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We’re supporting a global life sciences organisation in the search for an experienced Clinical Supply Chain Logistics professional to provide end-to-end logistics oversight for clinical trial supply programs. This role focuses on ensuring the timely delivery of Investigational Medicinal Products (IMP) to support key clinical milestones while coordinating closely with study teams and external partners. Key Responsibilities • Act as the primary logistics contact for assigned clinical studies, • Oversee Stock Transfer Orders (STOs) and global shipment execution, • Monitor and manage urgent or priority clinical shipments, including temperature-sensitive supplies, • Coordinate with study teams, supply managers, and external partners (CMOs, depots, logistics providers), • Identify and resolve logistics risks, delays, or supply issues, • Provide status reporting, risk tracking, and escalation during critical study phases Requirements • Degree in Supply Chain, Life Sciences, Engineering, or related field, • Experience in clinical supply chain or clinical trial logistics, • Strong experience with shipment execution and STO management, • Ability to work in fast-paced, time-critical environments, • Excellent stakeholder communication and organisational skills About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

🚀 Quality Assurance Officer – North Merseyside 💰 Up to £35,000 | 🏭 Pharma / Life Sciences Manufacturing We’re partnering with a specialist life sciences manufacturer as they expand their QA team. If you’re detail‑driven, GMP‑savvy and ready for a role where quality truly matters, this one’s worth a look. 🔍 What You’ll Be Doing • Owning SOPs and quality documentation, • Supporting internal & external audits, • Driving improvements across ISO 9001, GMP & MHRA compliance, • Reviewing lab, calibration & QA records, • Investigating deviations, NCRs & customer complaints 🎓 What You’ll Bring • Strong GMP experience - at least 2 years industry experience, • QA background (or QC with QA exposure), • Solid understanding of deviations/NCRs, • A BSc or MSc in a Scientific subject, • Sharp attention to detail and a proactive mindset 💼 Why It’s a Great Move • Salary up to £35k, • Join a respected, specialist life sciences organisation, • Supportive QA leadership and real scope to influence improvements Please note: My client is unable to offer sponsorship for this role. 📩 Interested? Reach out to Nexus Life Sciences for a confidential chat or send your CV directly.

Senior Quality Associate – Senior Third Party Quality Assurance Specialist 📍 Speke, United Kingdom | Full Time | Quality Assurance Contract length: 12 months with a high chance of extension FTE: Full time 37.5 hours/week Onsite presence- 3 days in office, 2 days wfh An established, global pharmaceutical company is seeking a Senior Quality Associate (Senior Third Party Quality Assurance Specialist) to join its Europe, Emerging Markets and Middle East Quality team based in Liverpool. This organisation develops and manufactures products worldwide with a strong international footprint and science-led approach, it offers a collaborative environment, high regulatory standards, and genuine opportunities for professional development within a growing global business. The Role This position plays a key role in overseeing third-party manufacturers and ensuring externally manufactured products are produced and released in line with Good Manufacturing Practice requirements, regulatory expectations, and internal quality standards. You will operate and maintain quality systems that monitor supplier compliance, proactively manage risk, and support uninterrupted product supply across multiple regions. Key Responsibilities • Provide quality assurance oversight of assigned external suppliers and third-party manufacturers, • Monitor supplier performance metrics to proactively identify and escalate compliance risks, • Review and assess customer complaints, including root cause investigations, product impact assessments, trend analysis, and corrective and preventive actions, • Review third-party deviation reports for completeness, investigation quality, impact assessment, and corrective actions, • Review batch release documentation and support product release activities, including material status updates within enterprise resource planning systems, • Review Product Quality Reviews and assess supplier-level quality trends, • Ensure annual pharmacovigilance statements are obtained and reviewed, • Maintain effective third-party quality systems, including quality agreements and supplier risk assessments, • Represent Quality Assurance within cross-functional projects and support quality management as required About You • Scientific degree in Chemistry, Biology, Pharmacy, Pharmaceutical Engineering, or a related discipline, • Experience within a Good Manufacturing Practice quality environment, • Strong background in deviations, complaints, investigations, and corrective and preventive actions, • Understanding of regulatory requirements within a pharmaceutical or health setting, • Familiarity with enterprise resource planning systems and structured quality management systems, • Experience overseeing third-party manufacturers or external partners is highly desirable, • Exposure to working within a global organisation would be advantageous If you would like to discuss this vacancy further or to discuss your career options in confidence, please contact Femi Olubodun via telephone on +44 (0) 2039288387 or email on: If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! About Planet Pharma Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

About the Role We are seeking an experienced Clinical Supply Chain Logistics Specialist to support global clinical trial programs during critical operational phases. This role focuses on providing end-to-end logistics oversight to ensure uninterrupted delivery of Investigational Medicinal Product to clinical sites and patients. Operating in a hyper-care environment, you will play a key role in monitoring and driving shipment execution, resolving logistics issues, and ensuring supply continuity during time-sensitive milestones such as study start-up, major transfers, and database lock. You will act as the primary logistics point of contact for assigned studies, coordinating closely with clinical study teams, trial supply managers, regional delivery leads, and external partners. Key Responsibilities Clinical Supply Logistics Oversight • Provide operational oversight of logistics activities for assigned clinical supply programs., • Monitor and manage Stock Transfer Orders across internal and external networks., • Act as the primary logistics interface for study teams and supply chain stakeholders., • Support alignment between clinical supply priorities, patient enrollment needs, and trial milestones., • Track shipment progress and proactively intervene in the event of delays, deviations, or risks., • Coordinate urgent or temperature-sensitive deliveries and prioritize shipments where required., • Coordinate with external partners such as CMOs, packagers, and depots to monitor transfer timelines and release readiness., • Provide regular reporting on logistics performance, shipment execution, and STO health., • Maintain visibility of critical risks, open issues, and escalation points., • Bachelor’s degree in Supply Chain, Life Sciences, Engineering, or a related discipline., • Experience in clinical supply chain logistics within a pharmaceutical, biotech, or CRO environment., • Strong experience managing shipment execution, supply transfers, and issue resolution within global clinical trials., • Familiarity with working with external partners such as CMOs, depots, and logistics providers., • Ability to work effectively in high-pressure, time-critical operational environments., • Strong organizational, problem-solving, and stakeholder management skills., • Excellent communication skills and the ability to coordinate across global teams.

I’m currently supporting a global pharmaceutical organisation known for its innovation in clinical development and strong commitment to quality and patient safety. This is a great opportunity to join a highly regulated, fast-paced environment where you’ll play a key role in ensuring clinical trial materials are managed, stored, and distributed efficiently and compliantly. Key responsibilities: • Manage goods receipt, sampling, storage, dispensing, and dispatch of clinical trial materials, • Ensure all warehouse and dispensary activities are conducted in line with GxP, EHS, and SOP requirements, • Execute materials and warehouse management transactions within SAP, • Maintain compliance with transport security, COSHH regulations, and hazardous goods legislation, • Support internal audits and regulatory inspections, • Liaise closely with Quality teams to ensure approvals, traceability, and chain of custody, • Operate counterbalance and reach forklift trucks safely within a regulated environment Requirements: • Experience in materials management or logistics, ideally within a pharmaceutical or regulated environment, • Working knowledge of GxP guidelines, • RTITB qualification for reach and counterbalance forklift trucks, • Experience handling and transporting hazardous goods, • Strong IT skills, including SAP and Microsoft Office, • Excellent communication skills with the ability to build effective working relationships, • Proactive, flexible, and team-oriented approach About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

Our client, a global pharmaceutical company, is currently looking for a Clinical Supply Chain Logistics Manager to join their team near Liverpool on a full time, 12-month temporary basis. This role ensures investigational medicines are delivered to study sites on time, supporting key clinical milestones and patient needs. You will act as the central point of contact for logistics activities, coordinating with study teams, supply managers, regional leads, and external partners to ensure shipments move efficiently across global networks. Key Responsibilities • Oversee day-to-day logistics operations for clinical supply programs., • Monitor stock transfer orders and ensure timely shipment execution., • Track shipments and proactively resolve delays or supply risks., • Coordinate urgent and temperature-sensitive deliveries., • Work closely with external partners including CMOs, depots, and logistics providers., • Provide regular updates on shipment status, risks, and priorities. Requirements • Degree in Supply Chain, Life Sciences, Engineering, or similar., • Experience in clinical supply chain logistics within pharma or clinical trials., • Strong organisational skills and ability to manage urgent priorities., • Excellent communication with global teams and external partners. Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.

The Setup: A high-growth agile unit within the global STARLIMS ecosystem. STARLIMS provides leading Laboratory Information Management System (LIMS) solutions that have served customers around the world for over 30 years. Our solution suite helps labs: • Improve the reliability of sampling and testing, • Manage complex testing workflows and analytical methods, • Support compliance with global regulatory requirements and industry standards The Role: Architect, Mentor, & AI Pioneer We are looking for a Senior Architect/Lead Developer to take complete ownership of the Labstep platform. You will be the primary decision-maker for our architecture, moving us from a robust data tool to an AI-augmented powerhouse. The Opportunity: The Best of Both Worlds Labstep was founded to build user-centric software that accelerates scientific discovery. Recently, we joined forces with STARLIMS, a global leader in Informatics. What this means for you: You get the high-impact, fast-moving "Day 1" culture of a startup where you own the entire tech stack, backed by the job security, comprehensive healthcare, and professional benefits of a major global organization. • Complete Technical Autonomy: You own the AWS-based stack (Pulumi, ECS, Fargate). You decide the "how" and the "when" for every major architectural shift., • Lead the AI Roadmap: You will architect our AI Search and Natural Language Agent. We want a pragmatic engineer who can lead the implementation of LLMs and Vector Databases to help scientists automate complex tasks., • Mentorship & Team Lead: You will work closely with a Technical Product Manager and mentor a Junior Developer, setting the standard for engineering excellence and clean code., • DevOps Excellence: Managing our infrastructure via Pulumi to ensure the high-availability and security standards required by global research institutions. The Tech Stack: We believe in using the right tool for the job. You will manage the current foundation while evolving it: • Current Core: PHP 8 / Symfony / Doctrine API, React / TypeScript Frontend., • Cloud/Infra: AWS (Fargate, ECS, Lambda), Pulumi (IaC), MySQL., • The Frontier: This is your domain. You will lead our transition into Vector Search, Hybrid Search Engines, and AI Orchestration. Who You Are: • A Technical Owner: You’ve scaled production web apps and are comfortable across the full stack and infrastructure., • Pragmatic AI Enthusiast: You don't need a background in AI, but you are excited to build production-ready AI features (RAG, Agents) that solve real problems., • Empathetic Mentor: You enjoy leveling up junior talent and collaborating deeply with product peers., • Mission-Driven: You want your work to help scientists cure diseases and solve global challenges. Skills Required: • 5+ years of leading development teams, • 5+ years of leading architect, • 5+ Years of AWS DevOps experience, • Experience coding with the following languages/technical solutions - PHP 8 / Symfony / Doctrine API, React / TypeScript Frontend Why Labstep & STARLIMS? • Impact: Your code directly supports the world’s leading scientists and researchers., • Stability & Perks: Enjoy the comprehensive benefits package of a large corporation—including private healthcare, pension, and enhanced job security—without the corporate red tape., • The "Startup" Feel: We remain a small, agile team that moves fast, experiments often, and values your voice., • Work-Life Balance: Remote-first flexibility with meaningful monthly in-person collaboration in London. STARLIMS is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Senior Contracts Manager - International markets Ready to make your application Please do read through the description at least once before clicking on Apply. Location Chester, North West England (Hybrid: 23 days per week in-office). Languages Fluent English is essential. Fluent also in either Spanish, Italian, Portuguese, French, Mandarin, or German is preferred but not essential The Company Our client is a highly successful global organisation experiencing rapid growth across global markets. To support this expansion, they are seeking a Senior Manager to join their international enterprise contract facilitation team. The Role of the International Senior Contracts Manager As Senior Manager you will manage the delivery of a contracting capability across international markets (EMEA, APAC, and Canada). Typically this will cover supporting contract review, issue identification, negotiation and escalation management in collaboration with the contract legal support team and other cross-functional stakeholders. Key Responsibilities: • Lead and support the training and development of international Contract Facilitators, • Collaborate with the International Director to drive team performance, accountability, and continuous improvement., • Manage multiple complex contract projects across international markets., • Resolve complex negotiation issues and drive deals to execution., • Ensure compliance with legal standards and escalation protocols., • Act as the final escalation point for contract-related queries in the Director's absence., • Facilitate highly complex international contracts, including drafting, redlining, and negotiation., • Communicate contractual terms and risks clearly to internal stakeholders., • Develop and maintain training materials focused on negotiation and SOPs., • Collaborate with CLS and International Legal to keep templates and playbooks current., • Analyze and report on SLAs, KPIs, and performance metrics to support strategic planning., • Recommend and implement process improvements, automation, and standardization, • Fluent English is essential. Fluent also in either Spanish, Italian, Portuguese, French, Mandarin, or German is preferred but not essential, • Formal legal education (LLB, paralegal certification, etc.) is mandatory, • Proven experience in contract redlining and negotiation., • Leadership experience in legal or contracting roles within Pharma/Biotech/CRO., • Leadership & Team Development skills, • Expertise in international contracting, including regional nuances (EMEA/APAC/Canada), • Excellent understanding of pharma contracting compliance and policies., • Experience with Contract Lifecycle Management (CLM) tools; familiarity with Icertis, preferred. xrnqpay, • Demonstrated ability to manage intake, template selection, drafting, negotiation, and execution, • Excellent communication and stakeholder engagement skills

Regulatory Affairs Manager (EU) | Leading Pharma We’re hiring a Regulatory Affairs Manager to support products in development and post-MAA, contributing to EU regional clinical regulatory strategy and supporting EU Regulatory Leads across global development and lifecycle activities within a leading pharmaceutical organisation. What you’ll do • Lead and support planning, coordination, and preparation of EU regulatory submissions, • Contribute to EU clinical regulatory strategy and risk assessment/mitigation, • Provide regulatory guidance across R&D and product lifecycle activities, • Support and participate in EU Health Authority interactions and meeting preparation, • Help ensure post-approval compliance and inspection readiness What we’re looking for • 5+ years’ pharma/biotech experience, including Regulatory Affairs experience, • EU regulatory submission experience (clinical and/or lifecycle), • Strong understanding of EU regulations, guidelines, and submission processes, • Excellent communication, organisation, and stakeholder management skills, • Life/Health Sciences degree (preferred) About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

A global biopharmaceutical company is offering an Engineering Internship located in Liverpool, providing students hands-on experience in pharmaceutical manufacturing. Interns will collaborate with seasoned professionals on critical engineering projects, gaining vital skills while contributing to vac

A leading recruitment firm in the UK is seeking a Mechanical Design Engineer. The role involves designing and improving process equipment and systems, alongside preparing technical specifications.

The role involves 12-hour shifts and requires candidates to possess strong adaptability and a focus on safety and quality.

A global medical products company in the UK is seeking a Territory Business Manager for Continence Care. This field-based role requires expertise in the medical/pharma industry, strong communication and selling skills, and ability to engage with clinical stakeholders. Key responsibilities include dr

Are you an experienced warehouse professional looking to take the next step in a highly regulated, fast-paced environment? Join a world-renowned pharmaceutical organisation where your work directly supports the delivery of life-changing clinical materials across the globe. This is more than a warehouse role, you'll be a key part of a specialist team ensuring vital materials are received, handled, stored, and distributed safely and efficiently in line with production and shipping timelines. What You'll Be Doing Overseeing the receipt, sampling, storage, picking, and dispatch of clinical trial materials Operating within both warehouse and dispensary environments, maintaining the highest standards of accuracy and compliance Carrying out materials and warehouse transactions using SAP systems Ensuring all activities align with GxP, EHS, and internal procedures Supporting audits and inspections while maintaining strict adherence to transport security, COSHH, and hazardous goods regulations Working closely with Quality teams to maintain approvals and full chain of custody Safely operating reach and counterbalance forklift trucks What We're Looking For Proven background in warehouse, logistics, or materials management (ideally within pharma or another regulated industry) Good understanding of GxP principles (preferred) Valid RTITB (or equivalent) licences for reach and counterbalance forklifts Experience handling or transporting hazardous goods Strong IT skills, including SAP and Microsoft Office A proactive, flexible approach with excellent communication skills and a strong team mindset Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role

Talentmark are recruiting for a Warehouse Operator to join a global pharmaceutical company on a contract basis for 12 months. Salary: £15.38 per hour PAYE (35 hours per week) Warehouse Operator Role: Manage goods receipt, sampling, storage, dispensing, and dispatch of clinical trial materials within warehouse and dispensary environments. Support UK depot and materials management activities in line with production schedules and shipping timelines. Carry out warehouse, materials management, and distribution transactions using SAP systems. Ensure all operations are conducted in accordance with GxP, EHS regulations, and standard operating procedures. Maintain compliance with transport security procedures, COSHH regulations, and hazardous goods legislation.Your Background: Proven experience in materials management or logistics, ideally within a pharmaceutical or regulated environment. Working knowledge of GxP guidelines. Valid RTITB qualification for Reach and Counterbalance forklift trucks. Experience handling and transporting hazardous goods. Strong IT skills, including SAP and Microsoft Office applications.Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Location: This role is based at our client’s site in Moreton, Essex. Apply: For more information, or to apply for this Warehouse Operator please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

Talentmark are recruiting for a Packaging Technician to join a global pharmaceutical company on a contract basis for 12 months. This is a fully site-based role in Moreton, Wirral. Rate - Paying up to £15.66 per hour PAYE This is a shift-based role working on one of these two options: Option A : Mon-Thurs : 7am to 3pm (2 x 20min breaks and 1 x 30min lunch) Fri : 7am to 12pm (1 x 20min break) Option B : Mon-Thurs : 830am to 4.45pm (2 x 20min breaks and 1 x 30min lunch) Fri : 8.30am to 12.30pm (1 x 20min break) Salary: £15.66 ph PAYE Packaging Technician Role: Primary packaging (bottle filling) of oral dosage forms. Labelling and assembly of clinical trial supplies. Complete electronic batch documentation, equipment logbooks and other documentation. Start-up, execute, cleaning and completion of clinical trial packaging operation.Your Background: Experience of packaging and labelling environment in a GMP environment. Working knowledge of SAP. Basic knowledge of clinical trial operations would be advantageous. Good communication and teamwork skills.Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Apply: For more information, or to apply for this Packaging Technician please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

5 Month Contract working in the Filling team. 4 on 4 off shift pattern days and nights. Based in Speke in Liverpool. Working under the Team Leader, the Process Technician is responsible for executing the manufacturing processes in the Aseptic Filling department in accordance with written procedures. The role holder will provide (be trained in) the technical skill sets necessary to manufacture high quality vaccines in a compliant, efficient and cost-effective manner. Responsibilities Carries out all sterile filling process operations using local SOPs and batch documentation whilst in full compliance with cGMP to meet production schedule demands. To work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines and site procedures for Health, Safety and Environment. When manufacturing ensure that all Departmental SOPs and MIs are followed and: • Ensure appropriate control, monitoring and delivery of activities in their area of work. * Ensure that all documentation is completed correctly, accurately in a timely manner and signed by the relevant personnel. * Carry out final documentation review and sign off to ensure documentation is right first time. * Ensure compliance to Health and Safety regulations. Consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues. To actively maintain and promote a cGMP compliant culture, ensure that the highest standards of housekeeping and safety are applied within the area in accordance with the Orange Guide and CFR regulations and to apply the principles of Lean Manufacturing, Problem Solving, 5S ,Waste Elimination and Energy Efficient Activities in support of Continuous Improvement. To maximise their individual contribution so that team objectives are achieved. To work as a team member, providing and receiving feedback to team members and their team leader. To communicate and liaise with members of other teams in order to meet the business's objectives. When required, to flexibly support other departments - providing adequate training is received and it is safe to do so. Attend all compulsory and allocated training courses required for the role. Ensure that all training is completed in a timely manner and that personal training records are kept up to date. To continue to develop new skills, competencies and behaviours to fulfil both current and future business needs. The role holder will be able to demonstrate the application of the skills required for their role. To contribute ideas and action in order to improve team, process and equipment performance. To support process improvement and uphold Seqirus Values and Behaviours. Support organisation change and process improvements. Aseptic Filling - Specific Tasks Include: • Movement of materials using pallet trucks (manual and electric) to ensure manufacturing operations are efficient and production demands are met. * Cleaning and disinfection of production rooms and equipment to maintain cleanroom, cGMP and HSE standards. * Cleaning, preparation, sterilisation, assembly and disassembly of production equipment * Performance of In Process Control checks and Environmental Monitoring to ensure the isolator environment is maintained and products are made within specification. * Operation of the Filling production line including use of machine interfaces, performing VHP/CIP/SIP cycles, monitoring the batch and performing interventions Knowledge, Skills & Competencies Filling of sterile products / Aseptically qualified (e.g. sterile connections, sterility assurance) / Use of Isolator technology. Attention to detail and high personal concern for standards, integrity, communication, and discretion. Proven knowledge of cGMP. Basic mechanical aptitude or knowledge of electronic/mechanical equipment Competent in using multiple computer systems e.g. PCS, GLIMS, SAP and production line machine interfaces Education Requirements Relevant degree qualification preferred Experience Requirements 1+ years' experience and competence in cGMP and sterile product production operations in the Biotech or Pharma industry preferred Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser

Talentmark is recruiting for a Clinical Supply Chain Logistics manager to join a global pharmaceutical company on a contract basis for 12 months. Salary: Paying up to £34 per hour PAYE Clinical Supply Chain logistics manager: Provide day-to-day operational oversight of all logistics activities for assigned clinical supply programs, ensuring delivery of IMP. Act as the single point of contact (SPOC) for logistics-related activities for designated studies, working with Study Teams, Regional Delivery Leads (RDLs), Trial Supply Managers (TSMs), and external partners. Provide weekly status reporting, including STO health, shipment execution, risks, mitigations, and prioritization.Your Background: Bachelor’s degree (or equivalent) in Supply Chain, Life Sciences, Engineering, or a related field. Proven experience in clinical supply chain logistics operations, preferably in a global clinical trial environment. Strong hands-on experience with STO management, shipment execution, and issue resolution. Demonstrated ability to operate effectively in high-pressure, time-critical (hyper-care) environments. Excellent communication skills with the ability to interface across study teams, regions, and external partners. Strong organizational skills, attention to detail, and ability to manage multiple priorities simultaneously. Experience working with external partners (e.g., CMOs, depots, logistics providers) is strongly preferred.Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. Location: This role is based at our clients site in Moreton, Wirral, and allows for hybrid working (50/50 split). Apply: For more information, or to apply for this Clinical Supply chain logistics manager please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only). It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check