Permanent recruitment across the technical, regulatory and commercial roles that run UK life sciences.
Outside this list, ask. Our network reaches further than the page, and we will tell you straight whether we are the right partner.
RA managers, EU and UK QPPVs, regulatory submissions specialists, MDR / IVDR leads, CTA and CTIS specialists, RA directors, post-Brexit RA leads.
Clinical project managers, CRAs, clinical operations directors, study managers, clinical trial leaders, CRO oversight specialists, GCP auditors.
QA managers, GMP / GCP / GLP auditors, ISO 13485 specialists, QPs, validation leads, deviation and CAPA specialists, quality systems managers.
Manufacturing managers, production scientists, cleanroom team leaders, scale-up engineers, technical transfer leads, fill / finish specialists.
Design assurance engineers, medical device R&D leads, design transfer specialists, MDR remediation leads, post-market surveillance managers.
Process development scientists, formulation chemists, downstream / upstream process specialists, biotechnology engineers, scale-up scientists.
PV specialists, drug safety officers, ICSR processors, signal detection scientists, EU QPPVs, aggregate reports specialists, PV physicians.
MSLs, medical advisors, medical directors, medical communications specialists, scientific affairs leads, real-world evidence scientists.
Brand managers, key account managers (NHS / private), market access managers, health economics specialists, commercial directors, BD managers.
HSE managers in pharma / biotech, environmental compliance leads, GxP compliance officers, data integrity specialists, validation engineers.
Bioinformaticians, biostatisticians, clinical data managers, programmers (SAS / R), real-world data scientists, data engineers in life sciences.
Heads of R&D, VPs Operations, Directors of Quality, Heads of Regulatory, CSOs, Site Heads, GM-track searches in life sciences.
The specialism shapes part of the workflow, but most of it is the same. Whether the role is a Qualified Person at a pharma manufacturing site or an MSL covering a niche therapeutic area, we follow the same methodical process so nothing slips.
If it is a regulatory role, we know your therapeutic area's submission landscape. If it is QA in pharma manufacturing, we know what data integrity looks like in audit. We come prepared, not script-reading.
Every shortlist is calibrated against current UK life sciences salary data plus what we are seeing live across the desk this month. Sponsor-experience differentials, GxP loading, and London / Cambridge / Northern hub deltas all factored in.
Three to five candidates per brief. ICH-GCP, EU GMP, NEBOSH where relevant, and right-to-work confirmed before introduction. Each ranked against the brief with a written note on regulatory background and motivation.
We coordinate the offer, manage counter-offer pressure, line up the start date and any pre-employment screening, and check in at week 2, 6 and 12.
Clinical-bedside healthcare, pure academic research, very junior individual contributors, and senior corporate executive search above £200k base sit best with sector specialists. We will refer rather than try to compete.