Controls Engineer Hybrid 6 Month Contract Day Rate up to £600 a day Inside IR35 Commissioning Engineer main skills: • Advanced technical expertise in industrial automation systems (TIA Portal 16+, Codesys 3.5, HMI, VFDs, Profinet, IO-Link) • Proficiency in programming and configuring with TIA Portal 16+ • Proficiency in Codesys 3.5 (preferred) • Strong problem-solving and troubleshooting abilities for complex systems • Hands-on experience with camera systems and Linux OS (preferred)
Commissioning of the controls systems of a new automation line. Troubleshoot issues with the direct support of (remote) software experts. Interact with the electrical and mechanical installation vendors and other site stakeholders to ensure a smooth overall commissioning. Provide a short daily report on progress.
Commissioning Engineer main skills: • Advanced technical expertise in industrial automation systems (TIA Portal 16+, Codesys 3.5, HMI, VFDs, Profinet, IO-Link) • Proficiency in programming and configuring with TIA Portal 16+ • Proficiency in Codesys 3.5 (preferred) • Strong problem-solving and troubleshooting abilities for complex systems • Hands-on experience with camera systems and Linux OS (preferred)
Logistics’ future automation will run with in-house controls, essentially our own software and controls systems. In 2025, “ADTA” automation lines will be launched with In-House Controls. Commissioning engineers are required to complete the ADTA commissioning procedure, ensuring schedule and quality.
I am looking to speak with Quality & Compliance Managers looking for their next contract opportunity with a Global Pharmaceutical Manufacturing organisation based out of Sandwich, Kent. This position reports to the Regulatory Quality Oversight Lead for Submission Process & Compliance Excellence, Submissions Management and works with GRS BU Regulatory Strategy (above country and in country), Global CMC, Regulatory Operations, Safety and Regulatory Quality, Information Management, COE SOP & Training, appropriate governance and advisory bodies and external vendors if applicable. Position Purpose The Quality Oversight and Compliance Manager will be responsible for driving improvements to existing processes, supporting implementation and monitoring of initiatives related to pan-regulatory (e.g. Manufacturing, Regulatory Strategy, CMC, Submissions, Translation) information and processes globally through data reporting/ metrics analysis. The Quality Oversight and Compliance Manager works with global delivery teams to improve the quality and compliance associated with regulatory processes and product/license information. Primary Responsibilities Identifies opportunities for improvement of pan-regulatory data and business processes and procedures, through the collection and analysis of metric data in collaboration with Information Management, Analytics + Reporting, business process owners and other stakeholders. Provides accurate and detailed reports and presentations on the above activities for senior management, Quality councils and governance committees as required including executive summaries to Senior Management. Identifies procedural/compliance gaps associated with in scope processes and establishes mitigation and remediation plans with business process owners that provide optimal balance of compliance and business need. Provides support to stakeholders in ensuring inspection readiness, preparing for audits/ inspections and provide remediation support for audit (or inspection) findings. Participates on cross functional teams to execute quality improvements. Leads/provides input to the investigation of suspected Quality Events (QEs), Corrective / Preventative Action (CAPA) plans and audits/inspections and owns resulting actions as appropriate. Generates metrics and data analysis in support of Quality Plans and other compliance initiatives Technical Skill Requirements Experience in leading investigations and managing CAPA plans Strong knowledge of the drug development process, Regulatory Affairs, Regulatory Strategy and Submissions Management. Proven fluency with use of soft skills and ability to adapt core project management skills successfully within a dynamic line environment. Understanding of systems and electronic technologies used to support regulatory and submission process and planning activities and experience in process development and new technology implementation. Translates data into information to support the business in taking action and decision making Ability to transform ambiguous situations/discussions into structured outcomes Management of change in partnership with key stakeholders Ability to lead and operate seamlessly to influence colleagues across the organization and ensure delivery to time and quality driving highly complex projects to meet evolving business needs. Proven aptitude in project management If this is something you'd be interested in, send your CV to
Commissioning Engineer Remote 6 Month Contract Day Rate up to £600 a day Inside IR35 Commissioning Engineer main skills: • Advanced technical expertise in industrial automation systems (TIA Portal 16+, Codesys 3.5, HMI, VFDs, Profinet, IO-Link) • Proficiency in programming and configuring with TIA Portal 16+ • Proficiency in Codesys 3.5 (preferred) • Strong problem-solving and troubleshooting abilities for complex systems • Hands-on experience with camera systems and Linux OS (preferred)
Commissioning of the controls systems of a new automation line. Troubleshoot issues with the direct support of (remote) software experts. Interact with the electrical and mechanical installation vendors and other site stakeholders to ensure a smooth overall commissioning. Provide a short daily report on progress.
Commissioning Engineer main skills: • Advanced technical expertise in industrial automation systems (TIA Portal 16+, Codesys 3.5, HMI, VFDs, Profinet, IO-Link) • Proficiency in programming and configuring with TIA Portal 16+ • Proficiency in Codesys 3.5 (preferred) • Strong problem-solving and troubleshooting abilities for complex systems • Hands-on experience with camera systems and Linux OS (preferred)
Logistics’ future automation will run with in-house controls, essentially our own software and controls systems. In 2025, “ADTA” automation lines will be launched with In-House Controls. Commissioning engineers are required to complete the ADTA commissioning procedure, ensuring schedule and quality.
If you are interested please apply or send your CV to
Community Engagement and Communications Specialist Contract length: 6 months High Wycombe office hybrid working Pay: Up to £400 a day Key job responsibilities Key Responsibilities: • Develop and implement a comprehensive community engagement strategy to foster a vibrant and active user community within the Adobe Program that can advocate within the wider community of marketers. • Create and deliver compelling communication materials, including newsletters, social media posts, and internal updates, to keep the community and the wider Marketer community informed and engaged. • Lead EU training and support of assigned markets and flex to cover other regions/time zones and markets as demand requires • Plan and execute community events, both online and offline, to encourage participation and strengthen community bonds. • Collaborate with cross-functional teams, including marketing, Digital, Marketing Technology and Commercial Operations, to align community engagement efforts with overall business goals.
This individual will play a crucial role in building and nurturing our community, activating users, and ensuring effective communication across various channels within the Adobe Program. The ideal candidate will have a strong background in communications, community management, and user engagement, with a focus on leveraging technology to enhance marketer processes and train them on both tools and processes. Key Responsibilities: • Develop and implement a comprehensive community engagement strategy to foster a vibrant and active user community within the Adobe Program that can advocate within the wider community of marketers. • Create and deliver compelling communication materials, including newsletters, social media posts, and internal updates, to keep the community and the wider Marketer community informed and engaged. • Lead EU training and support of assigned markets and flex to cover other regions/time zones and markets as demand requires • Plan and execute community events, both online and offline, to encourage participation and strengthen community bonds. • Collaborate with cross-functional teams, including marketing, Digital, Marketing Technology and Commercial Operations, to align community engagement efforts with overall business goals. • Monitor and analyze community feedback and engagement metrics to continuously improve processes and Adobe platform. • Serve as the primary point of contact for community members, addressing their questions, concerns, and feedback in a timely and professional manner. • Identify and nurture community champions and influencers to amplify our message and drive user activation. • Stay up-to-date with industry trends and best practices in community management and communications to ensure our strategies remain innovative and effective. • Utilize Adobe tools to streamline content operations and enhance user experience within the Content at Scale Team.
Qualifications: • Bachelor's degree in Communications, Marketing, Public Relations, or a related field. • Proven experience in community management, communications, or a similar role. • Excellent written and verbal communication skills, with the ability to craft engaging and persuasive content. • Strong interpersonal skills and the ability to build and maintain relationships with diverse stakeholders. • Proficiency in using Adobe tools, social media platforms, content management systems, and analytics tools. • Creative thinker with a passion for community building and user engagement. • Ability to work independently and as part of a team in a fast-paced, dynamic environment. • Strong organizational skills and attention to detail.
If you are interested please apply or send your CV to
SAP FPSL Functional Consultant - Consultant Hybrid - London Pay is up to £600 a day Inside IR35 9 Month contract Experienced SAP FPSL Functional Consultant to support the implementation of SAP Financial Products Subledger (FPSL) in a complex multi-core-source system landscape. The role will focus on IFRS 9 accounting rules, event-based accounting models, and financial integration within a banking/financial services environment. The consultant will work closely with Finance, Accounting, and IT teams to develop and optimize the FPSL framework, ensuring compliance with regulatory and business requirements
The consultant will work closely with Finance, Accounting, and IT teams to develop and optimize the FPSL framework, ensuring compliance with regulatory and business requirements. Key Responsibilities Lead the design, configuration, and deployment of SAP FPSL with a focus on IFRS 9 accounting rules. Define and implement event-based accounting models, posting logic, and subledger-to-general-ledger mappings. Collaborate with business stakeholders to develop accounting rules frameworks, valuation models, and financial product mappings. Ensure seamless data integration from multiple core banking and general systems into FPSL. Work with testing teams to develop UAT and system validation strategies.
Skills & Experience Required 3+ years of experience in SAP FPSL accounting solutions for banking ( preferred) Deep understanding of IFRS 9, financial instruments, subledger accounting, and risk-based reporting. Experience integrating SAP FPSL with multiple core source systems. Strong knowledge of ledger setup, account determination, and financial reporting structures. Experience in multi-entity, multi-ledger, and multi-GAAP reporting environments. Familiarity with treasury and risk management principles Certifications - SAP FPSL or earlier versions ( SAP Bank Analyser , Smart AFI etc) is a plus.
If you are interested please apply or send your CV to
Senior Software Engineer 12 Month Contract Location – Wrexham - Hybrid Salary 40/50k Inside IR35
As a Senior Software Engineer, you will:
Be a hands-on technologist spending a lot of your time in code across all parts of the Atom5 platform Work in an agile manner, develop features as per sprint priority plan Work as part of the team, sharing and reviewing ideas, mentoring and guiding team members through technology architecture and implementation details Keep up to date with the evolving industry, embracing new languages and frameworks, containers and cloud, and not be afraid to dig deep and learn new things all the time Have an inquisitive and curious mind, often exploring the inner workings of the tools and libraries you use to understand how they work
The key skills and qualities of a Senior Software Engineer:
Demonstrable understanding of best practices in software engineering Good communication skills demonstrating the process and progress to stakeholders, as well as internal team communication Proficiency in at least one general purpose programming language (Java or Javascript/Typescript) with willingness to learn new languages and technologies Experience or familiarity with some of the core platform frameworks and libraries: Spring Boot, ReactJS, ReactNative, Docker Familiarity with Linux environment Enjoy participating in the full lifecycle of the software product: from idea and design, via implementation, to operational considerations Be able to write clean code, take pride in your work and value simplicity, testing and productivity as part of your daily routine, always putting user experience and security first
If you are interested please apply or send your CV to
We are working with a Croydon based Medical Equipment Manufacturing organisation committed to innovation and excellence in their search for an experienced QA Validation Specialist.
This role would suit a Quality Assurance professional with a background in Medical Devices and Validation activities looking for a new permanent position with plenty of progression opportunities.
The Role: Validation activities and ensuring compliance with EU GMP and regulatory requirements. Management and improvement of the Quality System including supporting improvement activities through CAPA Conducting Internal Audits and Quality Inspections on finished products Training of employees in Quality Systems, Tools and Objectives Conducting Audits on manufacturers and suppliers
About you : Has previous experience in medical device or pharmaceutical manufacturing. Possesses practical experience in manufacturing technology and quality assurance. Understands Quality Management Systems for medical devices (EN ISO 13485, 21 CFR 820). Experienced in validation/qualification and project work/project management.
If you are interested and want to learn more, apply with the link or send me a message
Job Title: Quality Validation Specialist Job Type: Full Time, Permanent Position. Location: Great London/ Hertfordshire area, UK. (On site) Remuneration: Competitive salary and package.
Cpl Life Sciences is partnering with a growing pharmaceutical company that specialise in Oncology and Neurology. Due to growth within the business, they are looking for a Quality Validation Specialist to join the Quality Operations team.
This role you will be responsible for ensuring that electronic systems within the Quality Control Laboratory and the Quality Systems operate in accordance with the requirements of the departmental Standard Operating Procedures.
Role Responsibilities: Ensure EML’s Electronic TrackWise Quality Management System (QMS) and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and Corporate expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required. Support the maintenance and administration of EML’s Electronic TrackWise Quality Management System (QMS) to maintain an effective QMS to meet EML’s requirements. Support the effective management of the administration of QC laboratory system applications providing independence of access for administrator activities. Ensure Qualification and Validation of EML equipment, processes, systems is/are performed in line with EML procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of EML procedures supporting Qualification and Validation ensuring they are current with updated requirements for Qualification and Validation and cGMP, cGxP expectations. To act as a Quality Subject Matter Expert in relation to ensure compliance of Qualification, Validation and all CSV activities within EML control.
Requirements/Qualifications: Ability to understand and analyse user requirements to facilitate changes and system improvements. Proficient knowledge of electronic systems, CSV and GAMP requirements. Good understanding of the requirements of data integrity and application to system management. Good understanding of Quality Control Systems and analytical software and electronic Quality Systems. Ability to interpret complex data and present key findings. Ability to describe technical information in easy-to-understand terms. Good understanding of GMP Guidelines and Regulations. Knowledge of the qualification and validation requirements for equipment and electronic systems. Maintain knowledge and understanding of technical advancements in electronic systems.
For more information, please forward your up-to-date CV to Please ensure you hold the full right to work in the UK.
Content Adaptation Manager- German speaking Contract length: 6 months Remote Pay: Up to £500 day Key job responsibilities Must be fluent in German • Marketing and content savvy combined with strong Project Management skills to be able to manage multiple workflows at the same time • Experience with content adaptation work either in creative agency or on a customer side • Solid understanding of content quality aspects to be able to drive Agency deliverables on time and with the right quality • Experience with working with DAM/MLR tools
POSITION PURPOSE:
The CE&E IMI team aims to design and deliver intentional, impactful customer experiences for HCPs and patients through integrated engagements and solutions. This role is part of the Customer Experience, Content & Partnerships Excellence team of the CE&E, IMI organization - a team of innovative, passionate talent focused on designing and deploying personalized and outcome-oriented customer experiences grounded in deep insights and human-centered design.
The Content Adaptation Manager role will work closely with Agency of choice to deliver quality creative adaptations of centrally created content (driven by CX Strategy& Design team) based on a clear input coming from CX Engagement & Channels team members who will work with countries on Engagement Plan per brand.
The Content Adaptation Manager will be also in charge of a process on the line between CX Engagement & Channel Team and Content Hub Production team, making sure the briefs are received, uploaded to Fuse and managed with clear understanding on the localization ask.
MAJOR ACCOUNTABILITIES: •Work with Cx Engagement & Activation Director and Agency to understand a customer journey and content plan to work with Agency on creative adaptation of centrally delivered assets – this can mean existing content adaptation or/and creation of channel specific content from scratch based on Cx Strategy & Design Master Asset story. •Brief Content Hub Production Team on content production and manage the rounds of changes with Asset Owner •Support adaptation of above market content to local label requirements to ensure content is compliant and ready for execution in markets •Support content tracking management and demand forecasting and prioritization process with Content Hub to ensure timely executions •Work together with Content Hub and Cx Activation Director to agree on engagement plan delivery via localization
MINIMUM REQUIREMENTS: •Needs to be Fluent in German •Marketing and content savvy combined with strong Project Management skills to be able to manage multiple workflows at the same time •Experience with content adaptation work either in creative agency or on a customer side •Solid understanding of content quality aspects to be able to drive Agency deliverables on time and with the right quality •Experience with working with DAM/MLR tools
DESIRABLE REQUIREMENTS: •Firm understanding of the regulatory environment in marketing to HCPs •Demonstrated strong skills in oral and written communication, project management •Highly collaborative, ability to interact and partner with Agencies of choice
If you are interested please apply or send your CV to
Job Title: Quality Control Analyst Job Type: 1-year Fixed Term Contract Location: Hertfordshire, UK – Hybrid Remuneration: Competitive salary and package
An exciting opportunity to join a medium-sized pharmaceutical company on a 1-year fixed-term contract. As a QC Control Analyst, you will be responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times.
To ensure that operations conducted are performed in accordance with the requirements of Corporate Standards, Quality System, GMP and GDP Guidelines, and Industry Standards.
Responsibilities: To test all materials according to agreed specifications and procedures. To qualify (URS, IQ, OQ, PQ) all laboratory equipment. To maintain and calibrate all laboratory equipment according to approved procedures. To maintain all laboratory Quality Systems and Quality Management Systems in compliance according to approved procedures. To write under supervision, all SOPs associated with QC support. To support the internal and external audit process and audit schedules as appropriate. To support the preparation and hosting of competent authority inspections. To raise and support the investigation of deviations and associated CAPA’s. To support technology transfer projects and in particular any QC aspects of these. To support the implementation of change control activities. To support the process for data collection for PQR’s. To support the collection of data for reporting Quality Assurance Performance Indicators. To support the implementation and management of stability programmes To perform any other appropriate duties at the request of the QC Heads.
Requirements: A relevant life sciences degree with at least 1 year of prior QC experience. Ability to establish and maintain effective working relationships and communication links, affiliated organisations and other customers. Extensive knowledge of Quality Control, Quality Assurance, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical products. Good technical and scientific judgement. Ability to interpret complex data and present key findings. Demonstrated Knowledge, understanding and application of GMP Guidelines and Regulations. For more information, please contact The role does not offer sponsorship and you must be in a communicable distance to Hertfordshire.
