Cpl Life Sciences

About the Company

At Cpl UK Life Sciences, we're experts at connecting talented professionals with the most ambitious companies in the industry. With excellent local knowledge of markets across the UK, Switzerland, and the USA, you can trust us to help with all your life science recruitment.

We cover:
- UK
- Switzerland + Europe
- USA

From big pharma, CROs to small biotech start ups, we can deliver the total talent solutions you need.

- Permanent
- Contract/temporary
- FSP
- Embedded (multi-hire)
-Executive Search

Our team has an acute understanding of all life sciences functions. We provide talent and staffing solutions across a range of pharmaceutical disciplines including: clinical, pharmacovigilance, regulatory affairs, commercial, medical communications, and engineering.

We are an award winning staffing agency, with a strong commitment to EDI, and sustainability. Our mission is to be the UK’s best sustainable talent partner across all our core markets, adding meaningful value to lives of our clients, candidates and colleagues.

Listed Jobs

Company Name

Cpl Life Sciences

Job Title

Guidewire Developer

Job Description

**Job Title**: Guidewire Developer **Role Summary**: Design, develop, and maintain customizations and integrations for Guidewire ClaimCenter using Gosu. Collaborate with stakeholders, conduct unit testing, troubleshoot issues, and keep solutions aligned with industry best practices. **Expectations**: Minimum 3 years of experience with the Guidewire Insurance Suite; strong expertise in ClaimCenter configuration and development; ability to work independently in a remote environment; strong communication and problem‑solving skills. **Key Responsibilities**: • Configure and develop ClaimCenter components (workflows, rules, data models) using Gosu • Gather and analyze business requirements with analysts and stakeholders • Design, implement, and integrate custom solutions within ClaimCenter • Create and run unit tests, participate in code reviews, and ensure coding standards • Troubleshoot and resolve platform‑related issues • Collaborate with QA to support testing and defect resolution • Provide technical guidance to team members and stakeholders • Stay current with Guidewire product releases and industry trends **Required Skills**: • Guidewire Insurance Suite (ClaimCenter) – 3+ years • Gosu programming language – 3+ years • Configuration and development of ClaimCenter workflows, rules, data models • Unit testing, debugging, and troubleshooting in Guidewire • Code review and adherence to best practices • Strong analytical and communication skills **Required Education & Certifications**: • Bachelor’s degree in Computer Science, Software Engineering, or related field (preferred) • Guidewire ClaimCenter developer certification (preferred, but not mandatory)

United kingdom

Remote

05-11-2025

Company Name

Cpl Life Sciences

Job Title

Software Dev Engineer

Job Description

Job Title: Software Development Engineer Role Summary: Deliver software solutions that drive operational efficiencies and improve key fulfillment KPIs across a global network. Work on workstation and mobile applications, real‑time dashboards, and automation tools, partnering with product, ops, and engineering stakeholders. Expectations: - Independently design, develop, test, and deploy applications in a hybrid IT environment under IR35. - Influence scaling KPIs such as manual effort, response time, cost, and throughput. - Collaborate cross‑functionally and translate business requirements into executable technical designs. Key Responsibilities - Design and build applications for fulfillment workstations and mobile devices. - Develop web tools and dashboards to optimize resource utilization and operational processes. - Enhance services managed by Ops engineering (e.g., Amazon Fulfillment Technologies). - Standardize processes, reduce manual touchpoints, and increase overall efficiency. - Implement automation to lower manual effort and accelerate response times. - Analyze business needs, produce detailed low‑level designs, and lead implementation. - Engage product managers, ops teams, and peers to deliver clear business solutions. Required Skills - Strong programming in Python and Java; experience with Scala/other modern OOP languages preferred. - Front‑end development with React and either JavaScript or TypeScript. - Cloud computing experience, preferably AWS. - Ability to collaborate with technical and non‑technical stakeholders. - Autonomous, proactive problem‑solving and project ownership. Required Education & Certifications - Bachelor’s degree in Computer Science, Software Engineering, or a related field. - AWS Cloud Practitioner or related certification desirable but not mandatory.

London, United kingdom

Remote

20-11-2025

Company Name

Cpl Life Sciences

Job Title

EU Senior Regulatory Affairs Manager / FTC

Job Description

**Job Title:** EU Senior Regulatory Affairs Manager – FTC **Role Summary:** Lead EU regulatory strategy for drug development in respiratory and inflammation, overseeing clinical trial submissions, CTR applications, PIPS, and MAA processes, while monitoring evolving EU legislation and ensuring compliance. **Expectations:** - 12‑month fixed‑term contract. - Must start within 4 weeks of offer. - Based in the UK or Ireland with full right to work. **Key Responsibilities:** - Develop EU‑aligned regulatory strategies for early‑ and late‑stage clinical programs. - Lead clinical study start‑up, CTR submissions, PIPS activities, and manage agency queries and compliance issues. - Oversee MAA‑related strategy and processes to secure timely approvals with differentiated labeling. - Monitor emerging EU legislation and guidance, ensuring organisational awareness and compliance. - Represent the EU regulatory function to EMA, national agencies, and alliance partners. **Required Skills:** - Deep knowledge of EU clinical research regulations (CTR, EMA, national guidelines). - Proven ability to manage multiple regulatory projects simultaneously. - Strong written and verbal communication, stakeholder management, and organizational skills. **Required Education & Certifications:** - Advanced science degree (Master’s or Ph.D.). - Minimum 5 years regulatory affairs experience in drug development, including CTA submissions. - Preferred: cell‑therapy experience and demonstrated EU strategy leadership.

Uxbridge, United kingdom

Hybrid

Senior

22-12-2025

Company Name

Cpl Life Sciences

Job Title

Managing Device Lifecycle Asset Management

Job Description

Job title: Managing Device Lifecycle Asset Management Role Summary: Own the end‑to‑end lifecycle of corporate mobile devices across Europe, from planning and procurement to provisioning, support, compliance, reverse logistics, and responsible disposition. Deliver seamless operations, maintain accurate asset records, and ensure SLA compliance. Expectations: • Deliver consistent, high‑quality service and meet all device‑management SLAs. • Proactively forecast demand, manage inventory, coordinate shipments, and resolve escalations. • Maintain compliance with security, privacy, and regulatory requirements. • Communicate effectively with associates, hiring managers, carriers, logistics partners, and internal stakeholders. Key Responsibilities: • Forecast demand, manage stock levels, raise requisitions, and coordinate with carriers/warehouses for timely delivery. • Triage support requests via “My Mobile,” enforce policies, and manage service requests, faulty returns, and replacements. • Track device lifecycle states, perform secure erasures, and maintain compliance records. • Oversee reverse logistics: field return QA, routing for repair/reuse, inventory replenishment, or environmentally responsible recycling. • Partner with logistics providers to streamline reverse‑logistics flow and ensure efficient disposal. • Coordinate with carriers, logistics partners, and internal teams; participate in onboarding and strategy forums. Required Skills: • Attention to detail, strong organizational abilities. • Excellent written and verbal communication. • Self‑starter with the ability to work independently. • Presentation and confidence in stakeholder interactions. • Critical thinking and creative problem‑solving. • Prioritization and time‑management to meet deadlines. • Vendor management and communication skills. • Detail orientation to compliance and asset accuracy. • Device lifecycle management experience. • Knowledge of Microsoft Intune, Apple Business Manager, and ServiceNow. Required Education & Certifications: • High‑school diploma or equivalent. • Relevant certifications in device management (e.g., Microsoft Certified: Modern Desktop Administrator Associate, Apple Certified Support Professional) preferred.

Northwich, United kingdom

On site

19-01-2026