SRG

Join a global pharmaceutical leader in London as a Regulatory Affairs Training Manager. You will be the SME for Veeva RIM rollout, designing and delivering training to RA staff and Super Users. This role requires strong project management, Veeva RIM experience, and expertise in creating impactful...

Join a global biopharmaceutical CDMO as a Laboratory Technician in Slough. Utilize your scientific degree and cell culture skills in a dynamic R&D environment. Your role will include lab maintenance, buffer prep, and supporting bioreactor operations. Strong organization and teamwork are essential...

Join a leading biopharma manufacturer as an MSAT Bioprocess Specialist in Falkirk. Lead technology transfer and scale-up of biologics into GMP manufacturing. Utilize your process engineering and GMP documentation skills within a robust Quality Management System. Enjoy a competitive package and be...

Lead the electrical design function for cutting-edge capital projects in this senior remote role. Drive engineering excellence and technical strategy from concept to commissioning. Guide a growing team, applying hands-on design expertise in AutoCAD/Revit within the life sciences sector. This UK-b...

Lead GMP production projects in Glasgow, ensuring batches meet quality, timeline, and budget targets. Utilize your pharmaceutical manufacturing experience to oversee cleanroom operations and documentation. Drive continuous improvement while collaborating with clients and cross-functional teams in...

Join a global biopharmaceutical CDMO as an R&D Technologist in Cambridge. This lab-based role focuses on molecular biology, mammalian cell culture, and high-throughput DNA assembly. Ideal for a recent Biological Sciences graduate with core molecular biology knowledge. Contribute to cutting-edge p...

Join a leading life sciences company in Falkirk as a QC Analyst. Utilize HPLC and other analytical techniques in a GMP/GxP regulated environment. This shift-based role offers excellent salary, benefits, and development opportunities during a period of exciting growth.

Join a leading healthcare diagnostics firm in Edinburgh as a Regulatory Affairs Officer. You will manage global submissions (FDA, CE, IVDR) and ensure compliance for medical devices. The role requires strong technical writing and expertise in PMA, 510(k), and ISO13485. Enjoy a collaborative, fast...

Join our London-based team as a Medical Writer, specializing in medical aesthetics. You will create clinical educational content for live and virtual training programs, focusing on facial injectables. This role requires 5+ years of experience, including medical aesthetics expertise, and involves ...

Join a leading personal care manufacturer in Portsmouth as a Global Regulatory Technologist. Utilize your 2+ years of industry experience to manage global compliance for UK, EU, FDA & ASEAN markets. Enjoy a hybrid role with private healthcare, bonus, and 33 days holiday in a culture that champion...

Join a leading UK medical device company as a German-speaking Customer Care Specialist. You will be the primary point of contact, managing customer claims and queries with a focus on healthcare. This role requires fluency in German and English, strong analytical skills, and experience in a custom...

Join our QA Technical Support Team in Worthing as a QA Scientist Analyst. Provide vital analytical support for investigations, trials, and validation within a pharmaceutical GMP environment. Utilize your hands-on experience with chromatography and spectroscopy to ensure cGxP compliance. This role...