidence working with KOLs, we would like to hear from you. Please submit your CV to be considered and we will be in touch to discuss this Medical Education Manager position in more detail.

Senior Regulatory CMC Project Lead - Interim

Late-Stage Small Molecule Development | Global Regulatory Strategy | MAA Preparation

6 months – renewable

Remote

If based in UK, Outside IR35

Are you a seasoned Regulatory CMC professional looking to take ownership of a high-profile late-stage asset approaching registration?

We're supporting an innovative global pharmaceutical organisation seeking a Senior Regulatory CMC Project Lead to drive regulatory strategy for a key small molecule programme as it advances towards Marketing Authorisation submission.

This is a highly visible position where you'll play a central role in shaping global CMC regulatory strategy, influencing critical development decisions, and working alongside senior scientific, quality, supply chain and regulatory leaders across multiple geographies.

The Opportunity

You'll become the strategic Regulatory CMC lead for a late-stage small molecule asset, taking ownership of the global CMC regulatory roadmap and ensuring successful preparation and delivery of the registration dossier.

Working at the heart of a complex global development programme, you'll collaborate with cross-functional teams, lead agency interaction strategies, manage regulatory risk, and help accelerate the path to patients through innovative and pragmatic regulatory approaches.

This is an excellent opportunity for someone who enjoys combining technical CMC expertise with strategic leadership, stakeholder engagement, and regulatory project delivery.

What We're Looking For

10+ years' experience within Regulatory Affairs CMC – focused specifically on small molecule late stage development.
Proven experience leading the CMC components of global Marketing Authorisation submissions.
Strong understanding of late-stage development and registration activities for small molecule products.
Experience developing and executing global regulatory strategies.
Deep knowledge of FDA, EMA and ICH regulatory requirements.
Exposure to international markets such as China, Japan, Brazil and Canada would be highly advantageous.
Demonstrated success working within complex, cross-functional global development teams.
Excellent project leadership, communication and stakeholder management skills.
Strong analytical, problem-solving and risk management capabilities.
Life Sciences degree required; MSc, PharmD or PhD preferred.

CMC, regulatory, MAA, late, phase, three, development, small, molecule, API, BLA, stage, interim, freelance, contract

Senior Director, Engineering & Maintenance

We are partnered exclusively to appoint a Senior Director of Engineering & Maintenance to lead a multi-site pharmaceutical manufacturing organisation through an exciting period of growth, investment and operational improvement.

With responsibility for Engineering, Maintenance, Reliability, Automation, Validation and Capital Projects, this role will focus on strengthening leadership capability, driving engineering performance and ensuring the organisation is equipped to support future expansion.

Leading a team of functional heads and an organisation of 50+ technical professionals, you will balance strategic priorities with operational execution, identifying risks, developing talent and delivering sustainable improvements across multiple manufacturing facilities.

Key Responsibilities

Provide leadership across Engineering, Maintenance, Reliability, Automation and Validation
Drive engineering strategy and site improvement initiatives
Develop and coach technical leaders across the organisation
Support major capital investment and expansion programmes
Strengthen reliability, compliance and risk management practices
Build a culture of accountability, engagement and continuous improvement
Identify capability gaps and implement development plans

Desired Experience

Significant engineering leadership experience within a regulated pharmaceutical manufacturing environment – drug product or drug substance. Sterile/Aseptic would be advantageous.
Must bring previous Director or Senior Director level responsibility – demonstrating exposure to different environments and challenges.
Experience leading multi-disciplinary engineering teams
Strong understanding of maintenance, reliability and validation principles
Background within pharmaceutical, biotech, sterile, aseptic or other cleanroom manufacturing environments
Demonstrated success developing teams and future leaders
Experience supporting growth, transformation and capital projects

Leadership Profile

We're looking for a leader who knows how to build high-performing teams. Someone who can coach, mentor and develop others, whilst creating clear expectations, accountability and engagement across the organisation.

This is an opportunity to join a business investing heavily in its operations and people, offering significant scope to shape the engineering function and make a lasting impact on future growth.

Engineering, maintenance, validation, capex, project, pharmaceutical, manufacturing, reliability, automation, continuous, improvement