Warman O'Brien

About the Company

Warman O'Brien is a global Life Sciences Recruitment partner, working across the UK, Europe, USA, and APAC.

We're proud to say that we have a 90% success rate of CV-to-interview matches, and our partnerships with pioneering Biotech, Pharma, and CROs across the USA, UK, Europe, and APAC. We recruit top talent across multiple functional areas, including Biometrics, Data Science, Quality Assurance, Regulatory Affairs, Clinical Research, Discovery Sciences, and Medical.

Roles we recruit for
Biostatisticians | Statistical (SAS & R) Programmers | MSL | Data Managers | Data Scientists | Bioinformaticians | Software Engineers | Clinical Research Associates | Clinical Project Managers | Translational Research | Product Characterisation | Discovery Sciences | Heads of and Directors of Departments | QA Managers | Qualified Persons | Regulatory Affairs and the C-Level role: CMO, CTO, CEO, COO, CSO.

Geographical Coverage
USA | UK | Europe | APAC

Service Offering
Permanent Recruitment | Contract Recruitment | Executive Search | Project and SOW Delivery

Our constant endeavour has been to effectively build a world leading network of candidates and clients. Since 2005, our consultants have been exhibiting our services and presenting our industry expertise at PhUSE, PSI, PharmaSUG and ASGCT.

info@warmanobrien.com | www.warmanobrien.com | +44 (0) 2033255075

Listed Jobs

Company Name

Warman O'Brien

Job Title

Senior Process Quality Excellence Specialist

Job Description

**Job Title:** Senior Process Quality Excellence Specialist **Role Summary** Provide expertise in SOP development, process improvement, and quality documentation for global pharmaceutical clinical studies. Deliver independent, cross‑functional SOPs and process documentation, supporting governance and risk management initiatives over a 12‑month contract. **Expectations** - 12‑month contract, 2 days per week on site (Slough). - Autonomously produce and revise SOPs aligned with global quality standards. - Collaborate with data management, risk management, and clinical research teams. **Key Responsibilities** - Draft, review, and update SOPs and supporting process documents for clinical studies. - Lead process improvement initiatives targeting efficiency, compliance, and risk mitigation. - Provide guidance and support to stakeholders on SOP application and best practices. - Ensure documentation meets regulatory and internal quality criteria across global programs. **Required Skills** - Extensive SOP writing and documentation experience. - Clinical research and data management knowledge, including risk and data standards frameworks. - Strong analytical and cross‑functional collaboration abilities. - Effective written and verbal communication in English. **Required Education & Certifications** - Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field. - Professional certifications such as GCP, or Quality Management System (QMS) related credentials preferred but not mandatory.

Slough, United kingdom

Hybrid

Senior

25-11-2025