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Network Engineer Hybrid (2 days a week) Contract (6+ Months) Inside IR35 Canary Wharf, UK Knowledge, skills, and abilities • A solid network/security/cloud engineer with a strong focus on cloud hosted environments within AWS and Azure as well as excellent skills in firewall deployment, routing and switching., • In-depth knowledge of design, implementation, configuration and testing of the following:, • Routing – OSPF, BGP, knowledge of route redistribution and manipulation., • WAN - MPLS, Internet, VPN, SDWAN, understanding of circuit commissioning., • Datacenter – ACI spine and leaf, APIC, VxLAN and distribution switching., • Encryption - IPsec VPN, MACSec, configuring site-to-site VPN on routers and firewalls., • Switching and L3 - HSRP, VRRP, GBLP, NTP, STP, RSTP, QoS, CoS, SVI, VLAN’s, ACL’s., • WiFi – Cisco Meraki and Cisco Wireless LAN controllers with Lightweight APs., • Firewalls – Cisco ASA/FirePOWER, Conversion from ASA code to Firepower, Checkpoint, Fortigate, ACL’s, CSM/FMC. Job purpose • Provide last line support for solutions delivered by the engineering function in line with existing IT service management processes. Act as an escalation point, for the managed service, for problems pertaining to network technology and with a view to re-engineering., • Perform all changes to organisation standards across the whole network stack, including cloud, on-premises datacenters, including internet edge and ACI Fabric, branch, WAN, and operate CSM/FMC to deploy firewall rules where required., • To design and implement network connectivity between on premise datacenters and the cloud and within the cloud. This will require an extensive knowledge of Direct Connect, leveraged through Equinix Fabric and familiar with AWS DX gateways, AWS Transit Gateways (TGW) and site-to-site VPN, to connect other third parties into the cloud and the on-premises networks to the cloud. A thorough understanding of VPC and VPC peering is essential., • Through knowledge of products across the AWS Market Place and familiar with setting up Cloud Services Routers (CSR’s) and firewalls from multiple vendors. These firewalls could be dual stack with separate vendors with HA being essential. This may extend to Autoscaling. Experience of AWS Firewall is preferred., • Knowledge of IPS at all layers across the firewalls is required along with an understanding of FirePOWER services., • Experience of implementing ExpressRoute within a hybrid Exchange environment, using a combination of on-premises servers and M365 SaaS., • Comfortable with firewall platforms such as Cisco ASA/FirePOWER, CheckPoint, multiple context firewalls from Cisco and CheckPoint and the tools used to deploy the rules such as Cisco CSM (Cisco Security Manager), Cisco FMC (FirePOWER Management Centre), Fortigate/Fortinet etc., • Strong debugging skills are required with the ability to run packet captures and wireshark traces. Good working knowledge of ACL’s., • Good understanding of BGP and OSPF along with policy-based routing and prefixes lists. This routing knowledge should be across ASR/ISR and IOS-XE., • A good understanding of NX-OS is required and any knowledge of ACI is preferred. Python and Postman is a bonus., • Datacenter switching and routing comprises Cisco ACI Fabric with a spine and leaf topology. The engineer should be familiar with operation of ACI deployed within the core infrastructure. The datacenter also features firewalling between Tenants, such as Production, Secure Management and Dev/Test., • Partners and vendors are connected via a separate VRF on the WAN and the webhosting environment features three tiered stacks (Cisco ASA, CheckPoint, Cisco ASA). Throughout this architecture, there are many DMZ’s so there should be a thorough understanding of all these technologies., • The engineer will also need to have a good knowledge of the tools used within the network, such as CMC for Riverbed, CSM for Cisco ASA, Voyager and CheckPoint Manager for CheckPoint, CPI for WiFi, ISE for NAC and future deployment of technology, such as TrustSec, RSA tools, Solarwinds Orion, Cisco ACS and Infoblox etc. A strong knowledge of WireShark is also required. Qualifications / certifications: · Engineering/Computer Science Degree or industry related qualifications, such as AWS and Cisco Certifications.

CMC Partners, part of the G&E Group, is a specialist Executive Search and Consulting firm working across the Construction, Engineering and Finance industries. We partner with some of the most respected organisations in the US, helping them identify and secure the leaders who shape the future of their sectors. We are now looking for ambitious graduates (2025/2026 year of graduation) to join our growing team as Executive Search Consultants, where you’ll gain the skills, training, and experience to build a successful career in executive search and talent consulting. The Role As a Consultant, you’ll play a key role in delivering high-impact recruitment and advisory projects. You will: • Work closely with clients to understand their business objectives and talent strategies, • Research, identify, and engage with senior-level professionals across specialist markets, • Conduct interviews and assessments to match candidates with the right opportunities, • Manage recruitment processes end-to-end, from initial briefing to offer negotiation and placement, • Build lasting relationships with clients and candidates while developing your own sector expertise This is a commercially focused, people-driven role offering exposure to senior decision-makers and complex business challenges from the outset. Training and Development Your professional development is at the core of what we do. At CMC Partners, you’ll benefit from: • Structured graduate training programmes designed to build your consulting, research, and communication skills, • Ongoing mentorship and coaching from experienced consultants and industry leaders, • Access to the G&E Academy, a tailored training programme supporting your long-term growth and professional excellence with our expert Learning & Development team We’re seeking graduates who demonstrate: • Strong commercial awareness and analytical thinking, • Confidence and clarity in communication, • Motivation to succeed in a performance-driven environment, • Resilience, adaptability, and a proactive mindset, • Curiosity about how businesses operate and what drives success Previous experience in client-facing, research, or sales-related roles is beneficial but not essential. Why CMC? • We offer one of the best commission structures in the industry, paying up to 60% of your fees. Our top consultants earn up to £80,000 in a single month!, • Exciting Incentives: From Michelin Star dinners to adrenaline-packed team activities like go-karting and paintball, we reward hard work. Our past quarterly incentives have included trips to Ibiza, Barcelona, Las Vegas, Meribel and even Sardinia!, • Young, driven company culture: Our people are our biggest pride! Aside from regular socialising opportunities, we genuinely aim to create a supportive and collaborative culture while driving growth from within. This is your chance to launch a high-earning, high-impact career — with real growth, real rewards, and real responsibility from the start.

We are seeking a Regulatory Affairs Manager to join our global team based in Hampshire, UK. The Regulatory Affairs Manager role offers you an exciting opportunity to join our highly motivated Product Development – Injectables team, a patient-centric, fast paced environment focused on rare diseases. This position operates within Alimera Sciences Limited, a subsidiary of ANI Pharmaceuticals, with a 3 day per week in office expectation. If you are a regulatory professional with European experience who is looking to expand and grow in their career, then this could be an excellent opportunity for your development! It is a global role, with a primary focus on our international (non-US) markets, which will provide opportunity for you to expand your international and US regulatory experience across a wide breadth of projects and submissions. The successful candidate will be responsible for leading regulatory activities for international projects, providing regulatory guidance and liaising with external partners including regulatory authorities. This role is a key member of a highly visible team and provides prominent exposure across multiple business units and with leadership. As a dynamic growing company, this role values accountability, adaptability and a proactive mindset to support the company’s expansion. TASKS / RESPONSIBILITIES • End to end management of complex global projects and submissions, from developing strategies through to the filing of applications and post-approval implementation., • Oversee and support licensing partners in international regions (including Middle East, Asia, Australia)., • Responsible for a range of submissions from initial authorisation applications, variations/supplements, annual reports through to clinical trials and educational materials., • Regulatory point of contact for key projects, collaborating closely with multiple cross-functional areas including PV, Quality, Manufacturing, Supply, Medical and Marketing., • Understand, interpret and advise on regulatory legislation and guidance., • Interact with regulatory authorities to facilitate successful submissions and approvals., • Author high quality Common Technical Dossier (CTD) modules and regulatory technical documents., • Input into cross-functional submission documents, e.g. clinical protocols, PSUR, DSUR, PADER, educational materials, quality/manufacturing reports., • Management of regulatory labelling texts, including coordination of translations. PROFESSIONAL QUALIFICATIONS/EXPERIENCE • Degree in life sciences, engineering, pharmacy or higher, • Minimum of 5 years experience in European Medicinal Regulatory Affairs., • Proven ability to accurately assess regulatory impact, develop effective strategies and deliver submissions. Prior experience with European MRP/DCP is required., • Excellent written and verbal communication skills in English., • Experienced at authoring regulatory technical and submission documents., • Proven track record with navigating post-approval CMC changes, including ability to identify regulatory impact, data requirements and achieve successful filings., • Sound performer in interacting with and influencing regulatory authorities., • Prior US medicinal regulatory affairs experience and familiarity with global regulations, including US, is beneficial but not required. Knowledge of medical devices and drug-led combination products is desirable. SKILLS AND COMPETENCIES • Effective and influential communicator – you have strong verbal and written skills, able to clearly convey regulatory positions and persuade internal and external stakeholders., • Broad knowledge of European regulatory systems, including relevant current and upcoming legislation, • You can understand and interpret regulatory legislation and guidance documents., • Self-motivated, self-reliant and able to work independently in a fast-paced, deadline driven environment., • Effective networker and team worker – you are able to build effective working relationships with colleagues, external partners and regulatory authorities., • Strong analytical thinking and problem-solving skills, with a high attention to detail. Proven ability to deliver well thought-through and evaluated solutions., • Sound project management and organizational skills – you are able to effectively plan time and prioritize to achieve goals., • Flexible approach – able and eager to learn new things, think creatively and laterally, and think outside the box. Willingness to roll up your sleeves and get things done.

Automated Formulation Scientist London, UK On-site (with flexibility for hybrid working) We’re partnered with an early-stage platform biotech startup emerging from stealth, backed by leading venture capital investors. The company is building AI-driven “self-driving laboratories” designed to transform how drug products are developed. Their platform combines robotics, automation, and machine learning to explore vast formulation spaces, automatically design and run experiments, and continuously learn from the results. By replacing traditional trial-and-error experimentation with high-throughput automated workflows, they aim to reduce formulation development timelines from months to days while unlocking medicines that were previously too complex to develop. Operating at the intersection of biotech, robotics, and AI, the team is building the next generation of laboratory infrastructure to accelerate pharmaceutical innovation. This is a rare opportunity to shape how an AI-powered formulation platform is applied to real drug development challenges. You will be a scientific anchor: defining what gets tested, how it gets measured, and what the results mean, in close partnership with data scientists and automation engineers. Responsibilities • Design and execute formulation studies for biologics (mAbs, proteins, peptides+)., • Pioneer new formulation development technologies., • Define experimental conditions for optimisation, framing scientific problems so their ML platform can learn from them effectively., • Develop and apply analytical methods to assess critical quality attributes., • Develop new accelerated characterisation methods suited to high-throughput screening., • Design protocols for biologic formulation automation, with a focus on robustness and traceability., • Work with their Automation team to scale methods onto robotic platforms and with Engineering to ensure data is captured cleanly and in structured formats. Requirements • Advanced degree PhD/ MSc with industry experience in pharmaceutics, biopharmaceutics, or formulation science, with a focus on biologics., • Hands-on experience with excipient selection, protein stability mechanisms, and formulation assessment for biologics., • Practical command of characterisation techniques., • Comfortable interpreting analytical data and making formulation decisions at startup pace, balancing scientific rigour with speed., • Clear communicator who can work across scientific and engineering disciplines. Desirable • Experience with high-throughput experimentation or automated liquid handling platforms (e.g., Hamilton, Tecan, Opentrons)., • Python or scripting skills for data analysis and visualisation., • Experience working with or developing ML models., • Familiarity with robotic workflows or automation-friendly SOP design., • Background in early-phase drug product development or CMC. Benefits • Competitive base salary alongside a meaningful equity package, giving you the opportunity to share in the company’s long-term success., • The chance to have real autonomy and impact within an early-stage startup, helping shape both the scientific direction and the development of the platform., • Direct exposure to founders and the C-suite, with the opportunity to influence strategy and decision-making as the company scales., • A beautiful, collaborative lab and working space in the heart of Central London, designed to bring scientists, engineers, and data teams together., • Hybrid flexibility, balancing hands-on lab work with the ability to work remotely where appropriate. Interested? Apply and we will be in touch!

G&L have multiple positions available for Regulatory Affairs Manager. We are growing our teams on a global basis; there has never been a more exciting time to join us! Please note that we have vacancies in Barcelona, Belfast London and Mumbai. If you have the experience we require and can work in one of our offices, we want to hear from you! Do you want to help bring life-changing medicines to the world? Are you passionate about science, strategy, and regulatory excellence? As a CMC Regulatory Manager, you’ll play a key role in ensuring that high-quality medicines continue to reach patients safely and efficiently across global markets. You’ll sit at the intersection of science, manufacturing, and regulatory strategy, guiding post-approval activities and ensuring that every change to our products meets global regulatory standards. If you enjoy solving complex problems, working across teams, and translating technical data into clear regulatory strategies, this role is for you. What You’ll Be Doing 🚀 Lead Post-Approval Regulatory Strategies Develop and implement regulatory strategies for post-approval CMC activities, including: • Variations, • Renewals, • Market expansions, • Annual reports Your work ensures our products continue to meet global regulatory expectations throughout their lifecycle. 🔍 Evaluate Manufacturing and Quality Changes Review change controls and assess how manufacturing or quality updates impact regulatory filings. You’ll determine: • Regulatory classification of changes, • Submission requirements, • Global regulatory impact 📊 Review Critical Scientific Data Collaborate with quality and manufacturing teams to review key reports such as: • Process validation studies, • Stability studies, • Analytical method validation You’ll ensure all data supports regulatory submissions and meets compliance standards. 🤝 Collaborate Across Teams Work closely with colleagues across: • Manufacturing, • Supply Chain, • Quality Control, • Quality Assurance, • Global Regulatory teams Your coordination keeps submissions accurate, complete, and on schedule. ✍️ Shape Regulatory Submissions Draft and review CMC sections of regulatory documents, including: • Variation submissions, • Responses to health authority questions 🗂 Manage Regulatory Systems Oversee projects within Regulatory Information Management (RIM) systems, ensuring global submissions are tracked, maintained, and compliant. ⚠️ Anticipate and Manage Risk Identify potential regulatory challenges early and implement strategies to keep projects on track. What You Bring Experience • Experience in Regulatory Affairs within the pharmaceutical industry, • Strong background in CMC or technical regulatory documentation, • Experience preparing CMC sections of regulatory submissions or variations, • Experience in validation, quality assurance, or pharmaceutical production is highly valued Technical Knowledge • Strong understanding of CMC and post-approval regulatory requirements, • Knowledge of:, • Stability studies, • Process validation, • Analytical method validation, • Comparability studies, • Experience working with Biological products or vaccines is a mandatory requirement for this role. Skills That Make You Shine • Exceptional attention to detail, • Strong problem-solving ability, • Excellent project management skills, • Ability to collaborate with cross-functional global teams Languages • Fluency in English (written and spoken), • Additional language (French, Italian, or German) is a plus. ✨ Why This Role Matters Your work ensures that safe, effective medicines continue to reach patients around the world — even as products evolve and improve. In short: you help science move forward, compliantly. Please only apply for this role if you have demonstrable experience working with Biologics or Vaccines

Please note that the successful candidate can work from our offices in Belfast, Barcelona or London The Opportunity We’re looking for a highly organised and proactive Technical Project Manager to support global product submissions within a fast-paced pharmaceutical environment. This role sits at the intersection of Technical Development and Regulatory Affairs, ensuring critical documentation is delivered accurately and on time to meet accelerated filing timelines. If you thrive on complexity, enjoy cross-functional collaboration, and have experience in CMC or pharmaceutical manufacturing, this is a high-impact opportunity to drive global delivery excellence. What You’ll Be Doing • Own and manage a global tracking system for critical source documents, including timelines, ownership, and dependencies, • Provide a single source of truth for document status, progress, and risks, • Build dashboards and perform trend analysis to track delivery performance, • Identify critical paths, risks, and bottlenecks, and drive mitigation actions, • Lead day-to-day follow-up on high-priority deliverables to ensure deadlines are met, • Oversee document lifecycle processes (authoring, review, approval, version control), • Coordinate cross-functional teams across technical and regulatory functions, • Deliver clear and actionable reports and updates to stakeholders What Success Looks Like • Seamless coordination of document delivery across global teams, • Early identification and resolution of risks impacting submissions, • Improved efficiency in document review and approval cycles, • On-time delivery of high-quality regulatory submission packages What You Bring Essential • Experience in CMC, biochemistry, or pharmaceutical/vaccine manufacturing, • Strong understanding of regulatory submissions and dossier preparation, • Proven project management expertise, including planning, tracking, and reporting, • Excellent communication skills in English (written and verbal), • French language skills are highly desirable, • Experience with tools such as MS Project or Planisware, • Familiarity with document management systems (e.g. Veeva, Documentum), • Previous experience in a large global pharmaceutical environment Why Join • Work on high-impact, global regulatory projects, • Collaborate with cross-functional scientific and regulatory teams, • Gain exposure to end-to-end product lifecycle processes, • Be part of a fast-paced, delivery-focused environment where your work directly contributes to bringing products to market

Your new companyA growing and well-established insurance group based in London is seeking an experienced IBA Manager to take ownership of their client money and finance operations. This is an exciting opportunity to join a forward-thinking business with strong leadership, a supportive culture, and a focus on continual improvement. Your new role In this role, you will be responsible for managing all finance and client money activities across the group, including: • Ownership and oversight of Client Money Calculations (CMC), • Ensuring compliance with FCA CASS rules and internal client money procedures, • Managing and reconciling client money accounts across multiple currencies, • Overseeing cash allocation, insurer settlements and aged balances, • Daily use and control of Xero and Global systems, ensuring accuracy and integrity, • Investigating and resolving discrepancies across systems and bank accounts, • Supporting RMAR reporting and other regulatory returns, • Maintaining strong financial controls and audit-ready processes, • Line-managing and developing the Accounts Assistant and wider finance team, • Collaborating with compliance and senior business units, • Identifying and implementing process improvements

Senior Technical Writer – CMC (Consultant) An experienced CMC Technical Writer is required to support late-stage drug development programmes, working on complex submission documentation within a fast‑paced development environment. What we’re looking for: • An established Regulatory CMC professional with a significant focus on technical writing and submission management, handling complex, data‑heavy documentation Essential experience: • Proven involvement in drug development, ideally Phase III, • Flexibility on dosage form, • Ability to work independently and deliver to tight timelines Contract details: • 6‑month contract (high likelihood of extension), • Fully remote (UK / EU), • Competitive day rate Shortlisting date: 18th March - please contact Mark Bux-Ryan for further details.

Ideally you will be a qualified accountant and have strong FP&A / Business Partnering skills combined with the ability to influence non finance colleagues. Deliver high-quality financial analysis for operations, providing the directors with timely, accurate information to support strategic deci

CMC Consulting is committed to equal opportunities.

CMC Consulting is committed to equal opportunities.

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. To characterise the companies biotherapeutic recombinant T-cell receptor based and related molecules using a wide variety of protein characterisation and mass spectrometry methods. To contribute to the development of characterisation methods for the company's biopharmaceutical products, including peptide mapping (LC-MS/MS) and intact mass spectrometry analysis. KEY RESPONSIBILITIES • Supporting drug substance and drug product impurity characterisation and identification, • Performing protein sequence and post translational modification identification, including glycosylation analysis., • Supporting drug substance and drug product process development by performing characterisation of process intermediates, • Contribute to the Development of characterisation methods of ImmTAX and other products, including peptide mapping (LC-MS/MS) and intact mass analysis, • Designing and carrying out biochemical characterisation, chemical stability and comparability studies of biologics/drug products., • Contribute to writing study protocols and reports., • Independently testing and, increasingly, leading lines of investigation. Proposing new experiments based on emerging data and other related information. Providing support on technical aspects to others., • Priorities: establishing priorities for own work and team-based projects; making decisions on prioritisation based on the overall goals of the team, department and project, using direct evidence and personal experience as guidance., • Technical Knowledge: sharing knowledge with the wider team and, across departments representing the department. May also act as a mentor to other colleagues, sharing scientific knowledge. Providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the department., • Laboratory records: ensuring that all records and information are up to date, on time and recorded to the correct standard. Supporting and encouraging others to achieve this., • Laboratory equipment: providing technical guidance to others within the team on how to use equipment most effectively., • Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners., • Adhere to safe working practices in laboratories according to Immunocore EHS policies. PERSON SPECIFICATION Experience & knowledge Essential • Experience in development of HPLC based peptide mapping methods and mass spectrometric characterisation of recombinant proteins or antibodies., • Experience of glycosylation analysis of recombinant proteins or antibodies., • Independently coordinated extensive testing of protein biomolecules., • Experienced in the characterisation of proteins expressed in both microbial and mammalian systems., • Understanding of expected post-translational modifications in biological systems., • Worked in a bench-based biopharmaceutical laboratory environment., • Experienced in assay development, • Familiar with biopharmaceutical stability study principles and interpretation thereof, • Worked and contributed actively in a diverse team environment, • Proposed and driven changes in working practices that have improved efficiency, supported teams through adoption and change, • Presented detailed scientific findings and papers to internal and external audiences Desirable • Experience of glycosylation analysis of recombinant proteins or antibodies, • Experience with late stage/commercial biopharmaceutical assay development and characterisation, • Familiar with the principles of Good Manufacturing Practise (GMP), • Presented at external conferences, • Led a small project team, formally or informally, through a change in practice including project management, • Understanding of analytical requirements to support materials for use in clinical trials Education & qualifications • Essential: BSc. Or MSc. in biochemistry, biotechnology or related discipline, • Desirable: PhD in related discipline

This is not a research role; it is a hands-on engineering role focused on making ML systems work reliably at scale. This role sits at the intersection of data engineering and ML infrastructure: youll design and operate data pipelines that feed models, and youll build the tooling that trains, deploys

Coach, mentor and help grow an existing team of Quantitative Researchers. In order to expand this team, we are looking for an experienced Quantitative Researcher to coach and mentor others whilst contributing fully towards our shared goals.

We are seeking an experienced Cloud Telephony & Contact Centre Engineer to support the migration and ongoing evolution of our contact centre capabilities within the Modern Workplace team. This role will play a key part in delivering a cloud-based contact centre migration, working under the direction

Summary of Position pMDI Product Development Scientist required to support multiple metered dose inhaler NPI projects. This is an exciting role as a pMDI Product Development Scientist required to support multiple metered dose inhaler NPI projects withinan expanding team of process and product development specialists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products and future technologies by applying their creative technical skills and scientific experience to solve complex technical challenges. Support to pMDI product development activity from early development to registration for NPI projects Provision of support for all functional data analysis and documentation activities from early development through to final submission of regulatory dossiers Job Responsibilities Plan, organise, assist/lead product development activities for Development Pharmaceutics, Stability, Specification and Data Analysis activities for pressurised metered dose inhaler NPI programmes Delivery of protocols, data interpretation and reports from early development to submission to Regulatory Authorities (including IND/IMPD/MAA/NDA submissions). Support to activities at Laboratory, GMP, Pilot and Commercial scale Minimum Requirements Bachelors degree or higher in Science based or Mathematics/Statistics based subjects from an accredited university. 2+ years of inhalation development experience. (preferably pMDI) Demonstrated ability to develop and define product development documentation for inhalation products Demonstrated data analysis and interpretation skills. Demonstrated strong oral and written communication skills. Able to multitask and remain flexible to changing project priorities. Work well both as an individual and in a team environment. Has a think outside the box mentality and is passionate about technical problem solving. Preferred Experience Familiar with CMC Documentation (IND/NDA, CTA/MAA) Familiar with metered dose inhaler products Familiar with QbD, design controls and product risk assessments TPBN1_UKTJ

The ideal candidate will have strong UK corporate tax knowledge and experience, proven skills in managing client portfolios, and the ability to lead a high-performing tax team. A leading global professional services firm is seeking an experienced Associate Tax Director to support and lead a UK corpo

Key ResponsibilitiesLead tax compliance and advisory work for a portfolio of corporate clientsManage and develop a team, including performance management, training, and recruitmentDrive operational excellence and maintain high standards of client serviceSupport business development and contribute to

Educate clients on the use of CMC’s platform, systems and trading processes to ensure maximum client satisfaction – and consequently maximum revenue for CMC. When dealing with all customers or colleagues ensure that we provide a clear, fair and consistent high quality service that presents a pro

We are looking for a dynamic and experienced Manager to join our Supply Chain & Manufacturing team, with a specialized focus on Chemistry, Manufacturing, and Controls (CMC). Supply Chain & Manufacturing Manager – Chemistry, Manufacturing, and Controls (CMC). As a Manager in our CMC team, you will

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Brief Description: Reporting into the Senior Director, Drug Substance Development, this role will provide scientific and technical leadership for drug substance development projects at various stages of the development life-cycle. Success requires application of scientific and/or engineering principles and creativity to process design and development studies, and translation into commercially feasible, reliable, and robust processes. Experience of the critical interface attributes between drug substance and drug product will be especially relevant. Activities will be performed primarily with external contract development and manufacturing organisations (CDMOs). Other responsibilities will include cross-functional team leadership and/or membership, authoring technical reports and CMC sections of regulatory dossiers, and participation in department or functional initiatives. The role will involve significant cross functional collaboration with other functions including Quality, CMC Regulatory, Manufacturing, and New Product & Technology Integration working towards agile new product introduction and ensuring all processes are understood, robust, efficient and in control. The role is both project and operations orientated. It shall require an ability to drive and deliver multiple projects concurrently. Essential Functions/Responsibilities Lead the process development and cGMP manufacture of small molecule drug substances at CDMOs Ensure adequate supply of drug substance for clinical studies and other needs. Oversee the development of robust and reliable manufacturing processes utilizing Quality by Design (QbD) principles. Oversee the synthesis of chemical entities to support clinical and non-clinical studies. Ensure that all DS processes are in line with all applicable regulations, policies, guidelines, and procedures. Represent the drug substance team on cross functional project teams as needed. Work closely with other cross-functional CMC project team members to deliver on agreed project goals. Actively contribute to functional area continuous improvement initiatives. Author and/or review drug substance sections of regulatory dossiers and technical reports. Support other Technical Operations functions to ensure a smooth transfer of technologies and products to manufacturing sites. Clearly and effectively communicate ideas and results, written and verbal, to technical and non-technical audiences. Plan, budget, execute and report on assigned projects. Develop knowledge of new pharmaceutical manufacturing processes and technologies as required in line with Jazz business objectives and share best practices within teams. Required Knowledge, Skills, and Abilities Strong record of achievement in drug substance development and manufacturing. Over ten years of experience required with a broad experience across drug development and manufacturing technologies but with specific experience related to drug substance chemical process development. Demonstrated technical expertise in chemical process development and new product introduction. Demonstrated technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design to support process development objectives. Demonstrated troubleshooting and problem-solving skills. Experience of CMC regulatory requirements for pharmaceutical products. Demonstrated track record of training and coaching colleagues to improve overall team process knowledge. Demonstrated track record of delivering positive results on a consistent basis. Proven project management skills for technical programs. Experience in managing and maintaining budgets desirable. Experience in defending processes, procedures, and investigation during FDA/EMA (and other competent authorities) inspections desirable. Capability of grasping complex technical issues and make sound decisions based on data and information from various sources. Knowledge of formulation development and/or large molecule technologies would be advantageous. Excellent written and verbal communication skills. Required/Preferred Education and Licenses Bachelor’s degree and Masters or PhD in Chemistry. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here

Strong understanding of CMC regulatory frameworks, quality systems, and manufacturing processes. If you are a detail‑driven Regulatory CMC specialist who thrives in a flexible freelance environment, we would love to hear from you. Regulatory CMC Technical Writer.

CMC Consulting is partnering with a leading UK manufacturing business experiencing exciting growth and seeking an analytically minded FP&A Analyst. CMC Consulting is committed to equal opportunities.

Extensive experience in CMC strategy and a minimum of ten years of experience in CMC development and regulatory compliance. Scendea is seeking a highly motivated individual to join our global team as a full-time Principal Consultant (CMC). Provide strategic, technical and regulatory advice/services

To act as the CMC Regulatory Lead on CMC Teams, representing the CMC Regulatory viewpoint and expertise on the CMC Team;. As a key member of the Regulatory Affairs CMC team, the candidate will have responsibility for developing CMC regulatory strategy for the clinical portfolio from a Regulatory CMC

Principal / Senior Regulatory Affairs CMC Consultant. As a Principal or Senior Regulatory Affairs CMC Consultant, you will play a key leadership role, providing high-level regulatory and technical guidance for complex therapeutics. Provide strategic, technical, and regulatory CMC advice to clients,

Suitable candidates must have the right to work in the UK and a strong background in CMC and MSAT.

Group Accountant – First Move from Practice.This role offers an excellent first move into industry for an ACA‑qualified (or recently qualified) accountant seeking exposure to commercial finance within a multi‑entity organisation.The position provides hands‑on involvement in core financial ac

A leading financial services firm in Greater London is seeking an experienced Senior Project Manager to lead large-scale change initiatives.This high-impact role requires overseeing complex, cross-functional programmes and managing the entire project lifecycle.The ideal candidate will possess strong

A fast-growing SME in Finance based in Dacorum is looking for a proactive finance professional to join their expanding team.Key responsibilities include preparing and maintaining accounts, reconciling journals, and managing balance sheets.The ideal candidate should have 2-3 years of relevant finance

Minimum 10 years of experience in CMC within the pharmaceutical industry and CMC regulatory technical writing. Senior CMC Regulatory Technical Writer. You will play a key role in translating complex CMC scientific and technical data into clear, concise, and compliant regulatory documentation (Module

A leading financial technology company seeks a Security Platform Engineering Manager to enhance its Platform Engineering capabilities.This role involves defining and operating reusable security capabilities for customer-facing services.The ideal candidate will have deep expertise in securing cloud n

A leading global professional services firm is seeking an experienced Associate Tax Director to manage a UK corporate tax team.Responsibilities include leading tax compliance for corporate clients, managing team performance, and driving operational excellence.Ideal candidates will be ICAEW, ACCA, or

Since launching in 1989, CMC Markets (CMC) has become one of the world's leading online financial trading businesses. CMC is listed on the London Stock Exchanges and serves retail and institutional clients through regulated offices and branches in 13 countries. CMC offers an award winning online and

A leading global professional services firm is seeking an experienced Associate Tax Director to support and lead a UK corporate tax team.The role involves managing a portfolio of complex clients, overseeing compliance and advisory matters, and contributing to the strategic direction of the departmen

Homerton Neonatal Unit, in partnership with Roald Dahl's Marvellous Children's Charity, is establishing a pioneering Band 8a Neonatal Nurse Specialist role to lead care for neonates with complex medical needs (CMC) across North East London. Lead and influence care pathways, guidelines, and standards

CMC Markets requires a suitably skilled Liquidity Risk Manager responsible for the assisting with the implementation of an effective Liquidity Risk framework. When dealing with all customers, clients or colleagues ensure that we provide a clear, fair and consistent high-quality service that presents

A leading healthcare provider is seeking a skilled Roald Dahl Neonatal CMC Nurse Specialist to provide expert clinical leadership for neonates across North East London.

ML Ops / Data Engineer page is loaded## ML Ops / Data Engineerlocations: Londontime type: Full timeposted on: Posted Yesterdayjob requisition id: CMC5104# ML Ops / Data EngineerRole OverviewWe’re hiring an ML Ops Engineer / Data Engineer to own the reliability, scalability, and

A global, media and entertainment business is seeking a Commercial Finance Analyst to support a key revenue-generating function within a fast-paced, international environment.This role offers strong exposure to senior stakeholders and the opportunity to work closely with commercial teams to drive pe