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

Quality Assurance Associate

Job Description

**Job Title:** Quality Assurance Associate **Role Summary:** Ensure compliance with GMP standards by managing QC testing documentation, coordinating batch consolidation, and supporting quality systems for pharmaceutical products. **Expectations:** - Coordinate batch consolidation for QC Biochemistry and Microbiology to verify compliance with release specifications. - Issue GMP documents and labels to Manufacturing with accuracy and timeliness. - Proactively manage quality records (Deviations, CAPAs, investigations) and support audit preparation. - Drive continuous improvement of quality systems and processes in collaboration with cross-functional teams. - Maintain document archives and ensure training compliance. **Key Responsibilities:** - Audit QC testing activities for Drug Product and Drug Substance batches. - Author, review, and approve GMP documentation. - Liaise with internal stakeholders to resolve data gaps and ensure alignment with timelines. - Prioritize tasks to meet deadlines and support Manufacturing operations. **Required Skills:** - Attention to detail for accurate data entry and documentation. - Proficiency in MS Office (Word, Excel, Outlook, Access). - Database system familiarity. - Strong verbal and written communication. - Risk-based decision-making and prioritization. - Organizational and planning skills. **Required Education & Certifications:** - BSc in Biology or related field (or equivalent experience). - Entry-level experience (0–4 years); prior QA/GMP experience preferred.

Slough, United kingdom

On site

Fresher

17-09-2025

Company Name

SRG

Job Title

Document Controller

Job Description

**Job Title:** Document Controller **Role Summary:** Manage the Veeva Quality Docs (VQD) system as the designated process owner, providing technical oversight, user support, and compliance with GxP documentation standards. Coordinate documentation lifecycle management, train users, and act as the archives liaison for documentation queries. **Expectations:** 9-month contract with potential extension; on-site work required for VQD system governance, user training, and compliance assurance. **Key Responsibilities:** - Oversee VQD system as process owner and superuser, ensuring system functionality and compliance. - Provide training and technical support for document creation, workflow management, and metadata accuracy. - Resolve system issues related to document types, workflows, access, and retention. - Administer controlled printing and document lifecycle processes, including periodic reviews and deletions. - Track and report on documentation KPIs to ensure system performance. - Coordinate with learning and development teams on myLearning and LSOP alignment. - Act as Archives Champion, managing preservation notices, capacity monitoring, destruction protocols, and archive GMP compliance. - Participate in system forums and access reviews for user management. **Required Skills:** - Veeva Quality Docs (VQD) system administration and troubleshooting. - Training and user support skills for technical software platforms. - Workflow management and GxP/GMP compliance expertise. - Data management and KPI analysis for process improvement. - Interpersonal communication for cross-functional collaboration. **Required Education & Certifications:** - SVQ Level 3, Highers, Higher National Certificate (HNC), apprenticeship, or equivalent qualification.

Montrose, United kingdom

On site

17-09-2025

Company Name

SRG

Job Title

Quality Assurance Manager

Job Description

**Job title** Quality Assurance Manager **Role Summary** Lead and manage all Quality Assurance functions within a GMP/GLP environment, ensuring compliance with cGMP, cGLP, and data integrity standards. Oversee daily QMS operations, drive continuous improvement, and manage validation and audit activities. **Expectations** - Deliver measurable quality targets and KPIs. - Provide effective leadership and training to the QA team. - Maintain up‑to‑date knowledge of regulations and industry best practices. **Key Responsibilities** - Manage the pharmaceutical Quality Management System and daily QA activities. - Ensure compliance with cGMP, cGLP, and data integrity requirements. - Lead and coordinate internal, regulatory, and customer audits. - Oversee method validation, method transfer, and improvement initiatives. - Drive continuous improvement across the site. - Manage staff training on quality practices and compliance. - Report and communicate technical quality data to stakeholders. **Required Skills** - Strong knowledge of GMP/GLP regulations and QA best practices. - Proven leadership and team‑management abilities. - Excellent communication and interpersonal skills. - Analytical mindset with ability to interpret technical data. **Required Education & Certifications** - Degree or equivalent qualification in a relevant scientific field (e.g., Pharmaceutical Sciences, Chemistry, Biology). - Prior senior QA experience in a GMP/GLP setting. ---

Derbyshire, United kingdom

On site

18-09-2025

Company Name

SRG

Job Title

Medical Information Specialist

Job Description

Job Title: Medical Information Specialist Role Summary: Deliver expert, unsolicited medical and scientific support across a full product portfolio, ensuring compliance with pharmaceutical legislation and facilitating informed decision‑making for internal and external stakeholders. Expectations: - Maintain high‑quality MI services that meet ABPI, P3, and GxP standards. - Act as a therapy‑area product expert, driving engagement and innovation across cross‑functional teams. - Continually improve MI processes, KPIs, and customer satisfaction. Key Responsibilities: - Respond to medical/scientific queries from doctors, patients, and internal teams in a timely, accurate manner. - Develop and deliver DOF, SmPC, and product training material for new associates. - Compile and disseminate monthly therapeutic‑area insights; contribute to medical meetings and insight sharing. - Coordinate with Field Medical colleagues to support external engagement and pilot initiatives. - Localise global guidance documents, lead on innovative pilots, and represent the local team at the global level. - Manage adverse drug event reporting and product quality complaints within required timelines. - Ensure MI processes for pipeline launches are robust, inspection‑ready, and aligned with business goals. - Collaborate across PV, TMO, Regulatory, Quality, and Vendor Management to keep information accurate and up‑to‑date. - Identify process optimisation opportunities, reduce low‑value activities, and support digital data system enhancements. Required Skills: - Exceptional written and verbal communication with diverse stakeholders. - Strong project‑management ability with meticulous attention to detail. - In‑depth knowledge of ABPI & other pharma regulatory frameworks (data privacy, copyright). - Solid understanding of healthcare systems and external stakeholder management. - Cross‑functional collaboration, multitasking, prioritisation, and a customer‑focused mindset. Required Education & Certifications: - Bachelor’s degree in Pharmacy or Life Sciences (or equivalent). - Current completion of ABPI / P3 compliance training.

London, United kingdom

Hybrid

19-09-2025