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Senior AI Engineer / AI Architect - Contract Healthcare & Life Sciences | Competitive Day Rate We're looking for an experienced AI specialist to design and deliver production-ready AI solutions within Healthcare and Life Sciences. This contract could suit a Senior AI Engineer, AI Architect, Technical Lead or GenAI Consultant with experience across healthcare, pharmaceuticals, biotechnology, medical devices or health technology. What we're looking for Experience delivering AI solutions within Healthcare or Life Sciences Strong Python and modern AI framework expertise Hands-on experience with LLMs, Generative AI, RAG and AI agents Knowledge of Azure, AWS or GCP Experience taking AI solutions from concept into production Understanding of sensitive data, security, governance and responsible AI Strong technical and stakeholder communication skills You do not need to match every requirement. However, genuine Healthcare or Life Sciences experience is essential. If you're an experienced AI contractor looking for your next project, please apply or get in touch for a confidential conversation. JBRP1_UKTJ

Location: Hatfield, Hertfordshire - 5x per week Industry: Pharmaceuticals The Opportunity: Our client is an established international pharmaceutical organisation with a growing UK and European presence. They are seeking a highly experienced, UK-registered Qualified Person (QP) to take responsibility for QP batch certification and lead the UK Quality Management System. This is a senior and highly accountable position, responsible for ensuring the quality, safety and regulatory compliance of medicinal products entering the UK market. Working closely with UK senior leadership and international Quality, Regulatory, Operations and Supply Chain teams, the successful candidate will play an important role in maintaining compliance, supporting new product launches and ensuring continuity of pharmaceutical supply. Key Responsibilities: QP Batch Certification & Release Fulfil the statutory responsibilities of a Qualified Person under the Human Medicines Regulations 2012. Review and certify imported batches of finished medicinal products in accordance with GMP, Marketing Authorisations and UK regulatory requirements. Oversee batch certification and final market release for products manufactured outside the UK. Ensure appropriate analytical, microbiological and physical testing has been completed prior to release. Oversee Analytical Method Transfers between international manufacturing/QC teams and UK or European testing laboratories. Review and approve Out-of-Specification results, deviations, investigations and CAPAs. Act as RP/RPi for relevant UK/EU activities where required. Quality Management System & GDP Own, maintain and continuously improve the UK Quality Management System. Ensure continued compliance with GMP, GDP and applicable MHRA requirements. Lead the development and review of SOPs, Change Controls, Deviations and CAPAs. Maintain the QMS in line with evolving UK pharmaceutical regulations. Conduct and oversee audits of external manufacturing organisations, laboratories, warehouses, logistics providers and other suppliers. Maintain appropriate Quality Technical Agreements with external partners. Lead quality complaint and product recall processes, including appropriate MHRA reporting. Develop and deliver ongoing GxP training to relevant UK employees. New Product Launches & Supply Lead the Quality workstream supporting new pharmaceutical product launches into the UK. Ensure regulatory approvals, manufacturing documentation, testing requirements and batch release documentation are in place ahead of launch. Work cross-functionally with Regulatory, Commercial, Quality, Operations and Supply Chain teams. Support supply continuity and help minimise the risk of critical stock shortages. Review shipping validation, temperature monitoring and relevant customs and quality documentation for imported products. Qualifications & Experience: The successful candidate will be required to demonstrate A relevant university degree in Pharmacy, Pharmaceutical Chemistry, Biology, Chemistry or another permitted scientific discipline . Formal registration and recognition as a Qualified Person in the UK , eligible to be named on a UK Manufacturer's/Importer's Authorisation. Approximately 15 years' experience within pharmaceutical Quality Assurance and/or Quality Control . At least 23 years' active batch release experience as a named QP under an MIA licence . Strong working knowledge of UK/EU GMP, GDP and Human Medicines Regulations 2012 . Demonstrable experience supporting and managing MHRA inspections , including responses and remediation of observations. Strong knowledge of auditing, analytical and microbiological testing, stability data and analytical method transfers. Experience managing deviations, investigations, Change Controls and CAPAs. Strong cross-functional communication and stakeholder management skills. Desirable Experience Experience within a generic pharmaceutical import and wholesale environment . Experience managing products manufactured at third-country sites. Active GPhC registration or equivalent professional registration in chemistry or biology. Experience across oral solid dosage products, sterile products and oral solutions. Experience using pharmaceutical ERP and electronic document management systems; SAP experience would be advantageous . TPBN1_UKTJ

An exciting opportunity has been created for a Procurement Lead to join a global leader in high-technology medical products. The Procurement Lead is responsible for managing day to day procurement activities and supplier performance across a global supply network, with a primary focus on suppliers and contract manufacturers in order to procure finished goods. The role will execute sourcing strategies set by the Procurement Director, optimise total cost, and ensure continuity of supply. This is a hybrid role with 3 days a week at their head office in Hemel Hempstead Key responsibilities of the Procurement Lead: Lead commercial management for a defined portfolio of suppliers and CMOs, owning pricing, terms, and contract implementation within strategies set by the Procurement Director. Run RFx and negotiations to secure competitive pricing and total cost of ownership against agreed budgets and savings targets. Analyse and challenge key cost drivers (including upstream raw materials) and propose mitigation actions where cost or availability risks emerge. Act as primary procurement contact for suppliers, maintaining strong relationships and alignment to service, quality, and compliance expectations. Review supplier performance across cost, quality, OTIF, and responsiveness, driving corrective actions and continuous improvement with cross‑functional stakeholders. Assess supply chain risk across tier‑1 and key tier‑2 materials, escalating issues and supporting dual‑sourcing or re‑sourcing decisions where necessary. Support annual cost‑improvement and value‑creation targets for suppliers by identifying opportunities and delivering agreed initiatives. Work closely with Quality, Regulatory, Planning, and Commercial teams so suppliers support launches, change controls, and ongoing service requirements. Lead or support procurement workstreams for change controls, product transfers, cost‑improvement projects, validation work, and supplier audits. Skills & experience required of the Procurement Lead: Over 5 years' experience in procurement, sourcing, or supply chain roles, including direct materials or contract manufacturing in medical devices, pharmaceuticals, healthcare, cosmetic or FMCG. (5+ years direct procurement experience is essential) Experience working with suppliers and stakeholders across different countries or regions, with proven ability to manage cross‑cultural relationships and time‑zone differences. (cross‑cultural experience is good to have) Exposure to NPD, change control, or technical transfer projects, working cross‑functionally with Quality, Regulatory, and R&D or Technical functions. Solid understanding of contract manufacturing environments, core commercial and contractual terms, and supply risk management principles. (Experience either in manufacturing environment or working with manufacturing partnerships is essential) CIPS or equivalent professional procurement qualification are desirable Package of the Procurement Lead Salary £55-£60,000 Bonus Pension Private Health Softer Benefits This Procurement Lead position would suit a procurement or purchasing professional who has held roles such as Senior Buyer, Lead Buyer, Principle Buyer, Category Manager or Procurement Manager

Contract Maintenance Engineer - Hatfield Hertfordshire (Outside IR35) Rate: £37ph Outside IR35 LTD or Umbrella Hours:8-hour shifts - Monday to Friday and overtime Length: 6 months Start: ASAP About the Role We're looking for an experienced Contract Maintenance Engineer to join a manufacturer in Hatfield. This is a hands-on a contract where you'll keep high-speed production lines running smoothly in a modern, well-invested site. Why Apply? Outside IR35 6 month contract Supportive team with good feedback from current engineersKey Duties Preventive and reactive maintenance of machinery Working 8 hour rotation shifts, mornings, afternoons, nights. Mechanical/electrical fault finding and repairs Work on conveyors and automated production equipment Minimise downtime and support continuous improvementWhat We're Looking For Mechanical or Electrical qualification (Apprenticeship / NVQ / C&G) Hands-on experience as a Maintenance Engineer in manufacturing Multi-skilled preferred (mechanical & electrical) Ability to use initiative in a fast-paced environmentApply Now If this Maintenance Engineer role sounds right for you, contact Simon on (phone number removed) or email (url removed). Commutable from Hatfield, St Albans, Bedford, Stevenage, Welwyn Garden City, Hertford, Bishop Stortford, Standsted, Letchworth, Luton, Biggleswade, Watford, Potters Bar, Enfield, Harlow, Cheshunt, Hoddesdon, Borehamwood, Epping, other parts of London, Hertfordshire, and Essex Proactive (About Us) We specialise in FMCG Manufacturing, Food & Beverage Manufacturing, Pharmaceuticals Manufacturing, Automation and Machinery OEMs & System Integrators. Our FMCG division is structured into niche specialist teams across Engineering, Operations (Technical & Production), Projects, and Senior Appointments. With a network of offices in the City of London, West London, Leeds, Milton Keynes, Birmingham, and an international reach, Proactive supplies both permanent and contract workforces to clients nationwide. Backed by a proven track record of successful partnerships, we understand the challenges you face and work closely with you to ensure the right fit for every role Proactive Global is committed to equality in the workplace and is an equal opportunity employer. Proactive Global is acting as an Employment Business in relation to this vacancy

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