Trabajos eu en CoventryCrear alertas

Company Description VerIQ Limited is a UK-based MedTech clinical trial accelerator enabling faster, high-quality clinical research for medical device innovators. Through a coordinated network of pre-qualified trial sites, research nurses, and clinical investigators, we deliver rapid study start-up, accelerated recruitment, and reliable data quality. Led by a highly experienced team in complex clinical investigations, we partner with organisations ranging from early-stage innovators to global multinationals to design and execute efficient, regulator-ready studies. Our capabilities extend beyond trial delivery to include clinical strategy, regulatory pathways (FDA, UKCA, CE), health economics, and market access planning—supporting the safe, effective, and timely translation of innovative technologies into patient care. Salary: £40,000-50,000 + bonus + benefits Role Description As a Clinical Project Manager, you will play a leadership role within our growing organisation. You will be supporting the Senior project manager with planning, managing, and completing clinical investigations for emerging and innovative medical technologies, while providing strategic consultation on study design, regulatory approach, and commercialisation strategy. We anticipate the post will involve hybrid working, with the successful candidate working part of the week from office facilities in Coventry/Warwickshire. We welcome applicants from industry, NHS R&D, NIHR/UKRI-funded research infrastructure, Academic Clinical Trials Units (CTUs), clinical research networks, and university-based clinical research offices, as many of the competencies required for this role are directly transferable to a CRO environment. Strong operational leadership, regulatory familiarity, and experience managing complex, multi-stakeholder clinical research programmes are particularly valued. This role requires operational excellence, autonomy, and strong client-facing and organisational leadership skills within a patient care focused environment. We anticipate the post will involve hybrid working, with the successful candidate working part of the week from office facilities in Leamington Spa/Warwickshire. We welcome applicants from industry, NHS R&D, NIHR/UKRI-funded research infrastructure, Academic Clinical Trials Units (CTUs), clinical research networks, and university-based clinical research offices, as many of the competencies required for this role are directly transferable to a CRO environment. Strong operational leadership, regulatory familiarity, and experience managing complex, multi-stakeholder clinical research programmes are particularly valued. This role requires operational excellence, autonomy, and strong client-facing and organisational leadership skills within a patient care focused environment. Responsibilities • Drive the full lifecycle management of medical device clinical trials, ensuring delivery to scope, timelines, quality standards, and budget., • Develop and maintain project plans, risk assessments, monitoring strategies, and all operational project documentation., • Maintain oversight with sponsors, regulatory authorities, clinical investigators, CRO partners, and internal teams., • Review and approve study related documents (proposals, protocols, amendments, plans, reports and CSR’s)., • Provide expert input on clinical development strategy, regulatory pathways (FDA, UK MDR, EU MDR), and market access planning for UK and EU markets., • Oversee site feasibility, site selection, and investigator engagement to ensure optimal site performance and protocol adherence., • Assist with the preparation and contribution to regulatory and ethics submissions, including CI/IRAS documentation, Clinical Investigation Plans, and Device Dossiers., • Manage budgets, vendor contracts, and outsourced activities including monitoring, data management, and safety functions., • Ensure compliance with applicable UK and international regulations including GCP, ISO 14155, and company standard operating procedures (SOPs) across all study phases., • Support continuous improvement initiatives and contribute to the development of scalable processes and SOPs and training., • Prepare and present clear project updates, metrics, and governance materials for internal and external stakeholders., • Promote a compliance culture advocating the adherence to the highest standards and ethical integrity, always ensuring human subject protection and reliability of trial results., • Conduct or coordinate local investigator meetings as needed and ensures relevant training documentation is archived in the trial master file., • Identify risks, manage escalations, and implement mitigation strategies. Requirements • Significant experience (typically 5+ years) in clinical project management within a CRO, medical device company, or healthcare research organisation., • Broad protocol knowledge; therapeutic knowledge desired., • Demonstrated expertise in managing complex multi-centre clinical investigations, ideally under ISO 14155, ICH-GCP and EU MDR/UK MDR frameworks., • Excellence in leadership and communication with demonstrable experience of line managing individuals and teams to successful outcomes., • Strong understanding of UK and EU regulatory and ethics processes, including IRAS/HRA submissions and MHRA device investigation pathways., • Experience providing strategic direction on clinical development, regulatory strategy, and market access/commercialisation planning., • Track record of managing multiple concurrent projects efficiently and effectively to achieve successful outcomes., • Strong vendor oversight and financial management capabilities, including budget development and contract negotiation., • Excellent communication, presentation, and client-facing skills, with the ability to convey complex information clearly., • Ability to work in complex teams with a range of expertise to achieve shared goals., • Ability to thrive in a fast-paced start-up culture with evolving operational processes., • Ability to support database design and develop and lead data management plans that align with UK and international regulation and provide high quality data for clinical investigations., • Organisation- Planning, time management and prioritization skills. Ability to organize resources needed to accomplish task, set objectives and provide clear direction to others, experience planning activities in advance and taking into account of possible changing circumstances., • Ability to use a wide range of IT systems including common Microsoft applications, video calling facilities and other technologies relevant to the business., • Bachelor’s degree in a life science or related field (advanced degree preferred but not essential)., • Willingness to travel within the UK and internationally as required – 20-30%, • Applicants must have the right to work in the UK. Equal opportunities VerIQ Limited is an equal opportunities employer committed to creating an inclusive working environment for all employees. We value diversity and welcome applications from candidates of all backgrounds, experiences, and identities. Employment decisions are made based on merit, capability, and business need, without regard to age, disability, gender identity or expression, marital or civil partner status, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. We are dedicated to ensuring that every individual is treated with fairness, dignity, and respect throughout the recruitment process and their employment with the company. Apply Please submit your CV to contact info@veriq.co.uk quoting reference CPM-002.

Position Title: Prototype Parts Analyst Duration: 9 Month Contract Location: Whitley Applicants MUST have proof of immediate, on-going and valid eligibility to work full time in the UK and travel within the EU. The Opportunity: The PVO team, in which the Engineering Parts Logistics team are based, are a critical area within Product Engineering (PE) with an important role in the creation of prototype vehicles. Working under the Product Engineering Operations (PEO) function, we are directly responsible for all the Clients' prototype vehicle build Preparation. Often seen as a key interface between Vehicle Programme, Vehicle Engineering & Manufacturing teams, PVO work to create a strategy for successful prototype builds and we are currently in an exciting period whilst the Client expand their product portfolio. The main purpose of this role will be to support pre-production builds by obtaining and maintaining delivery promises from external supplier. Ensuring delivery promises meet build requirements / escalating issues. Parts are owned from dispatch to receipt in the Clients' storage locations and building supplier relationships is an integral part of the role while ensuring all NRP (Non Released Parts) are delivered on time. Knowledge, Skills and Experience: Essential: Previous experience of managing a portfolio of suppliers supporting production schedules Experience of managing prototype suppliers during pre-...

Ecommerce Assistant Location: Coventry Working Pattern: Monday–Friday, 37 hours (On-site) A growing international housewares business is looking for an Ecommerce Assistant to manage and develop its UK marketplace presence.. This is a hands-on role with ownership of day-to-day ecommerce operations and performance. Key Responsibilities • Manage daily operations across platforms, • Create, optimise and maintain product listings (SEO, content, images, A+ content), • Monitor inventory levels, coordinate replenishment and manage FBA/FBM fulfilment, • Plan and optimise marketplace advertising and promotions, • Handle customer enquiries, reviews, returns and escalations, • Analyse sales and performance data, preparing regular reports, • Ensure compliance with marketplace policies and UK/EU regulations About You • Strong Excel/Google Sheets and analytical skills, • Confident in SEO, PPC and writing effective product copy, • Highly organised, detail-focused and proactive, • Strong communication and problem-solving skills What’s on Offer • Excellent salary package, • 25 days annual leave, • Permanent, full-time role, • Opportunity to grow and shape a key ecommerce channel Candidates m...

VerIQ Ltd seeks a Clinical Project Manager to lead clinical investigations for medical devices. This role involves managing multi-stakeholder projects, ensuring compliance with UK and EU regulations, and contributes to the strategic direction of clinical development. Candidates should have significa

A leading automotive technology firm in Coventry is seeking an Advanced Manufacturing Engineering – IDEA Manager to oversee the execution of automation projects across EU & Africa.

Turbo Driving Recruitment Limited is looking for a skilled HGV Class 1 driver based in Coventry, West Midlands, UK. As an HGV Class driver, you will support their yearly EU contract, requiring you to have a minimum of 1 year’s experience with no major endorsements. Experience driving in the EU is

Advanced Manufacturing Engineering – IDEA Manager – Execution. The AME IDEA Manager – Execution supports the delivery of regional automation projects across EU & Africa JIT, Trim, and Structures plants, ensuring execution aligns with Lear's AME Roadmap. Lead cross‑functional team consisting

Turbo Driving are looking for HGV class drivers to support their yearly EU contract. Turbo Driving Recruitment Limited is hiring a. Experience of driving in the EU would be advantageous.

Parent and Child Foster Carer Do you have a spare bedroom in your home and a genuine desire to make a difference for a parent and their young baby or toddler? At Rees Fostering, we are looking for caring, patient and resilient people to provide a safe and nurturing home environment for parents who need extra guidance and support to build their confidence and parenting skills. If you have experience working with families perhaps as a midwife, maternity nurse, nursery worker, or in a community or support role this could be an opportunity to use your skills in a new and rewarding way. About the Role As a Parent and Child Foster Carer, youll welcome a parent and their baby or toddler into your home for a period of approximately 12 weeks. Youll work alongside our dedicated team of social workers and professionals to support the parent to develop their parenting capacity in a calm, safe and encouraging environment. Youll play a vital role in helping a family stay together and thrive using respect, empathy, empowerment and support to help build independence and confidence. Location: Birmingham, Coventry, Dudley, Herefordshire, Sandwell, Shropshire, Solihull, Staffordshire, Stoke-on-Trent, Telford and Wrekin, Walsall, Warwickshire, Wolverhampton and Worcestershire Benefits Refer a friend scheme Store discount Work from home Company events 24/7 support Essential Requirements A spare bedroom that provides enough space for a parent and their child, including room for a single bed, cot or Moses basket, wardrobe and chest of drawers. Time and flexibility to care for a parent and their child full-time A genuine interest in supporting families, while respecting and valuing them as individuals Ability to take parent and child to appointments and attend meetings/training as required Good spoken English and basic IT skills (or willingness to learn) Aged 21 or over British Citizenship, Indefinite Leave to Remain, or EU Settled Status (Student, Post-Study or Work Visas are not eligible) Desirable Good written English and record-keeping skills Access to a computer or tablet Able to drive, or willing to learn (depending on local transport links) At home full time or with flexibility in other commitments Experience No prior fostering experience is necessary as full training and support are provided. Previous experience of parenting, childminding, fostering, or working with children, families or vulnerable adults is beneficial, but not essential. If you have the right values and motivation, wed love to hear from you. The assessment process usually takes around 46 months and includes free training, background checks, and references (including an enhanced DBS). Financial Package While foster carers are not salaried employees, you will receive a generous weekly allowance when you have a parent and child placed with you. This covers the costs of caring for them and reflects your skills and commitment. Allowance: Earn between £800£1,300 per week, with generous tax relief available for foster carers. Additional payments: Start Up Grant up to £1000, Refer a friend scheme, Holiday allowance What We Offer Comprehensive training (initial and ongoing) Regular supervision and 24/7 support A dedicated supervising social worker Peer support groups and events for fostering households Membership of FosterTalk, including access to advice, discounts and tax guidance Support specifically for parents including 24/7 access to a mental health professional, financial advice, training and much more! Interested? If youd like to learn more about joining Rees Fostering as a Parent and Child Foster Carer, wed love to hear from you. Job Type: Full-time (home-based) Pay: Earn between £800£1,300 per week, with generous tax relief available for foster carers. TPBN1_UKTJ

SF Partners are supporting a brilliant Coventry based organisation that are looking to recruit a Material Planning Manager (returns) - Supply Chain & Logistics (UK Wide) Are you a data-driven supply chain professional with a passion for inventory optimisation and operational excellence? We're partnering with a growing logistics and distribution organisation to appoint a Material Planning Manager, responsible for managing forward and returns inventory across a multi-site UK network. This is a highly visible role, working closely with customers and operational teams to ensure stock is positioned correctly, service levels are maintained, and costs are controlled. The Role You'll take ownership of inventory planning and control across multiple sites, ensuring the right stock is in the right place at the right time. Key responsibilities include: Managing forward and returns inventory for customer-managed stock across a UK-wide network Translating demand forecasts and consumption data into actionable replenishment plans Defining planning parameters (safety stock, reorder points, min/max levels) Coordinating stock flow across sites to prevent shortages, excess, and capacity issues Monitoring inventory performance, including availability, ageing stock, and accuracy Driving inventory accuracy through robust controls, audits, and process improvements Acting as the key interface between customers, operations, and transport partners Communicating risks, constraints, and performance insights to stakeholders Developing KPI reporting (OTIF, stock turns, days of cover, forecast adherence) Leveraging systems and data (WMS/ERP/BI tools) to optimise planning and decision-making What We're Looking For Proven experience in material planning, inventory management, or supply chain planning Background within warehousing, distribution, or 3PL environments Strong understanding of replenishment models and customer-managed inventory Experience managing stock across multiple sites and stakeholders Highly analytical, with the ability to turn data into clear actions Strong stakeholder management and communication skills Exposure to process improvement methodologies (Lean, Six Sigma, Kanban, etc.) Desirable: Experience with CMI/VMI models Familiarity with WMS/ERP systems (e.g. SAP) Knowledge of UK/EU logistics or customs processes Relevant professional qualifications (APICS, CILT, Lean/Six Sigma)

Contributing to donor coordination and alignment with EU external cooperation priorities. EU Global Gateway Coordination Expert. European Union’s Global Gateway.

Principal Machine Learning Scientist | ADMET/Structural Biology | Series A - Drug discovery Platform | Fully Remote, EU | Base Salary Up to £160,000K, plus early equity+benefits. Responsibilities for the Principal Machine Learning Scientist | ADMET/Structural Biology | Series A - Drug discovery Pla

Experience within Oncology and/or CNS therapeutic areas. Exposure to a wide variety of clients and projects, including collaboration with leading global pharmaceutical companies.

Mid/Senior Back End Developer, Golang | Social Media, Scale-Up, 18 Million Users | Salary Up to £85,000 + Benefits & Bonus (EU/UK Remote). They are extremely well known in multiple countries across the world, such as the UK, US, Pakistan, and all over Europe. Requirements for the Mid/Senior Back En

Strong familiarity with European power markets and/or European carbon markets (EUA/UKA). European power or carbon markets. You will be joining a successful, fast-growing and entrepreneurial team.

Mid & Senior Backend Engineer (Go) | Drug discovery Platform, AI | Fully Remote, EU /UK| Base Salary Up to £110,000, plus early equity, benefits. This is a high-autonomy role where you will own the technical design and lifecycle of production services used by some of the world’s largest pharmaceu

We are looking for a UK local qualified Solicitor to take full charge of legal compliance, IP protection and anti-counterfeiting enforcement across UK & EU markets, supporting our consumer electronics /overseas brand business. Manage UK/EU IP compliance, trademark/copyright/infringement legal assess

B in AUM, we are the European leader in single-stock ETPs. This is a unique opportunity to shape our growth in one of Europe’s most sophisticated investment markets, connecting with brokers, wealth managers, platforms, institutions, and retail investors alike. Play a key role in expanding a leadin

Sales Director – Northern Europe & APAC | UK-Based. Sales Director – Northern Europe & APAC. Europe and APAC, including regular trips to Australia.

I’m currently working in partnership with a leading international QSR business that is continuing to scale across the UK and European markets. Own and develop the international supply chain strategy across the UK and European markets.

Director, Regulatory Affairs EU. Blackfield Associates are exclusively supporting the opportunity for a Regulatory Affairs Director to lead and expand EU regulatory capability within a global CDMO environment, with a strong focus on large molecule drug substances and Biologic products. Provide matri

We are a global specialist engineering company that creates breakthrough solutions.We are curious and like to solve problems, partnering with our customers to solve the demands of today and prepare for the challenges of tomorrow.We embrace innovation and care about outcomes that are good for busines

Join a highly successful business and leading Life Science Consultancy, delivering high quality solutions to make their clients’ businesses safer, more quality focused, compliant and ultimately more sustainable and successful.Reporting to the Practice Leader you will play a crucial role in the con

We are a global specialist engineering company that creates breakthrough solutions.We are curious and like to solve problems, partnering with our customers to solve the demands of today and prepare for the challenges of tomorrow.Weembrace innovation and care about outcomes that are good for business

Eurofins is seeking a Vice President of Business Development Discovery Europe to lead the business development strategy and regional marketing alignment. This role involves managing the sales organization and developing key account strategies to achieve sales targets across various therapeutic areas

Direct message the job poster from KES EU. We’re hiring for a prestigious European SAP consultancy. Referrals increase your chances of interviewing at KES EU by 2x.

Experience working across multiple European markets is a plus. We are seeking an EU E-commerce Lead to join a high-performing Digital Sales team within a globally recognised tier-1 consumer brand. Lead and manage weekly trading reviews across multiple European markets.

Energy One Limited is looking for a Head of Delivery to take charge of the end-to-end delivery of their EU portfolio, valued at €3–5m.

We are a global specialist engineering company that creates breakthrough solutions.We are curious and like to solve problems, partnering with our customers to solve the demands of today and prepare for the challenges of tomorrow.We embrace innovation and care about outcomes that are good for busines

Minimum 7 years of professional experience in EU environmental, sustainability, or circular economy legislation. Ability to analyse legal implications for non‑EU partner countries. Strong understanding of EU Green Deal, sustainability, and product legislation.

A global talent specialist is seeking an experienced EU E-commerce Lead to drive data-driven commercial performance within a tier-1 consumer brand.

This role is open to candidates across Europe and can be based in any country where IMI has an established presence, working remotely.

This senior role involves overseeing logistics, stock control, and EU export compliance, ensuring operational efficiency.

This role isopen to candidates across Europeand can be based inany country where IMI has an established presence, working remotely.

This role is open to candidates across Europe and can be based in any country where IMI has an established presence, allowing remote work.

An international consultancy is seeking a Legal Expert specializing in EU sustainability and circular economy legislation.

Note: This range is provided by iO Associates - UK/EU.

Wenn du einen EU-Pass besitzt, bereit bist, für die Dauer der Sommersaison umzuziehen, und Englisch sowie eine der folgenden Sprachen sprichst – Dänisch, Niederländisch, Finnisch, Deutsch, Polnisch, Norwegisch oder Schwedisch – dann lies unbedingt weiter!. Du bist lernfreudig und neugierig,

EU passport, EU work visa, French residency permit, or Carte de Séjour). Competitive seasonal salary paid in Euros (all staff will be on a French contract for 2026). Due to Brexit implications, applicants must hold EU documentation (e.

TUI Hotel or Service Rep | EU Nationals | Work Abroad | S26.

Assist with the delivery of a clean and safe user environment within various premises across East Ayrshire in order to assist with the promotion, delivery and integration of the Council’s key objectives; specifically in relation to the Community Plan, Shared Commitments, Single Outcome Agreement a

Childcare & Activities Host, Immediate Start! EU Nationals - Work Abroad.

Learning & Development Data Analyst.At Barchester Healthcare, we are committed to developing our people and creating a culture of continuous learning across our organisation.We are looking for a Learning & Development Data Analyst to join our L&D team and play a key role in ensuring the accuracy, in

Applications for this post will only be accepted from current employees of West Lothian Council (this includes casual and agency staff who are currently undertaking work for us).You will support the Passenger Transport Manager in ensuring that the council’s passenger transport services are support