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Enabling CDMOs Growth and Success
Supporting Growth Across Small Molecule, Biologics and Cell & Gene Therapy
Scaling CDMO Teams for a New Era of Manufacturing
The CDMO industry is growing fast, with forecasts putting it on track to surpass $315 billion by 2030. As pharma and biotech companies continue to outsource development and manufacturing, the pressure is on to deliver faster, more cost-effective, and more flexible solutions. North America and Europe remain central to this shift, the US leading the way in biologics and cell & gene therapy, while countries like Germany, Switzerland, and the UK double down on GMP manufacturing capabilities.
We work closely with CDMOs across small molecule, biologics, and advanced therapy platforms. As demand rises and timelines tighten, these organisations need access to highly skilled technical professionals, not just to fill roles, but to keep pace with regulatory change, operational complexity, and global scale-up efforts.
Across both the US and Europe, we’re seeing major investment in new sites, cutting-edge technology, and expanded capacity. But at the heart of it all is one thing: people. No matter how advanced the equipment or how ambitious the growth plans, it’s the teams behind the work that determine success. The right talent brings more than technical execution, it fuels innovation, maintains compliance, and keeps operations running efficiently at scale.
Some of the most in-demand roles across the CDMO space right now include Process Development Scientists who can fine-tune yields and ensure smooth tech transfer between sites, and MSAT specialists who sit at the intersection of R&D and manufacturing, making sure what works in the lab can be scaled compliantly on the floor.
There’s also growing demand for QA/QC and Regulatory Affairs professionals who know their way around global frameworks and can confidently guide programs through inspections and audits. And on the operational side, Manufacturing Engineers and Plant Leaders with hands-on GMP experience and a systems-thinking approach are playing a huge role in helping CDMOs scale up without compromising on quality.
Attracting and keeping hold of this level of specialist talent is quickly becoming a competitive advantage in itself. It’s what allows CDMOs to stay audit-ready, meet the expectations of their partners, and continue growing in a fast-moving, highly regulated market.
Formulation Development
Quality Assurance
Process Development & Optimization
Regulatory Affairs & CMC
Supply Chain Management
Clinical Trial Manufacturing & Packaging
Biomanufacturing
Technology Transfer Solutions
End-to-End Commercial Manufacturing
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Our Specialist Industries
Pharmaceuticals & Biotech
This world is a complex one. Scaling biotechs, established players and CROs all make up a diverse landscape. We’re committed to promoting opportunity, finding talent and driving the industry forward.
Medical and Health Technology
Devices, diagnostics and digital health. The rate of innovation and progression in this sector affects us all and we help you to make a difference by providing the insight, expertise, and people to accelerate its progression.
Healthcare Communications
Making the complicated, accessible. From the large PR agencies to niche, disruptive companies, we partner with those who bring the stories of Life Sciences to life whilst adding our own insight.
CRO & CDMO
In the highly regulated and scientifically complex world of CROs and CDMOs, having the right people in the right roles is critical to delivering for clients, meeting compliance standards, and driving innovation.
Venture Capital & Private Equity
We work directly with VC & PE firms and the companies they invest in to solve some of the toughest talent challenges. From building a leadership team post-investment to supporting rapid hiring through a growth phase.
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Our Life Sciences Talent Solutions
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