SRG

About the Company

SRG are industry leaders in Life Sciences, Clinical and Engineering Recruitment and the largest Life Science recruitment agency in the UK. With over 30 years’ experience of helping leading STEM organisations find, hire and retain the very best STEM talent, we understand what job seekers and employers are looking to achieve, and what they need to get there.

At SRG, our industry experts draw on their own experience, technical and scientific backgrounds and expertise, and work in partnership with businesses to ensure hiring success in any role – for all levels of experience, no matter how niche.

We believe collaboration and flexibility is key to creating impactful staffing and recruiting solutions that will not only help people and businesses unlock their potential but help build a brighter future for STEM too.

SRG is part of Impellam Group, a connected group providing integrated global workforce and specialist recruitment solutions.

Listed Jobs

Company Name

SRG

Job Title

Associate Director

Job Description

Job title: Associate Director – Evidence Generation Role Summary: Lead the design, execution, and interpretation of real‑world evidence (RWE) and non‑interventional studies that inform access, adoption, and patient outcomes for innovative therapies. Manage cross‑functional teams and external stakeholders, ensuring scientific rigor and relevance while capitalising on advanced data science and novel research methods. Provide strategic direction and regulatory insight throughout the evidence lifecycle. Expactations: - Minimum 5 years of evidence generation or RWE experience in pharma, biotech, academia or healthcare. - Advanced degree in Life Sciences, Public Health, PharmD, MD, MSc, or PhD (MBA preferred). - Proven leadership in global, cross‑functional projects with KOLs and patient groups. - Strong analytical and scientific communication skills to influence diverse audiences. - Demonstrated ability to innovate and adopt emerging data‑science techniques. Key Responsibilities: - Design and execute observational and RWE studies aligned with Integrated Evidence Plans. - Develop protocols, analysis plans, and deliverables, contributing to scientific publications and conference presentations. - Ensure methodological rigor and relevance of evidence strategies, study design, and data interpretation. - Lead collaborations with internal teams, KOLs, patient advocacy groups, and advisory boards to produce robust evidence outcomes. - Represent the organisation in external collaborations, steering committees, and regulatory discussions. - Champion advanced data‑science and novel research methodologies to enhance evidence generation. - Stay current on regulatory and industry developments in RWE and observational research. Required Skills: - Observational study design & epidemiology - Data interpretation & real‑world data (RWD) analytics - Bioinformatics / data science proficiency - Stakeholder engagement & cross‑functional leadership - Scientific writing and presentation - Strategic thinking and organisational leadership - Innovation, people management, and project coordination Required Education & Certifications: - Advanced degree in Life Sciences, Public Health, PharmD, MD, MSc, or PhD; MBA preferred. - Minimum 5 years of evidence generation or RWE experience in pharmaceutical, biotech, academic or healthcare settings. - Familiarity with HEOR, RWE guidance, and regulatory requirements for observational research.

England, United kingdom

Hybrid

Mid level

29-10-2025

Company Name

SRG

Job Title

Validation Specialist

Job Description

**Job title:** Validation Specialist **Role Summary** Develop, optimize, and validate analytical methods for compound identification and quantification. Ensure methods meet GMP and industry standards, support R&D projects, troubleshoot instrumentation, and maintain accurate documentation. **Expectations** * 12‑month contract, with potential for extension. * Deliver validated methods that meet accuracy, precision, and consistency requirements. **Key Responsibilities** 1. Design, develop, and refine analytical methods using technologies such as HPLC, GC, KF, and spectroscopy. 2. Execute method validation studies: accuracy, precision, specificity, linearity, range, detection and quantitation limits, robustness, and system suitability. 3. Collaborate with R&D teams to understand project goals and provide analytical support. 4. Troubleshoot method, instrument, and data‑analysis issues. 5. Keep up-to-date with emerging analytical techniques and propose process improvements. 6. Prepare and maintain documentation: method development reports, validation protocols, standard operating procedures, and regulatory files. **Required Skills** * Proven experience in laboratory setting with analytical method development and validation. * Proficiency in HPLC, GC, KF, UV‑Vis, fluorescence, MS, or related spectroscopy techniques. * Strong analytical and problem‑solving abilities. * Excellent written and verbal communication for documentation and cross‑functional collaboration. * Understanding of GMP requirements and analytical validation regulations (e.g., FDA, EMA). **Required Education & Certifications** * Bachelor’s or Master’s degree in Microbiology, Chemical/Analytical Chemistry, Biochemistry, or related scientific discipline. * Familiarity with GMP standards and analytical method validation guidelines.

Derbyshire, United kingdom

On site

05-11-2025

Company Name

SRG

Job Title

Laboratory Technician

Job Description

**Job Title** Laboratory Technician – R&D **Role Summary** Perform physical testing for consumer products to support the EMEA R&D team, ensuring compliance with the Quality Management System (QMS). Execute tests, maintain equipment, and manage documentation, while applying 5S and LEAN principles to improve laboratory processes. **Expectations** - Work safely under Northfleet Mill Safety Policy. - Follow client QMS and industry standard test methods. - Deliver accurate, timely test results and reports. - Maintain and calibrate equipment per schedule. - Support in‑mill trials and inter‑EMEA collaboration. - Contribute to continuous improvement initiatives. **Key Responsibilities** 1. Conduct physical tests (competitor audits, RSRs/MSRs, ad hoc requests, correlation checks). 2. Record and report data in designated formats or customer‑specified forms. 3. Perform regular equipment verification and calibration. 4. Maintain archived records and product samples. 5. Apply 5S housekeeping and LEAN principles to laboratory workflow. 6. Provide trial support across EMEA locations as needed. 7. Communicate results and issues clearly to team members and stakeholders. **Required Skills** - Attention to detail and thorough cross‑checking. - Structured and organized document/record management. - Ability to work autonomously and within a small team. - Effective written and verbal communication. - Flexibility to adapt to changing priorities. - Proficiency in Microsoft Office, SharePoint, and relevant systems/databases. **Required Education & Certifications** - Minimum of 5 GCSEs (A–C grades) including Maths and English **or** one year of experience in a similar laboratory role.

Northfleet, United kingdom

On site

Fresher

25-11-2025

Company Name

SRG

Job Title

Materials Characterisation Scientist

Job Description

**Job Title:** Materials Characterisation Scientist **Role Summary:** Conduct experiments to characterize and compare different suppliers of active pharmaceutical ingredients (APIs) using analytical techniques (particle size analysis, microscopy, SEM, thermal analysis, solid form identification, spectroscopy, powder flow & density). Use data to assess manufacturing risks and produce technical reports. **Expectations:** - Work independently and document results clearly. - Meet strict timelines while managing multiple priorities. - Communicate findings effectively in written reports and presentations. **Key Responsibilities:** - Design and execute laboratory experiments for material characterization. - Perform experiments in accordance with GLP, SOPs, and established processes. - Document laboratory work in a detailed, clear, and timely manner. - Summarize results in a technical report. - Participate in laboratory practices, including My Green Lab and 5S initiatives. **Required Skills:** - Independent work and strong self‑direction. - Excellent oral and written communication, with emphasis on clarity. - High attention to detail and ability to follow departmental procedures. - Pro‑active, highly motivated, and comfortable in a fast‑paced environment. - Interpersonal skills to collaborate with personnel at all levels. **Required Education & Certifications:** - Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related scientific field. - 1–2 years of relevant experience in materials characterization or related laboratory work.

Sandwich, United kingdom

On site

25-11-2025