SRG - Hybrid work

CPI seeks a Bid Development Manager to drive public-funded R&D projects in Pharma & HealthTech. This role blends science, innovation, and business development, requiring a scientific degree and experience with InnovateUK or Horizon Europe. Based in Darlington, you will build consortia, identify f...

CPI seeks a visionary Head of Learning & Development to lead its capability strategy in Sedgefield, UK. This high-visibility role involves shaping leadership programmes, building capability frameworks, and evolving learning into a holistic development model. You will lead a specialist team, requi...

Medical Device Regulatory Administrator sought for a growing healthcare organisation in Gosmore, UK. This role supports product safety, quality, and regulatory processes within a collaborative team. Ideal for an organised administrator with document control or compliance experience, offering expo...

Clinical Safety Scientist role in London, UK. You will monitor safety profiles, conduct signal detection, and evaluate clinical trial data. Requires a Life Sciences degree, pharmacovigilance experience, and strong scientific writing skills. Join a team ensuring regulatory compliance for global sa...

Senior Computational Scientist sought in Cambridge, UK. Leverage your PhD/MSc in Bioinformatics and proven expertise in R/Python to lead algorithm and pipeline development. Drive innovation by analyzing large-scale NGS, genomic, and clinical datasets. This role offers the chance to create novel c...

Regulatory Specialist role in Essex with a leading specialty polymers manufacturer. Join a close-knit compliance team ensuring global chemical regulation adherence. Ideal for candidates with REACH, GHS, and SAP EHS experience, managing safety data sheets and product data. Offers a clear career st...

We are seeking a detail-oriented QMS Support Specialist for a 6-month contract with a leading pharmaceutical company in Harlow, UK. This role is vital for ensuring documentation accuracy and compliance within a regulated GMP environment. Key responsibilities include managing controlled documents ...

Regulatory & Quality Manager sought for a rapidly growing London-based consumer goods company with a Class I medical device portfolio. This role leads the QMS to ISO 13485 and 21 CFR 820, managing compliance, audits, and regulatory submissions. Ideal candidates have 7+ years in medical device QA/...

SRG is seeking a Manufacturing NPD Engineer in Cambridgeshire to lead new product development and seamless scale-up to production. This role demands proven NPD/NPI experience, strong manufacturing process knowledge, and excellent project management skills. You will collaborate with R&D, quality, ...