Talentmark

Talentmark are recruiting for a QC Analyst, for a permanent position , to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire. Role: This job is responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times. Key duties will include: Test all materials according to agreed specifications and procedures. Maintain and calibrate all laboratory equipment. Maintain all laboratory Quality Systems, raise and support the investigation of deviations. Write, under supervision, all SOPs associated with QC support. Support the preparation and hosting of competent authority inspections, including preparation for internal and external audits. Support technology transfer projects and in particular any QC aspects of these. Your Background: Educated to degree level or above in life science or a related field. Previous QC experience in a pharmaceutical Laboratory with extensive knowledge of Quality Control, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical products. Ability to interpret complex data and present key findings. Demonstrated Knowledge, understanding and application of GMP Guidelines and Regulations. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 71608 in all correspondence.

Talentmark are recruiting for an AI Automation/Application Engineer to join a company in the pharmaceutical industry on a contract basis for 12 months . This role is hybrid, with the office in Welwyn Garden City. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Salary: .04 per day (PAYE) or 500 - 600 per day (Umbrella/Ltd) . This contract can be outside of IR35. Rates are dependent upon experience. AI Automation Engineer Role: Build and maintain AI skills and agents that take on repetitive work, such as self-assembling reports and presentations, document checks and request-to-system workflows Develop agentified dashboards in R Shiny (or Shiny for Python) with built-in AI assistants that explain trends, flag issues and answer questions Automate manual, repetitive steps across business tools, documents and spreadsheets, including supervised automations where people review and approve outputs before use Build scheduled data pipelines and integrations that pull, clean, reconcile and combine data from business systems to create reliable insights Write tested, version-controlled code and clear documentation, and produce validation evidence for regulated use cases with the Senior AI Solutions Engineer and Quality & Compliance Run user testing, train business teams, gather feedback and iterate quickly, tracking usage and time saved. Maintain live tools and keep them working as source systems change. Your Background : A degree in Computer Science, Engineering, Data Science, Information Systems or a related field, or equivalent practical experience Substantial experience building data applications, automations or internal tools used by business teams Strong Python for scripting, automation and data processing (pandas, requests, testing), plus solid R with experience building and deploying Shiny applications Good SQL and experience integrating systems through REST APIs Practical experience building with LLM APIs or AI coding tools, including prompt design and structured outputs Comfortable with Git and working iteratively with non-technical users, translating their needs into working tools. Nice to have: Snowflake or another cloud data warehouse, AI agents and agent frameworks (e.g. LangGraph), Docker and AWS deployment, pharmaceutical R&D or GxP experience, and a GitHub profile or portfolio. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this AI Automation/Application Engineer role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71655. 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 Clinical Development Lead to join a company in the pharmaceutical industry on a contract basis for 12 months . This role is hybrid , with 3 days a week on-site at Burgess Hill. Salary: 49.73 - 65.00 per hour (PAYE) or 65.86 - 86.09 per hour (Umbrella/Ltd) Rates are dependent upon experience. Clinical Development Lead Role: Lead end-to-end documentation strategy and lifecycle management to support regulatory submissions. Work with Clinical Development Leaders, Clinical Operations, Regulatory, Quality, Labelling and R&D to produce Clinical Study and Performance Evaluation documentation. Author, review and finalise critical documents, including IVDR Performance Evaluation documentation, Protocols, Clinical Study Reports and Investigator Brochures. Run scientific literature reviews and synthesise complex laboratory and clinical data into clear, regulatory-ready reports. Your Background : A PhD or an advanced degree in Pharmacy/Life Sciences or a related clinical research field. Demonstrable experience in scientific or medical writing, in industry or academia, ideally with peer-reviewed publications. Strong organisation, project management and cross-functional communication skills, with the ability to lead multiple complex projects at once. Proficiency with generative AI tools for literature synthesis and drafting. This includes verifying outputs against primary sources, preventing hallucinations and upholding data privacy standards. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Clinical Development Lead role, please contact the Key Accounts Team on (phone number removed) or email (url removed) . Please quote reference 71653 . 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 Procurement Associate to join a company in the pharmaceutical industry on a contract basis for 8 months initially . This role is hybrid, with 3 days a week in the Basingstoke office. Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs. Salary: 21.16 to 27.16 per hour, PAYE Rates are dependent upon experience. Procurement Associate Role: Plan and run tendering processes, from building the strategy through to choosing the right supplier, delivering on time and at best value. Agree strong commercial terms and develop contracts within your categories. Work with business owners to get the most from suppliers, and act as the escalation point for contract or performance issues. Give commercial guidance to internal teams and help shape preferred supplier lists and category strategies. Identify and reduce risks linked to third-party suppliers, and make sure procurement processes and financial authorisation policies are followed. Your Background : Proven background in category management and running competitive sourcing processes. Demonstrable experience of working directly with external suppliers and agreeing contracts. Able to review different sources of information, make clear recommendations, and build relationships at all levels, with excellent written and spoken English. Comfortable managing multiple projects and internal customer groups at once, with minimal guidance. Confident using Microsoft Office and AI tools. Desirable: CIPS qualification (or equivalent), experience in a pharmaceutical, healthcare or other regulated environment, and a degree or equivalent professional experience. Apply: For more information, or to apply for this Procurement Associate role please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71571. 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 Nutrition Strategy & Communications Manager to join a leading global food brand company on a contract basis for 12 months. This role is hybrid, based in Birmingham . Company: Our client is a world leader in food, confectionery and beverages. They operate in over 70 countries worldwide and currently have almost 100,000 talented employees working for them. They have a strong foundation of iconic brands, which makes them a very established company within the field. The client's aim is to have a positive impact on the customers and the planet, while still ensuring business success. Salary : 28.37 to 35.47 per hour PAYE. Rates are dependent upon experience. Nutrition Strategy & Communications Manager Role: Garner expert knowledge of the UK regulatory environment around food, drink, health and wellbeing interventions, including HFSS. Track the changing external landscape and advise internal stakeholders on the opportunities and implications for the business. Develop and support nutrition and wellbeing message and claim development for key brands, working with brand teams, consumer insights, regulatory affairs, nutrition research and legal, adapting global guidance for local context. Provide marketing teams with nutrition-related support across packaging, advertising, websites and materials for healthcare professionals. Support development of scientific communication materials for professional and consumer audiences, and support health influencer outreach and nutrition conference strategies. Support internal nutrition and wellbeing education programmes to increase employee knowledge and awareness. Your Background: Minimum BSc (Hons) degree in Human Nutrition or a related field; a Master's degree is preferred. At least 5 years' food industry experience, with robust expertise in human nutrition and awareness of the latest food and nutrition trends. Strong communicator able to translate scientific knowledge into clear, credible messaging and deliver confident presentations. Proven project management skills with the ability to multi-task, prioritise and meet multiple deadlines in a fast-paced environment. Strong collaboration and stakeholder management skills, able to work autonomously across cross-country and cross-category teams. Apply: For more information, or to apply for this Nutrition Strategy & Communications Manager role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71284 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 currently recruiting for a Stores Coordinator and Service Support role in Hatfield on a permanent, full-time basis. Salary: Competitive salary based on experience Location: Hatfield, Hertfordshire Working Hours: Monday - Friday 7:30-4 Key Responsibilities: Manage engineering stores and maintain accurate GMP and non-GMP inventory records, ensuring stock accuracy, traceability and compliance with GxP requirements. Receive, inspect, store and issue engineering materials, spare parts and consumables, monitoring stock levels and coordinating procurement to prevent shortages. Provide Engineering Service Desk and CMMS support, including logging and prioritising work requests, Support audits, inspections and compliance activities by maintaining accurate documentation, coordinating contractor and visitor inductions, and assisting with engineering performance reporting. Skills & Requirements: Previous experience in inventory management, preferably within a pharmaceutical environment, with the ability to maintain accurate stock records and manage inventory movements. Knowledge of pharmaceutical regulatory requirements, including GxP, GMP, COSHH, waste management and Health & Safety procedures. Working knowledge of CMMS for inventory stock control and asset management, with experience using SAP, Ariba, Maximo, Airsweb or similar business systems. Strong organisational, communication and time-management skills, with excellent attention to detail and the ability to prioritise tasks, work independently and solve problems effectively. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference 71560 in all correspondence.

Talentmark are recruiting for an Administrative Assistant to join a company in the pharmaceutical industry on a contract basis for 12 months . This role is hybrid, based at two sites every week - 2 days in Basingstoke and 2 days in Bracknell, with 1 day per week working from home. Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs. Salary: 15.12 - 20.16 per hour, PAYE Rates are dependent upon experience. Administrative Assistant Role: Manage the diaries of four senior technology leaders, resolving conflicts and prioritising by business impact. Book international and domestic travel, including flights, hotels and rail, with an eye on policy, cost and itinerary resilience. Run end-to-end logistics for in-person meetings and visits, including visa invitation letters, accommodation, transfers, catering and meeting rooms. Support town halls, team events and celebrations, and prepare agendas for monthly team meetings. Handle purchase order requests, the monthly PO review and distribution list maintenance. Your Background : Proven experience as an executive assistant supporting multiple senior leaders at director level or above, with strong Outlook calendar management across time zones. Experience booking complex international travel and organising multi-day events for global attendees. Working knowledge of purchase-to-pay processes, ideally with Concur, Ariba or Workday (pharma or regulated environment experience a plus). Excellent discretion with confidential information, and clear written and verbal communication. Proactive, calm under pressure and self-directed, with a collaborative, adaptable approach and enthusiasm for AI and productivity tools. Apply: For more information, or to apply for this Administrative Assistant role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71576 . 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 Downstream Processing Scientist to join a company in the animal health and pharmaceutical industry on a contract basis for 6 months. This role is fully site-based in Speke, Merseyside. Company: Our client specialises in animal health. They advance their vision of food and companionship, enriching life by developing innovative solutions that protect and enhance animal health. Salary: From 15.38 to 20.51 ph PAYE Rates are dependant upon experience Downstream Processing Scientist Role: Plan and execute laboratory and pilot-scale studies through hands-on experimentation. Deliver downstream purification processes to support clinical programs and business milestones. Utilise statistical tools to design, analyse, and interpret complex data sets. Provide technical and operational expertise in downstream processing. Support the maintenance and readiness of downstream laboratory equipment. Your Background : Hold a relevant scientific degree, or have equivalent working experience. Some previous experience in biopharmaceutical downstream development or manufacturing. Familiarity with a range of techiques/sytems such as the following would be an advantage: FPLC Chromatography (AKTA systems with Unicorn Software) Familiarity with GxP Standards. Depth Filtration Process Scale Up Apply: For more information, or to apply for this Downstream Processing Scientist , please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71491. 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 Senior Scientist/Associate Principal Scientist - Process Chemistry on behalf of a growing drug development partner who support clients across the pharmaceutical and biotech sectors. This role will be based in Cardiff, on a permanent basis. Responsibilities: Working collaboratively on a range of client programmes, applying technical expertise to solve challenging problems across drug discovery and development. Technically leading projects/work packages for our customers, under the guidance of a senior manager. Designing experimental work for yourself, and other scientists (as required), conducting laboratory work and interpreting results to draw conclusions. Applying scientific judgement to troubleshoot and solve technical challenges. Delivering project milestones to agreed timelines and quality standards. Presenting data clearly to project teams and clients, both written and verbal. Supporting and mentoring more junior Scientists. Maintaining excellent standards of documentation, data integrity, and laboratory safety. Your Background: Educated to MSc or PhD level in a relevant chemistry field. Significant relevant industry experience in process chemistry in drug discovery. Experience with late-stage process optimisation, encompassing activities such as impurity fate and purge, PAR/NOR studies, robustness studies, technology transfer and/or support of manufacturing campaigns. Experience in a CRO environment would be beneficial. Strong experimental design and data interpretation skills. The ability to work independently while contributing effectively to teams. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference 71494 in all correspondence.

Talentmark are recruiting for a Senior Bioinformatician to join a company in the pharmaceutical industry on a contract basis for 12 months. This role is hybid with 2/3 days on site in Bracknell and the rest home working. Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs. Salary: 36.84 to 49.13 ph Rates are dependent upon experience. Senior Bioinformatician Role: Analyse large-scale single-cell, bulk transcriptomics and other omics datasets. Develop new computational methods that extract biological insight from them. Build scalable, well-tested and documented software and workflows for atlas-scale data (millions of cells) and high-dimensional proteomics. Act as the analytical point of contact within multidisciplinary scientific collaborations from analysis plan through to publication or portfolio decision. Translate complex findings into clear recommendations for project teams and leadership. Your Background : PhD in bioinformatics, computational biology, statistical genetics, statistics or a related quantitative discipline, or an MSc with equivalent industry experience. Hands-on experience analysing single-cell or single-nucleus transcriptomic data at scale, including QC, integration, annotation and differential analysis. A demonstrated track record of developing computational methods or tools. Experience with spatial transcriptomics or spatial proteomics platforms, such as Visium, Xenium, MERFISH or CosMx. Experience with deep generative or foundation models for single-cell data, such as scVI-tools, scGPT or Geneformer. Apply: For more information, or to apply for this Senior Bioinformatician role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71497. 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 is recruiting a Clinical Bioinformatician to join a global pharmaceutical company on a contract basis, initially for approximately 6 months. This role is hybrid, with 3 days per week in the office in Slough. Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future. Salary: From 36.55 per hour (PAYE) or 50.27 per hour (Umbrella) Clinical Bioinformatician Role: Process, analyse and interpret omics data from clinical portfolio studies to uncover biological mechanisms, treatment effects and safety signals. Develop analysis methods and pipelines using state-of-the-art tools and technologies. Document code and analyses, ensuring reproducible results in line with best practice for patient-level data. Write clear, well-structured reports covering methods and results. Contribute to scientific publications, including conference abstracts, presentations and manuscripts. Your Background : Master's degree or PhD in a relevant field, with experience analysing omics data (industry experience preferred). Strong expertise in analysing large bulk and single-cell RNAseq datasets and deriving biological insights (spatial, epigenomic and proteomic experience is a bonus). Skilled in functional interpretation of omics data, e.g. pathway enrichment, functional module detection, causal reasoning. Excellent computational skills: R proficiency, HPC/Unix, cloud or pipelining platforms and Docker (DNAnexus is a plus). Solid grounding in statistics and data visualisation, plus the ability to communicate findings clearly to expert and non-expert audiences (publication experience preferred). Company: Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future. Apply: For more information, or to apply for this Clinical Bioinformatician role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71373. 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 is recruiting for a Senior / Laboratory Manager to join a specialist organisation in the UK. This is a leadership role, supporting the Director of Toxicology in driving laboratory performance, business growth and the development of new services. Senior / Laboratory Manager Role: Support the development and delivery of the toxicology strategy and deputise for the Director when required. Lead and develop teams of supervisors, scientists and administrators, driving performance and employee development. Improve laboratory productivity, efficiency and service quality within a high-throughput environment. Contribute to commercial projects, tender bids and the development of new products and services. Drive continuous improvement, cost reduction and the adoption of new technologies. Support compliance with ISO 17025, ISO 9001 and ISO 14001 standards, working closely with the QHSE Manager. Collaborate across the business to deliver strategic projects and growth objectives. Your Background: Hold a degree or higher qualification in a relevant scientific discipline. Have experience in a managerial / strategic role, ideally within toxicology or laboratory services. Experience in a high-throughput, regulated or accredited environment. Strong commercial and financial acumen, including P&L understanding. A track record of improving operational efficiency and delivering projects. Excellent leadership, communication and problem-solving skills. Company: Our client provides specialist toxicology laboratory services, with a focus on scientific excellence, quality, customer service and commercial growth. This is an opportunity to play a key role in the strategic development and operational performance of its toxicology function. Apply: For more information or to apply, please contact Alex Willson on (phone number removed) or email (url removed). Please quote reference 71486. It is essential that applicants hold entitlement to work in the UK.

Talentmark are recruiting for a Senior R&D Scientist to join a company in the medical devices industry on a contract basis for 12 months. This role is fully site-based in Motherwell. Salary: 24.52 - 26.56 per hour PAYE Senior R&D Scientist Role: Execute complex, high-quality experimental workstreams from concept through to final recommendation and design transfer. Analyse and interpret complex data from multi-factorial experiments. Present project updates and technical findings effectively to stakeholders Apply Design for Manufacture (DFM) philosophy to optimise product formulations and characterisation processes Champion laboratory excellence by creating a working environment that proactively supports compliance, including GLP, GMP, and GDP standards Your Background: Hold a Master's degree in a life science subject. A BSc will be considered if coupled with industry experience. Proven knowledge of diagnostic immunoassay technology and the ability to follow or improve complex experimental protocols. Strong computer literacy and data analysis skills, with a track record of delivering accurate results on time. Excellent communication skills, specifically in writing technical documentation and laboratory records. Experience with particle-based immunoassays, fluorescent detection, whole-blood assays, and working within GMP/GLP/GDP or biohazard environments is preferred. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Senior R&D Scientist, please contact Mary Bolt on (phone number removed) or email (url removed). Please quote reference 71382 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 an Analytical Laboratory Technician to join a resin and composites company on a contract basis for 6 months . This role is fully site based in Heanor, Derbyshire . Company: Our client is an advanced materials and speciality chemical company focused on the manufacture of resins. Salary: 13.70 per hour Salary is dependent on experience. Analytical Laboratory Technician Role: Analytical testing of epoxy resins mostly by thermal analysis and HPLC but the job could also involve FT-IR. Data gathering, logging results and paperwork associated with testing. General housekeeping of laboratory. Opportunity to be involved in method improvements. Your Background : A-levels or similar qualifications in Chemistry, Maths, Physics or similar. Experience with the following analytical techniques: HPLC, FT-IR or any thermal analysis would be advantageous. Good eye for detail & team player. Apply: For more information, or to apply for this Analytical Laboratory Technician position please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71306. 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 Safety Data Specialist to join a company in the pharmaceutical industry on a contract basis for 12 months. This role is hybrid, 3 days per week in Welwyn Garden City and 2 days working from home. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Salary: 29.85 ph to 35.82 ph PAYE or 40 ph to 48 ph via umbrella Rates are dependent upon experience Safety Data Specialist Role : Ensure safety data is processed and reported in a high-quality and compliant manner. Perform oversight of the service provider who executes individual case safety reports (ICSR) tasks. Answering queries and proactively sharing your subject matter expertise with stakeholders. Identifying root causes of non-compliance to agree Corrective Actions and Preventative Actions (CAPAs. Impact assessment of new / updated regulatory requirements. Conducting process reviews to design and implement process improvements. Your Background : Hold a relevant degree or have equivalent working experience in pharmacovigilance (PV). Working experience in PV within the pharmaceutical industry. Excellent understanding of international regulations, including ICH, EU GVP modules and FDA. Profound knowledge of topics and regulations within ICSR case processing. Great stakeholder/relationship management skills Apply: For more information, or to apply for this Safety Data Specialist, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71646 . 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 Customer Care Coordinator to join a recycling solutions company on a permanent basis. Salary: Competitive depending on experience. Location: Onsite based Dungannon, Northern Ireland. The successful candidate will be responsible for handling customer care tickets through to resolution or escalation, providing efficient operational support and delivering best-in-class service to customers. Key duties will include: Contact customers to clarify issues, provide regular updates on job progress, and deliver excellent service support . Book engineer works, maintain and update the master schedule, and report new bookings to line management for review. Invoice completed jobs daily, pass processed worksheets for billing, and chase outstanding PO numbers for completed works. Ensure Risk Assessments and Method Statements (RAMS) are sent to site and handle the hiring and off hiring of plant equipment. Perform other administrative and supportive duties as required by management. Your Background and Skills: Minimum of 1 year of experience in a Customer Service or Administrative role. Minimum of 5 GCSEs (or equivalent) including Mathematics and English at Grade C / Grade 4 or above. Strong interpersonal and communication skills. Excellent attention to detail and accurate data entry skills. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 71640 in all correspondence.

Talentmark are recruiting for a Senior HR Associate to join a company in the pharmaceutical industry on a contract basis for 12 months . This role is hybrid, with at least 3 days per week at the Basingstoke office. The working hours for the role are from 9:00 AM to 5:00 PM, Monday to Friday, with a daily 30-minute lunch break. Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs. Salary: 21.67 - 28.27 per hour, PAYE Rates are dependent upon experience. Senior HR Associate Role: Run UK HR operations: Deliver local HR admin processes across the employee life cycle, including complex and sensitive cases, and cover the admin team during absence and peak periods. Be the expert adviser: Advise employees, managers and HR on policies such as family leave, sick pay, benefits, pensions, company car, mobility and immigration. Own and improve processes: Document and control UK processes, keep them compliant with UK laws and company policies, and use demand data and AI tools to fix root causes and improve self-service. Manage providers and data: Own the relationship with third-party providers and the accuracy of HR data feeds, and act as the UK HR data privacy contact. Support the team: Coach the HR admin team and document processes so others can cover. Your Background : Experience: Degree or equivalent, plus substantial experience running HR admin processes in a complex organisation. Legal knowledge: Working knowledge of UK employment law (family leave, sick pay, working time, right to work, data protection). Analytical and AI skills: Strong data analysis, advanced Excel, and the ability to use AI tools to work more efficiently. Improvement track record: A measurable improvement to a process you personally delivered, with a customer-focused approach. Ownership and discretion: Proactive in driving issues to resolution, comfortable balancing hands-on processing with improvement work, and trusted with confidential information. Ideally have experience with using Workday and case management systems, pensions/benefits/mobility experience, third-party provider management, Lean or Six Sigma, CIPD. Apply: For more information, or to apply for this Senior HR Associate role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71462. 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 Production Support Operator on behalf of a Leading UK Specialist Manufacturing Company. This role will be based at their site in Standish, working 12-hour day shifts, from 6am to 6pm Monday to Thursday on a permanent basis. Salary The salary for this role will be competitive based on experience. The Role Your main responsibility will be to support the safe and efficient operation of the Production Department, including production planning, material handling, as well as following strict Safety, Quality and Compliance Regulations. Responsibilities: Operate and monitor the filtration press, completing accurate records and maintaining production schedules in a timely manner. Safely operate a Counterbalance Forklift Truck to transport raw materials, intermediates and finished goods. Assist with stock checks and inventory accuracy, to ensure consistent levels of stock ahead of manufacturing. Maintain high housekeeping standards across production, including keeping production areas tidy and supporting with waste segregation. Work in accordance with COMAH requirements and comply with all Quality, Environmental and Health & Safety procedures. Essential Skills: Forklift truck license. Ability to follow manufacturing protocols. Good understanding of sampling and product testing. Willingness to comply with safety and quality regulations, including use of PPE. Previous Manufacturing / Production experience is preferred, specifically in the Chemical industry. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference 71423 in all correspondence.