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Head of CQV Location: Slough, UK In the role of Validation Lead at Lonza AG, you have the exciting opportunity to lead and oversee our operational Validation teams within the Technical Services function. This position is vital in ensuring the flawless implementation and adherence of our software, equipment, and processes. By joining our team, you will be part of a global leader in life sciences, promoting innovation and making a meaningful difference in the world. Your expertise and leadership will be crucial in providing exceptional service to both internal and external collaborators. Key responsibilities: • Lead and guide the Validation Teams to guarantee alignment with the Technical Services strategy in terms of delivery, performance, and compliance., • Maintain the Site Validation Master Plan and govern Validation procedures to meet current regulatory requirements, internal global standards, industry standards, and business improvement projects., • Interact with internal and external clients and oversight bodies to guarantee that customer requirements match operational implementation, stepping in when needed to address issues., • Establish and maintain positive connections with collaborators and cross-functional departments, including Manufacturing and Development Services groups., • Supervise validation consultants and contractors throughout the completion of site projects, tracking important metrics to guarantee performance and value for money., • Contribute to Global and Local initiatives where Validation can directly contribute to or benefit from the initiative's implementation.Key requirements:, • Demonstrated gravitas, intellectual capability, and daily operational grip to gain immediate respect and credibility across the organization, from the shop floor to the site leadership team., • A proven track record of successfully implementing change and achieving goals with tenacity., • Strategic problem solver with a passion for improvement, combined with an execution approach., • Intellectual ability to think abstractly and creatively to resolve problems and achieve practical results., • Proven ability to lead, mentor, and encourage individuals and teams to set and achieve breakthrough performance goals., • Ability to manage multiple projects simultaneously through to delivery., • Strong business and interpersonal skills with persuasive communication abilities – written, oral, and active listening – to influence peers and colleagues. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. #LI-WF1

Are you an experienced Quality Assurance professional? Do you have a background in a Pharmaceutical or Clinical Development setting? If so, this could be the perfect opportunity for you! We are recruiting for a Senior Process Quality Excellence Specialist to join a leading multinational biopharmaceutical client based in Berkshire. The successful candidate will support the Head of Process Quality Excellence in developing and maintaining its clinical quality systems/procedures and ensuring quality and compliance risks are appropriately identified and mitigated. Candidates will need experience and focus on GCP, GLP and PV regulations and guidance. This is a contract position, inside IR35, offered initially for 12 months on a hybrid basis. Responsibilities: • Support the Head with quality and compliance infrastructure development, assist with creation/revision of appropriate quality and compliance policies, SOPs, processes, and best practices as needed., • Work in collaboration with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for ICH, GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness., • Lead and drive inspection readiness activities across functions working closely with the relevant inspection teams., • Participate in audit and inspection planning with global quality., • Represent or ensure representation including preparation during audits/inspections / on-site by internal and external parties., • Support staff with audit/inspection responses, where required. Requirements: • 8+ years of pharmaceutical experience, preferably in a global quality assurance or a clinical development setting., • In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections., • 2+ years of experience in SOP writing essential.

Contract: 9-month initially, with possibility of extension Location: Fully on-site in Slough Company: A global pharmaceutical company Job Description Role Purpose & Scope • Join the QA Operations Documentation Control Team, supporting quality assurance activities across the organization., • The primary responsibility is to perform batch consolidation (auditing) for QC Biochemistry and QC Microbiology testing related to Drug Product (DP) and Drug Substance (DS)., • This role involves coordinating QC testing documentation and independently verifying that all required activities are completed and release specifications are met., • Proactively issue GMP documents and labels to Manufacturing in line with scheduled timelines provided by internal departments. Key Responsibilities • Collaborate with internal teams to gather necessary information and maintain strong interdepartmental communication., • Support continuous improvement initiatives within QA quality systems and processes., • Identify and implement enhancements in safety, GMP compliance, and operational efficiency., • Conduct batch consolidation for QC Biochemistry and Microbiology testing of DP and DS., • Prepare documentation for audits and provide consolidated QC data during customer and regulatory inspections., • Contribute to projects aimed at maintaining and improving QA systems., • Apply quality procedures to identify non-conformances and assist in resolving issues., • Issue approved GMP documents for Manufacturing, ensuring accuracy and adherence to deadlines., • Print and verify labels for manufacturing use, including finished product labels., • Issue GMP-compliant logbooks as required., • Manage quality records such as Deviations, CAPAs, Change Controls, and Investigations., • Author, review, and approve GMP documentation., • Prioritize tasks to meet critical deadlines., • Maintain training compliance, ensuring all required modules are completed before performing assigned duties., • Perform additional tasks as required. Key Stakeholders • Quality Control, • Manufacturing, • Quality Assurance and Qualified Persons (QPs) Required Skills & Competencies Skills • Proficient in MS Office (Word, Excel, Access, Outlook) and database systems, • Strong verbal and written communication, • Risk-based decision-making capabilities, • Familiarity with Pharmaceutical Quality Systems (PQS), • High attention to detail and accurate data entry, • Effective workload prioritization and scheduling, • Ability to meet strict deadlines, • Strong organizational and planning abilities Competencies Agility • Learns from experience and adapts to change, • Understands strategic goals and contributes to business success, • Actively participates in team efforts, • Understands customer needs and acts on feedback, • Delivers goals consistently while monitoring KPIs, • Takes ownership of safety and personal development, • Fosters a positive and dependable team environment Qualifications Education • Prior experience in QA and GMP environments, • Strong attention to detail and accurate data entry skills required

About Us: CliniMed Limited is a leading name in Healthcare and Medical Equipment industry. We are a group of companies founded in 1982 following the acquisition and formation of number of additional companies within the group. We're a fast-growing and dynamic organization that's dedicated to making a difference in the lives of our customers. Through the development of innovative healthcare products and exceptional customer services, we are committed to improve lives of our customers exceeding their expectations. Job Summary: As a Graduate QARA Associate, you will play a vital role in supporting and maintaining our Quality Management System (QMS), ensuring compliance with ISO 9001, ISO 13485, and relevant medical device regulations. This is a hands-on opportunity to gain practical experience in quality assurance, regulatory compliance, and continuous improvement within a dynamic and supportive environment. You will receive tailored training, mentoring, and the chance to contribute to meaningful projects across the business. The role involves close collaboration with cross-functional teams, so strong communication skills and a proactive approach are essential. This is an excellent opportunity for a motivated graduate with a keen analytical mindset and a strong desire to learn. It provides a solid foundation for building a successful career in the quality and regulatory field within the medical devices industry. Main Duties & Responsibilities: • Support the day-to-day coordination and management of compliance with ISO 9001, ISO 13485, and Quality Management System (QMS) requirements., • Assist in maintaining and updating QMS documentation, including purchase specifications, reference materials, and Standard Operating Procedures (SOPs)., • Participate in internal audits and provide support during external regulatory inspections., • Assist in the investigation and resolution of customer complaints, including responses to technical enquiries., • Contribute to the delivery of training initiatives related to quality and regulatory standards across all levels of the organisation., • Support change management processes to drive continuous improvement and maintain regulatory compliance., • Participate in supplier evaluations and track continuous improvement activities., • Ensure accurate documentation and uphold data integrity across all quality and regulatory functions. Personal Specification: Essential: • Degree or diploma in a scientific, engineering, or quality-related field, or equivalent experience, • Strong interest in quality management, regulatory affairs, and healthcare compliance, • Excellent written and verbal communication skills, • Good IT skills (MS Word, Excel, Office), • High attention to detail with strong analytical and problem-solving abilities, • Organised, with the ability to prioritise and manage workload effectively, • Able to work independently and collaboratively, • Willingness to learn and take on new challenges, • Professional, proactive, and committed to continuous development Desirable: • Awareness of ISO 9001, ISO 13485, or medical device regulations, • Understanding of quality improvement tools (e.g., root cause analysis), • Experience supporting or conducting audits, • Prior experience in a regulated environment (e.g. placement or internship)

About IRIS IRIS Software Group is a leading global provider of mission critical software and services, and one of the UK’s largest privately held software companies. IRIS provides software solutions and services for finance, HR and payroll teams, educational organisations, and accountancy firms that improves efficiency and productivity, taking the pain out of processes and letting professionals focus on the work they love. Our operational software is the invisible, but essential, beating heart of our customers’ businesses, supporting them in a range of objectives, from maintaining legislative compliance, to boosting engagement with stakeholders, to enhancing productivity. It’s vital these mission critical functions work first time, every time. The Role & Purpose We are seeking an exceptional VP, Product - Global Accountancy to lead our product strategy across UK, US, and international markets. This role combines deep accounting domain expertise with strategic product leadership, requiring someone who can translate complex accounting workflows into innovative AI-enhanced product solutions. You will be the strategic thought leader for IRIS's accounting product portfolio while building and leading a high-performing team in a collaborative two-in-a-box partnership with Engineering leadership. The Role in Detail Strategic Thinking & Thought Leadership • Drive product vision and strategy across global accounting markets, staying ahead of regulatory changes, industry trends, and customer needs, • Lead AI transformation strategy for accounting workflows, positioning IRIS products at the forefront of AI evolution in bookkeeping, financial reporting, and compliance, • Serve as the authoritative voice on accounting practices across multiple markets, translating domain knowledge into product roadmaps, • Establish thought leadership through industry engagement, white papers, and strategic partnerships with accounting bodies on the future of AI in accounting, • Build and lead an exceptional product organization including Product Directors, Product Managers, and Product Owners across multiple regions, • Transform product management practices by integrating AI tools for market research, feedback analysis, and roadmap optimization, • Form strategic partnership with VP Engineering, Accounting and VP Engineering, Americas to create seamless product development through shared accountability for outcomes, • Lead executive presentations on product strategy and commercial outcomes while partnering closely with Engineering to present integrated product-technology narratives on delivery progress and AI transformation, • Collaborate on technical architecture decisions that impact product capabilities, scalability, and AI implementation possibilities, • Co-lead strategic delivery planning including quarterly roadmap execution, major release orchestration, and AI model deployment strategies, • Maximise P&L for the global accounting product portfolio, driving growth while delivering on PE investor expectations and value creation milestones, • Lead product discovery and validation with focus on ROI and growth metrics critical to PE stakeholders, • Manage strategic partnerships with key ecosystem players to accelerate market penetration and revenue growth, • Lead acquisition integration from a product perspective, ensuring rapid value realization consistent with PE investment thesis, • Deliver regular reporting to PE stakeholders on product performance and progress against strategic growth initiatives Requirements : Strategic & Domain Experience • 10+ years of product management experience with at least 5 years in senior leadership roles managing global portfolios, • Private Equity portfolio company experience with proven ability to drive accelerated growth and value creation under PE ownership, • Deep accounting domain expertise including GAAP, IFRS, and regulatory requirements across UK, US, and international markets, • Demonstrated success leading large product organizations (20+ people) across geographic regions, • Proven experience in two-in-a-box partnership models with Engineering leadership, showing shared accountability for outcomes, • Strong technical acumen for architectural discussions and product-technology tradeoffs in AI implementations, • Private Equity environment experience including PE reporting, growth acceleration strategies, and acquisition integration timelines, • AI/ML product experience highly desirable, • International business experience navigating different regulatory environments and cultural contexts, • Strategic thinker who anticipates trends and translates them into value-driving product strategies, • Private Equity mindset with commercial acumen, growth urgency, and ability to balance long-term vision with near-term value creation, • AI-forward mindset with curiosity about AI's impact on both customer workflows and product management practices, • Data-driven decision maker balancing quantitative analysis with customer insights and PE-relevant growth indicators, • Excellent communicator capable of inspiring teams and articulating business impact to senior stakeholders and PE investors

Location: Hybrid in Slough with 3 days in the office Company: A global Pharmaceutical Company Senior Quality Specialist The Senior Process Quality Excellence Specialist will assist the Head of Process Quality Excellence in developing and sustaining clinical quality systems and procedures, while ensuring that quality and compliance risks are effectively identified and addressed. This role encompasses all aspects of clinical studies managed by Global Clinical Sciences and Operations (GCSO), with a strong emphasis on Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Pharmacovigilance (PV) regulations and guidelines. Key Responsibilities: • Contribute to the development of quality and compliance infrastructure within GCSO, including drafting and revising policies, Standard Operating Procedures (SOPs), processes, and best practices., • Collaborate with teams across Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure alignment with ICH GCP, GLP, PV standards and applicable local and international regulations, maintaining inspection readiness., • Lead inspection readiness initiatives across GCSO functions, working closely with designated inspection teams., • Participate in audit and inspection planning in coordination with Global Quality., • Ensure GCSO representation and preparedness during internal and external audits and inspections., • Provide support to GCSO personnel in developing responses to audit and inspection findings. Qualifications: • Minimum of 8 years’ experience in the pharmaceutical industry within global Quality Assurance., • Extensive knowledge of GCP and GVP, with practical experience in conducting global audits and inspections., • At least 2 years of experience in SOP development and writing.

• Senior Process Quality Excellence Specialist, • 12 month contract, • Global Pharma The Senior Process Quality Excellence Specialist will support the Head of Process Quality Excellence in developing and maintaining its clinical quality systems/procedures and ensuring quality and compliance risks are appropriately identified and mitigated. Applicants must have comprehensive experience in Good Clinical Practice, Good Laboratory Practices and Pharmacovigilance regulations and guidance. Responsibilities: • Support the Head of Process Quality Excellence in quality and compliance infrastructure development; assist with creation/revision of appropriate quality and compliance policies, Standard Operating Procedures, processes, and best practices as needed., • Work in collaboration with Global Quality, Patient Safety, Regulatory Affairs, strategic partners, and other stakeholders to ensure compliance with International Council for Harmonization of Technical Requirements for Pharmaceutical for Human Use (ICH) GCP, GLP, PV and relevant local and international regulations and to ensure inspection readiness., • Lead and drive Inspection Readiness Activities across all functions working closely with the relevant inspection teams., • Participate in Audit and Inspection planning with Global Quality., • Represent or ensure representation including preparation during audits/inspections., • Support staff with audit/inspection responses, where required. Requirements: • 8+ years of pharmaceutical experience, preferably in a global Quality Assurance or a Clinical Development setting., • In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections., • 2+ years of experience in SOP writing essential. For additional information, and a confidential discussion, please apply now with an updated CV.

Building Services Engineering Data Centre - Shift Manager - £65,000-£70,000 + Facilities Engineering Contractor is a leading global provider of integrated facilities and real estate management services. We are seeking an experienced Shift Manager to lead our engineering team at a data centre in Slough. This role is responsible for supervising planned and reactive maintenance activities, ensuring compliance with site policies, health and safety standards, and regulatory requirements. The Shift Manager will also act as the site Authorised Person, managing all safety documentation and operational controls, while coordinating daily shift operations and technical leadership. Key Responsibilities • Oversee and coordinate all shift maintenance activities (planned/reactive) to meet SLAs, • Monitor Building Management Systems and respond to alarms/emergencies, • Implement and manage the Permit to Work system, ensuring vendor compliance, • Ensure SOPs/EOPs and switching schedules are aligned with safety procedures and company policy, • Maintain compliance of cooling and domestic water systems (L8), • Manage spare parts inventory and ensure availability for maintenance tasks, • Supervise subcontractors and ensure adherence to site protocols, • Promote a professional and safety-first environment, • Develop strong relationships with clients and stakeholders, • Provide technical leadership and guidance to the shift team, • Review and approve RAMS, and prepare comprehensive job packs, • Monitor team performance, conduct reviews, and support training and development, • Manage shift ROTA, including leave, sickness, and return-to-work processes, • Maintain site documentation, statutory log books, and vendor report records, • Lead on-site incident management and emergency response drills Qualifications & Skills • HV Authorisation (required), • NVQ Level 3 or equivalent in a relevant discipline, • Current Wiring Regulations certification, • Emergency First Aid at Work, • Manual Handling, PASMA & IPAF (preferred), • Proven experience in a critical environment and real-time fault management, • Strong knowledge of Health & Safety compliance in maintenance environments, • Experience working with complex systems (e.g., Fire, PMS, BMS), • Strong organisational and leadership skills, • Excellent communication, both written and verbal, • High level of integrity and accountability, • Able to work independently and as part of a team, • Physically fit and able to work at height, • Flexible with shift hours and operational demands

New Product Development Manager - Slough - Permanent My client, a market leader within their sector are looking to recruit a New Product Development Manager to join their organisation. The role can be described as follows: Purpose of the role: Lead the development of our products from concept through to production. This includes translating market and technical requirements into product specifications, coordinating with Product Management, and managing cross-functional New Product Introduction (NPI) activities across the business. Key responsibilities include: • Lead NPD projects from concept, specification, and prototyping through to detailed design and production release., • Collaborate with Product Management to validate customer needs, market demands, and regulatory standards., • Consolidate requirements from diverse markets including food & beverage, pharmaceutical, industrial, and municipal sectors, into structured, actionable product specifications., • Convert complex requirements into innovative UV system designs that balance performance, compliance, scalability, and cost-effectiveness., • Coordinate development and NPI efforts across Engineering, Product Management, Operations, and Commercial teams to ensure aligned execution and smooth product delivery., • Contribute to strategic planning and roadmap development for our products and services., • Manage technical documentation and ensure compliance with internal and external standards., • Champion continuous improvement in technical processes and tools., • Mentor and coach team members to support their professional growth. Candidate requirements: • Must have a relevant qualification, preferably a good degree, or suitable experience., • Experience leading New Product Development (NPD) from concept to launch., • Strong design and systems thinking, with the ability to convert complex, multi-market requirements into scalable, compliant, and cost-effective solutions., • Proven ability to influence cross-functional teams (Engineering, Product Management, Operations, Commercial) to align with product goals and drive execution., • Skilled in mentoring and developing technical talent., • Demonstrable experience to continuous improvement in tools, processes, and team performance., • An inquisitive hands-on approach with excellent problem-solving skills., • Be a self-starter with a results-driven can-do attitude with the ability to adapt to change., • Willing and able to be in our Slough offices 5 days a week If this exciting opportunity could be of interest - please let me know ASAP. Interviews can be arranged at short notice.

Job Title: Governance and Reporting Manager Location: Slough, Hybrid Contract: 3-month Hours: Full-time About Randstad Sourceright Randstad Sourceright is proud to partner with Mars, a global leader in food, pet care, and confectionery. Through our partnership, we connect talented professionals to exciting opportunities within Mars’ world-class operations. Position Overview We are seeking a highly motivated Governance and Reporting Manager to join the Pet Nutrition Europe Controllership Team at Mars. This role is ideal for a finance professional with strong accounting, reporting, and governance experience who thrives in a fast-paced, collaborative environment. You’ll play a key role in ensuring financial integrity, driving compliance, and supporting the implementation of governance frameworks across multiple markets. Key Responsibilities • Ensure accurate accounting and healthy balance sheets and P&Ls across markets within the Cluster, collaborating closely with MGSF and Reporting Analysts., • Deliver timely, complete, and compliant financial statements and reporting in line with Mars GAAP, US GAAP, and regulatory standards., • Oversee the implementation and execution of the internal controls framework, testing plans, and governance agenda., • Partner with Cluster Finance Directors, General Managers, and cross-functional teams to maintain a strong control environment., • Act as a champion for financial controls and governance, promoting a culture of trust, accountability, and collaboration across Finance and non-Finance teams., • Support the cascade of global policies and processes within the Cluster as part of Mars’ Controllership operating model Candidate Profile Essential Qualifications & Experience: • University degree (or equivalent), preferably in Accounting or Finance., • Strong accounting and finance background with a proven track record of delivering high-quality results., • Proficiency in SAP or equivalent ERP systems., • Knowledge of US GAAP, internal controls, and regulatory reporting requirements., • Digitally savvy, with a user-focused and problem-solving mindset. Core Competencies: • Action Oriented, • Communicates Effectively, • Decision Quality, • Ensures Accountability, • Instills Trust, • Manages Complexity, • Optimizes Work Processes Why Join? You’ll be joining Mars, a global organisation committed to quality, innovation, and sustainable growth. This is an exciting opportunity to contribute to a key transformation period, gain hands-on experience within a global finance environment, and develop your skills in a structured, professional, and collaborative culture.

Job Description: Job Level Descriptor: • Performs defined assignments in the entry level of the technical leadership career band, • Typically requires a college or university degree and has conceptual knowledge of theories, principles and practices, • Develops competence by performing structured work assignments, • Problems faced are difficult but typically not complex, uses existing procedures and practical knowledge to solve problems, • Works independently and receives instruction, guidance and direction with general supervision, • May influence others within the job area through explanation of facts, policies and practices Job Family Group: R&D Delivers value and growth by driving product quality, assuring consumer safety and promoting efficiency based on robust science while developing consumer-relevant products, process and packaging. Job Family: Packaging Design Roles which fuel the innovation pipeline (build, expand and disrupt core innovation), identifying and translating consumer, shopper and customer insights into key quality attributes (KQA) and desirable packaging taken from first prototype through to industrial production. Custodians of brand technical knowledge and accountable for ensuring KQA are set and maintained during change projects (raws, process or continuous improvement). Packaging Design Engineering Packaging Design Engineering focuses on designing and developing product packaging (e.g., boxes, cartons, bottles, plastic wraps and other containers) including: -Designing and constructing new packaging or improvements to existing packaging; testing, analysing, and selecting materials for packaging based on durability and cost effectiveness -Supporting and participating in the design, test, modification, fabrication, and assembly of prototypes -Designing process(s) to manufacture packaging; overseeing the installation, operation, and maintenance of packaging machinery, systems, and processes to ensure optimal performance -Designing quality assurance/control processes and procedures into packaging design which may include compliance with specific technical and regulatory standards related to product packaging

This is an exciting opportunity to join a respected Employment Law team based in Eton. The role offers a competitive salary of £50,000+ (DOE), excellent progression opportunities, and an outstanding benefits package — including generous leave, life insurance, and flexible hybrid working (just 1–2 days per week in the office for the right candidate). About the Firm: My client is a well-established law firm with a strong reputation in claimant employment law, acting for both private individuals and trade union members. The firm values professionalism, empathy, and collaboration, offering a supportive environment where career growth and work-life balance are genuinely encouraged. Employment Solicitor — Position Overview: • Manage your own varied employment law caseload, • Act for claimants in both litigated and non-litigated matters, • Handle settlement agreements and negotiate favourable outcomes, • Provide legal advice to union officers through the firm’s advice line, • Support Partners and Senior Solicitors on complex, high-value matters, • Maintain compliance with procedural and regulatory standards, • Manage financial aspects of files (WIP, disbursements, billing, and profitability), • Deliver excellent client care and timely communication throughout each case, • Contribute to firm-wide business objectives and team growth Requirements of the Employment Solicitor: • Qualified Solicitor with a valid, clean Practising Certificate, • NQ+ PQE in Employment Law (claimant experience preferred), • Strong academic background and technical knowledge of employment litigation, • Excellent communication and client care skills, • Professional, empathetic, and solution-focused approach, • Strong organisation, time management, and problem-solving abilities, • Confident user of Microsoft Office and case management systems, • Commercial awareness and commitment to service excellence The Benefits for the Employment Solicitor role: • Salary from £50,000+ (DOE), • 20 days’ annual leave rising to 25 after probation, • Birthday leave — never work on your birthday, • Full paid Christmas closure (25 Dec – 1 Jan) in addition to annual leave, • Life insurance (2x salary), • Health cash plan, 24/7 GP access & online health assessments, • Perks & discounts app (shopping, lifestyle, wellbeing), • Gym discounts & digital fitness subscriptions, • Employee Assistance Programme with counselling & mental health support, • Paid professional memberships (APIL / CIPD / AVMA), • SRA practising certificate fully funded, • Enhanced maternity & paternity pay (top-up to 100% for 3 months where eligible), • Agile working policy — 1–2 days per week in the office for the right candidate, • Recognition for work anniversaries and achievements If you’re an Employment Solicitor ready to take the next step in your career, apply today. Alternatively, contact Shabir at Law Staff Limited quoting reference BH-37441 PLEASE CHECK YOUR EMAIL (INCLUDING SPAM FOLDER) FOR CONFIRMATION THAT YOUR APPLICATION HAS BEEN RECEIVED. In accordance with The Conduct of Employment Agencies and Employment Businesses Regulations 2003

As Compliance Manager, you'll oversee and drive compliance across key areas including:. Our client is committed to safety, integrity, and service excellence-and they're now seeking a Compliance professional who shares those values and can lead across a wide range of statutory and regulatory obligati

Hobson Prior is seeking a Pharmacovigilance Manager to join a pharmaceutical organization based in London. In this role, you will focus on ensuring the safety of medicines and compliance with regulatory requirements. This is an excellent opportunity for someone passionate about drug safety and patient well-being. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: • Oversee and manage drug safety processes to ensure compliance with regulations., • Monitor and evaluate the safety of medicines, identifying and addressing any risks., • Prepare and review safety reports and documentation., • Collaborate with internal teams and external partners to maintain high safety standards., • Ensure timely reporting of safety information to regulatory authorities. Key Skills and Requirements: • Strong understanding of pharmacovigilance principles and regulations., • Ability to analyze and interpret safety data effectively., • Excellent communication and organizational skills., • Experience in managing safety processes and working with cross-functional teams., • Proficiency in relevant software and tools used in pharmacovigilance. For more information, please contact William Tyler. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - .

Job Title: International Regulatory Affairs Advertising and Promotion Area Lead An exciting opportunity has arisen for a dynamic and driven regulatory professional to join in this leadership role. This high-impact position will ensure that all promotional and non-promotional materials are accurate, balanced, and compliant with applicable industry codes, internal policies, and local regulations. As Area Lead, you will provide expert guidance on promotional compliance and act as a strategic partner across functions, contributing to key business decisions and driving operational excellence in a matrixed, fast-paced environment. Key Responsibilities: • Leading a UK-based team (with potential to support additional affiliate teams) focused on the review of promotional and non-promotional materials., • Helping ensure materials meet local regulatory requirements and industry Codes of Practice, while still supporting creative and commercially relevant messaging., • Working closely with international colleagues to align campaigns and review processes between global and local teams., • Offering practical guidance and regulatory insight to colleagues across different teams, including Commercial, Medical, Legal, and Compliance., • Staying up to date with relevant regulatory changes and helping teams understand their impact., • Bringing a thoughtful, balanced approach to problem-solving, supporting both compliance and business needs., • Supporting ongoing process improvements and contributing to broader regulatory and business strategies., • Creating a positive, inclusive team environment that supports development and growth. Qualifications & Experience: • A Life sciences degree, • UK-registered Medical Signatory status, • Experience working in the pharmaceutical industry, • Some leadership or team management experience, with a supportive and coaching-led approach, • Confidence working across different teams or departments, especially in complex or matrixed organisations, • Comfortable supporting a wide range of products, including those at various lifecycle stages, • Clear and confident communication skills – both written and verbal, • A collaborative mindset and the ability to guide others through complex decisions Salary and benefits: A highly competitive salary, car allowance, annual bonus, private healthcare and wider benefits are on offer To apply for this position or hear further details then please click “Apply” or reach out via email –

Job Title: Real World Evidence (RWE) Coordinator Location: Maidenhead (Hybrid – 3 days onsite) Contract: 12-month Fixed Term Contract Are you an organised, detail-oriented individual with a passion for clinical research and real-world evidence? We are looking for a Real World Evidence Coordinator to join our UK Medical Operations team on a 12-month contract. About the Role As the RWE Coordinator, you’ll play a key role in the coordination and compliance of investigator-initiated and affiliate-driven research. Acting as a Subject Matter Expert (SME), you’ll support clinical study setup, manage TMF documentation, oversee drug supply logistics, and ensure financial and regulatory compliance throughout the study lifecycle. Key Responsibilities • Act as SME for set-up processes in investigator-initiated studies, • Support study feasibility, tracking, and delivery of investigational product, • Maintain TMF/eTMF for clinical studies, • Partner with Medical Operations and external collaborators, • Manage study budgets, contracts, and invoice tracking, • Ensure audit and inspection readiness, • Identify process improvements and efficiency opportunities What We're Looking For • Degree in Life Sciences (e.g. Pharmacy) or relevant experience, • Prior experience in clinical research operations, • Strong understanding of GCP, ICH Guidelines, and UK regulations, • Proven TMF management and investigational drug shipment experience, • Contract and finance experience desirable, • Excellent Excel and IT skills, • Highly organised, proactive, and a great communicator Why Join Us? You’ll be part of a collaborative, high-performing team working on meaningful research that drives real-world impact for patients. We offer a supportive hybrid work environment, opportunities for professional growth, and a chance to contribute to exciting studies.

Health and safety manager Film, TV & events | Farnham Royal About Palmbrokers Palmbrokers is a leading greens company supplying, making and dressing natural scenery and props for film, television and events across the UK and internationally. The company was established in 1986 and operates from a 25+ acre site in Farnham Royal, Berkshire. Palmbrokers is a fast-paced, vibrant and exciting place to work where the team always finds a way for clients, no matter the request. About the role Palmbrokers’ health and safety system exists to keep people safe within that client-led culture of creativity. Excellent and instinctive communication is key for the health and safety manager to foster understanding and a strong sense of responsibility for safety within every individual. Every member of staff must be sufficiently trained and aware that their health and safety responsibilities are a critical and integral part of what they do. What you’ll do As Palmbrokers’ health and safety manager, you will work across the business to lead and drive all aspects of health and safety, facilitating a culture of safety and continuous improvement as well as providing assurance to the Board of Directors that Palmbrokers complies with relevant legislative requirements and accepted industry guidance. • Lead the implementation and monitoring of the health & safety management system, ensuring compliance with UK legislation including the Health and Safety at Work Act 1974., • Oversee health and safety across two premises, transport operations and off-site working environments including film and TV production locations, live event venues and international projects., • Continually assess risks across all areas of the business, prepare and review risk assessments and method statements, and work closely with staff to create and embed safe systems of work., • Ensure safety in key risk areas including manual handling, loading and unloading large containers, vehicle operations and working in unfamiliar environments., • Deliver inductions, toolbox talks and refresher training; maintain a training needs analysis and a full training matrix to build and track competence across the workforce., • Establish audit processes, undertake inspections and site visits, lead on formal accreditations, and liaise with regulators, insurers, clients and other external bodies., • Maintain and analyse records of incidents, accidents and near misses; lead investigations and corrective actions., • Engage with employees and contractors, consult with safety champions and develop worker participation in a positive safety culture., • Develop and test emergency response procedures for both on-site and off-site environments, ensuring first aid provision and incident management is robust. What we’re looking for • Essential: NEBOSH General Certificate (or equivalent), strong knowledge of UK H&S legislation and management systems (e.g. ISO 45001), full UK driving licence., • Desirable: NEBOSH Diploma, IOSH accreditation (Technical or higher), Fire Risk Assessor qualification, CITB SMSTS or NEBOSH Construction., • At least 5 years’ experience in a senior health and safety management role with responsibility for risk assessments, training, compliance and procedure development., • Strong organisational and analytical skills with the ability to develop solutions and advise senior management on emerging risks and regulatory changes., • Excellent communication and interpersonal skills; able to influence at all levels, motivate staff and build effective working relationships internally and with clients., • Experience in logistics, horticulture, plant hire, events or production environments is an advantage. What we offer • A unique and challenging role that blends structure with variety across creative, horticultural and production sectors., • Opportunities to support high-profile productions and events in the UK and overseas., • Investment in your professional development and industry-specific training., • A collaborative, fast-moving and highly creative workplace where health and safety is an essential and integral part of the business. Palmbrokers is proud to be an equal opportunities employer. We value and celebrate diversity and we are committed to creating an inclusive environment for all employees. We welcome applications from people of all backgrounds, cultures and experiences and we ensure that every member of our team feels respected, supported and able to contribute fully.

Compliance Manager Property Services – FRA, M&E & Gas Up to £60,000 Plus Package Our client, a growing construction contractor who operate nationally, are looking to add an experienced Compliance Manager to one of their long term frameworks in Berkshire. They provide R&M, planned maintenance, FRA and compliance solutiosn to local authorities and housing associations across the UK. Within this particular role, you would be responsible for the compliance workstreams which will include Fire Safety, M&E, Legionella & Gas. Accountabilities/Responsibilities: • Lead the development, implementation, and monitoring of compliance policies and procedures across the housing stock., • Ensure compliance with statutory obligations, including Health & Safety at Work Act, Building Safety Act, Housing Health and Safety Rating System (HHSRS), and all relevant sector-specific regulations., • Oversee regular audits and inspections, ensuring that all remedial actions are recorded, tracked, and completed in a timely manner., • Manage contracts and performance of external contractors delivering compliance-related services (e.g. gas servicing, fire risk assessments)., • Maintain accurate compliance records and provide regular reports to senior management, the board, and regulatory bodies., • Work with asset management, repairs, and housing teams to embed a compliance-focused culture., • Act as the main point of contact for regulators such as the Regulator of Social Housing and the Health and Safety Executive (HSE)., • Lead on internal investigations and reporting for incidents related to non-compliance or safety breaches., • Manage and develop a team of compliance officers or coordinators, where applicable. Skills & Experience: • Proven experience in a compliance, health & safety, or asset management role within the social housing or property management sector., • Detailed knowledge of relevant housing and building safety legislation and best practice., • Strong project management and contractor management skills., • Excellent analytical and reporting abilities., • Experience in policy development and audit processes. Having an ability to create a strong working environment, where everyone is working as a team to achieve targets and goals on the contract, as well as being able to build strong relationships with the client and your team members. This is an excellent opportunity to join an established and reputable business. My client are offering an excellent salary & package and benefits. If this role is of interest please apply or contact Danny Mangan. Fortus Recruitment Group Limited acts as an Employment Business for the supply of temporary workers and an Employment Agency in relation to permanent vacancies. Fortus Recruitment Group is an equal opportunities employer

! Location: Slough, and likely fully onsite Start date: ASAP Type of position: 12 months contract (Has to the view to be extended) Job Description Partnered with a global leader in multinational company that provides contract development and manufacturing services (CDMO) to the pharmaceutical, biotechnology, and nutrition industries. They help companies bring new therapies to market by offering everything from early-stage research support to large-scale production. Overview: This is a hands-on, lab-based scientific role focused on driving innovation in bioprocess sciences. The position supports the development and optimization of purification processes to meet evolving industry needs through technical experimentation and data-driven solutions. Role Purpose: Contribute to the design, planning, and execution of studies that support technology development and process improvement. Conduct experiments within defined scopes and timelines, and analyze results to guide next steps in development. Key Responsibilities: • Support the interpretation of problem statements and study rationale to ensure alignment with project objectives, • Assist in developing and executing high-throughput (HTP) workflows for process studies under supervision, • Configure HTP equipment to enable reliable monitoring and data capture, • Identify potential risks to study execution and contribute to mitigation strategies, • Collaborate on study plans and documentation with senior team members, • Execute HTP studies according to protocols and timelines, and perform preliminary data analysis, • Contribute to improving HTP workflows for greater efficiency and integration into broader development pipelines, • Provide purification support during technology implementation in cross-functional settings Work Practices: • Deliver experimental support for bioprocessing technology development and implementation, • Maintain accurate records in accordance with quality standards and project requirements, • Perform technical analyses and assist in preparing reports and presentations, • Participate in team planning by updating task progress and resource needs, • Follow good laboratory practices and support equipment maintenance and housekeeping, • Adhere to safety, health, and environmental guidelines, including participation in risk assessments, • Ensure compliance with data integrity, documentation, and training standards 👤 Candidate Profile: • Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemical Engineering, or related life sciences, • Hands-on experience with high-throughput purification workflows, chromatography, and filtration techniques, • Familiarity with bioprocessing equipment, • Understanding of process development, scale-up, and tech transfer If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! About Planet Pharma Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

My client a mid-sized pharma company based in Berkshire is seeking a Local Safety Officer (LSO) who will be responsible for managing pharmacovigilance (PV) activities ensuring compliance with local and global PV regulations. 1 day per week based in the office Competitive salary, excellent benefits • Enter adverse event reports into safety databases (e.g. Argus / Global Intake Tool) under supervision, • Manage the local safety mailbox and process spontaneous safety reports from healthcare professionals, patients, and other sources, • Coordinate product quality complaints with the regional Quality team.Support signal detection activities and escalate local safety signals to global teams, • Respond to safety-related requests from regulatory authorities and patient associations., • Conduct local literature screening for safety-relevant information not covered in global searches, • Review and maintain local SOPs and contribute to global SOP reviews impacting PV., • Oversee aggregate reports (PSURs, DSURs), safety variations, and Risk Management Plans (RMPs), • Collaborate cross-functionally with medical, regulatory, quality, clinical, and commercial teams, • Participate in audits, inspections, and ensure CAPAs are implemented effectively, • Deliver basic PV training to new staff and external service providers, • Ensure continuity of local PV activities, including out-of-hours coverage and business continuity planning. Qualifications & Skills • Graduate science degree in health / life sciences, • Minimum of 3 years PV experience, • Good knowledge of Pharmacovigilance legislation where appropriate., • Practical experience in process development and improvement activities that embed quality and drive continuous improvement., • Experience in process mapping and writing process documents., • Flexible approach, readily adapting to changing circumstances and new opportunities; encourages, leads, facilitates and drives change where appropriate., • Challenges and questions ways of working to seek improved processes., • Excellent attention to detail.

Senior Regulatory Affairs Manager – Europe Slough – Hybrid. Full time, Permanent This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. The role involves strategic input into development programs, preparation and submission of regulatory documentation, and post-approval lifecycle management. You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: • Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions., • Review non-clinical and clinical data packages for regulatory adequacy and compliance., • Conduct due diligence across CTD Modules 1–5 and review sections of Marketing Authorisation Applications (MAAs)., • Coordinate registration and maintenance of assigned generic products., • Support regulatory authority interactions, including scientific advice procedures., • Maintain regulatory databases and document management systems., • Guide junior staff and contribute to process improvements within the regulatory function., • Ensure alignment with EU regulatory requirements for product launch and lifecycle activities. Required Experience & Qualifications: • Strong, clear evidenced experience with European regulatory frameworks and submission pathways (DCP, MRP, national procedures)., • Proven experience in regulatory strategy development for specialty and generic products- minimum 7 years industry experience, • Hands-on experience with post-approval activities, variation strategies, line extensions and due diligence ., • Familiarity with regulatory tools and platforms (eCTD, CESP, MHRA portal, Eudralink)., • Ability to critically evaluate scientific data and identify regulatory risks and mitigation strategies., • Degree or higher qualification in Pharmacy, Life Sciences, or a related field., • Excellent communication, project management, and cross-functional collaboration skills., • Experience managing regulatory timelines and approvals in a fast-paced environment. All applicants must hold valid right to work as sponsorship is unavailable. Must be located within a commutable distance to SL1 and comfortable working from the office at least 3 times per week.

You will be responsible for providing comprehensive administrative support across commercial and compliance activities, ensuring smooth processes and adherence to regulatory requirements. A key aspect of this position is handling day-to-day administrative tasks such as data entry, scheduling, and fo

Manage contracts and performance of external contractors delivering compliance-related services (e. Maintain accurate compliance records and provide regular reports to senior management, the board, and regulatory bodies. Our client, a growing construction contractor who operate nationally, are looki

The Financial Accounting Manager, based in Maidenhead, will lead financial reporting and ensure compliance across a global healthcare organisation, requiring strong expertise in internal audit, accounting, and regulatory standards. Lead statutory accounting processes, including audit planning and go

You will be responsible for responding to and processing all customer/dealer enquiries through the provision and collation of timely and accurate information and the completion of all relevant transactions.Through day to day actions ensure compliance of all regulatory requirements and industry stand

Position: Insights Governance Administrator - Market Access Location: Slough, UK - Hybrid Client: Global Leading Biotechnology Type: 12 months Contract Planet Pharma are we are partnered with a Global Leading Biotechnology company, who are currently hiring for an Insights Governance Administrator within Market Access teams. Main Responsibilities include: • Provide expert support and troubleshooting for stakeholders using the Market Research System and ensure alignment with Standard Operating Procedures (SOPs)., • Triage and respond to governance-related queries submitted via the MR Governance mailbox., • Engage with Insight Leads and Managers to understand their governance needs, sharing insights and identifying opportunities for process improvement., • Conduct periodic and ad hoc reviews to verify the accuracy and timeliness of compliance documentation., • Collaborate with Insights Governance team members to maintain and enhance governance standards and processes. Main Requirements: • Bachelor’s degree required., • Proven experience managing multiple projects, with strong organizational and vendor management skills., • Strong operational mindset with a proactive approach to identifying and solving issues., • Excellent collaboration and communication skills; comfortable working with stakeholders across functions and levels., • Detail-oriented with a structured, logical approach to problem-solving and a strong compliance focus. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

As Compliance Manager, you'll oversee and drive compliance across key areas including:. Our client is committed to safety, integrity, and service excellence-and they're now seeking a Compliance professional who shares those values and can lead across a wide range of statutory and regulatory obligati

Process Safety Consultant ( Regulatory / Compliance / COMAH )Remote with travelChemical Manufacturing/ Manufacturing / Process Plant / Refinery / Petrochemical / Oil&Gas / LNG LPG Ammonia<

The position is responsible for compliance activities such as advising on evolving regulatory developments, enabling market access, reporting compliance trends, managing first-party product investigations and recalls, managing third-party recalls, and auditing product compliance on the SHEIN Marketp

This role is pivotal in ensuring compliance with European regulatory requirements, developing and implementing regulatory strategies and continued portfolio expansion via acquisition. Significant (Minimum 8 years) experience managing lifecycle regulatory activities for established products in Regula

Location: Remote UK residents only Start Date: 26th January 2026 Working Hours: Monday to Friday, 09:00 17:30 Salary: £25,000 per annum Benefits: 25 days holiday plus a fantastic range of benefits For over 25 years, Kensington Mortgages has been a leader in specialist mortgage solutions. We're committed to helping people secure mortgages when traditional lenders say no that's the Kensington Difference . As a wholly owned subsidiary of Barclays Bank UK PLC, we operate with integrity and excellence, fully authorised by the Financial Conduct Authority. As a Customer Service Agent , you'll be the voice of Kensington Mortgage Company (KMC), supporting customers over the phone with queries, complaints, and general mortgage assistance. From account opening to closure, you'll ensure every customer receives outstanding service. You'll handle a wide range of enquiries from payments and balances to redemptions making a real difference in our customers' lives. • Respond to inbound customer queries on topics such as payments, balances, interest rates, account updates, and terms., • Update customer records and process account changes accurately., • Investigate and resolve internal and external requests efficiently., • Prioritise workloads in line with service standards., • Ensure compliance with policies, procedures, and regulations., • Assess risk factors during daily tasks., • Identify opportunities for process improvements., • Maintain strict adherence to regulatory and policy requirements., • Experience in a telephony-based role within a regulated environment (financial services/mortgages preferred)., • Proven ability in a target-driven, customer-focused setting., • Excellent verbal and written communication skills., • Empathy and the ability to support vulnerable customers., • Strong problem-solving and objection-handling skills., • Confidence using Microsoft Office and navigating multiple systems while on calls., • A positive attitude towards change and adaptability. We are proud to be an equal opportunity employer, embracing differences in gender, race, identity, ethnicity, and sexual expression. If you're passionate about delivering exceptional customer service and want to be part of a team that values your contribution we'd love to hear from you. Apply today and become part of the Kensington Mortgages family, helping us continue to make a positive impact in our customers' lives. • We're looking for candidates who can start remotely on Monday 26th January 2026, • To get the most from our training, please avoid taking annual leave during the first 7 weeks ., • All offers are subject to background checks, including DBS, credit, and Right to Work., • To use our digital Right to Work checks, you'll need a valid passport. Otherwise, you'll need to visit our Marlow, Buckinghamshire office to present ID.

This is a high-impact leadership role focused on the financial oversight and regulatory compliance of our Funeral Plan Trusts. Lead all financial oversight and regulatory compliance for Dignity's. Own financial strategy, investment oversight, risk mitigation, and FCA submissions; collaborate with in

As this role is UK based, support, guidance and training will be provided to help the Compliance Executive – Financial Promotions to understand regulatory requirements in markets outside of the UK. Demonstrable, relevant experience in a Compliance role within financial services, with strong experi

Health & Safety Compliance Assessor (Part-Time) – on-site role located in Berkshire / Oxfordshire / Hampshire. This part-time on-site role involves conducting health and safety audits, ensuring regulatory compliance, performing risk assessments, documenting findings, and delivering training sessio

Our client is committed to safety, integrity, and service excellence—and they're now seeking a Compliance professional who shares those values and can lead across a wide range of statutory and regulatory obligations.As Compliance Manager, you'll oversee and drive compliance across key areas includ

This is a role with real influence! Required Knowledge & Experience - Strong background in Remediation & Regulatory Compliance within Financial Services Proven experience as a senior leader with the ability to influence at the highest levels, balancing strategic vision with operational delivery U

The corporate Safety manager responsible for developing and maintaining all relevant Technical Safety engineering strategies, policies and procedures necessary to ensure regulatory compliance, safe and efficient operation of Petrofac operated assets, supported assets and contracts. Extensive knowled

This is a role with real influence! Required Knowledge & Experience - Strong background in Remediation & Regulatory Compliance within Financial Services Proven experience as a senior leader with the ability to influence at the highest levels, balancing strategic vision with operational delivery U

Experience working in a compliance-focused role within a defence, aerospace, or highly regulated engineering environment. Regulatory & Export Control Manager. Reporting to the GM, you'll lead the development and oversight of export compliance and legal governance across multiple UK manufacturing and

We're looking for a Wealth & Trading Regulatory Compliance Manager with expertise in EMIR and MiFID to lead the implementation of the regulatory framework around derivatives. Working with global Regulatory Compliance Managers to ensure that local risk management frameworks and processes are aligned

We are seeking a Product Compliance & Regulatory Affairs Specialist to ensure our kids’ consumer electronics meet all relevant international safety and regulatory standards. This role will manage compliance labelling, product certifications, regulatory product testing, and technical documentation

Regulatory Compliance Programme Manager. Regulatory Compliance Programme Manager -. Director of Regulatory Compliance.

Create realistic situations involving regulatory investigations, audit procedures, policy interpretation, enforcement actions, and compliance assessments. Regulatory Compliance Specialist. Regulatory Compliance Specialist.

Regulatory and Export Compliance Manager. Acting as the primary liaison for HMRC, including audit preparation and regulatory inspections. Introducing standardised filing procedures and export compliance packs across all UK sites to ensure audit-readiness and operational consistency.

The team has a broad economic crime practice with expertise in Enforcement, Internal Investigations, Compliance, and Crisis Response. The team provides advisory services on economic crime compliance, investigation and defence of clients across all sectors that DWF operates in. Maintain an understand

Regulatory Compliance Specialist - Remote | Upto $100/hr Remote. Regulatory Compliance Specialist - Remote | Upto $100/hr Remote. Create realistic situations involving regulatory investigations, audit procedures, policy interpretation, enforcement actions, and compliance assessments.

Lead the compliance and regulatory affairs function as the business transitions from payments (EMI) to investment services under MiFID II. Strategic insight — but also hands‑on expertise to shape, document, and deliver regulatory compliance. We’re looking for a Compliance Director who can take

Housing Regulatory Compliance Officer. Join Us as a Housing Regulatory Compliance Officer. Housing Regulatory Compliance Officer.