Carbon 60

Systems Engineer Bristol (Filton) Upto 75 per hour Inside IR35 6-Month Contract Strong Extension Potential We're seeking an experienced Systems Engineer to join a cutting-edge defence programme developing next-generation Laser Directed Energy Weapon (LDEW) capability. This is a high-profile project offering the opportunity to work at the forefront of advanced defence technology, supporting the development of complex systems and working closely with systems engineering, software and algorithm development teams. The Role As a Systems Engineer, you will play a key role in the development of a critical Command & Control subsystem, supporting requirements capture, functional architecture development and systems engineering activities across the project lifecycle. Key Responsibilities Capture, derive and refine system and subsystem requirements. Support the development of functional architectures and system designs. Work collaboratively within multi-disciplinary engineering teams. Identify and manage risks, opportunities, assumptions and issues. Contribute to technical reviews, project reporting and engineering governance activities. Engage with stakeholders across systems engineering, software and algorithm disciplines. Support the delivery of complex engineering solutions within demanding timescales. Required Experience Systems engineering or product development experience. Strong stakeholder management and communication skills. Experience across the systems engineering lifecycle. Functional design and development experience. Experience working within cross-functional engineering teams. Practical knowledge of IBM DOORS, IBM Rhapsody and/or IBM Engineering Workflow Management. Candidates must be eligible for UK Security Clearance This is an excellent opportunity to join a pioneering defence programme and contribute to the development of advanced technology within a highly collaborative engineering environment. Apply now for immediate consideration. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Senior HSE Advisor Senior HSE Advisor Location: Portsmouth Area Salary: 45,000 - 55,000 DOE Contract: Permanent Hours: Monday to Friday, 7:30am to 4:15pm (9-Day Fortnight) Are you an experienced HSE professional who enjoys balancing compliance, administration and hands-on engagement with operational teams? Our client, a leading aerospace manufacturer producing critical safety equipment and helicopter fuel systems, is looking to appoint a Senior HSE Advisor to support the continued development of a positive and proactive safety culture across its production operation. This role is ideal for someone who is equally comfortable maintaining compliance systems and documentation as they are building strong relationships on the shop floor and influencing safe behaviours across the workforce. The Role Reporting into the Facilities & Maintenance Manager, you will play a key role in developing, implementing and continuously improving the site's Health, Safety and Environmental Management Systems. Responsibilities include: Supporting compliance with HSE legislation and regulatory requirements. Managing risk assessments, COSHH and safe systems of work. Monitoring HSE performance and supporting continuous improvement initiatives. Conducting audits, inspections and behavioural observations. Supporting incident investigations and corrective actions. Coordinating HSE training and maintaining compliance records. Building strong relationships with production teams and operational leaders. Driving workforce engagement and promoting positive safety behaviours across the site. About You NEBOSH General Certificate as a minimum. Previous experience within manufacturing, engineering, aerospace or another safety-critical environment. Strong knowledge of UK Health & Safety legislation. Excellent communication and influencing skills. Comfortable working both in an administrative/compliance capacity and actively on the shop floor. Proactive, pragmatic and solutions-focused approach. Benefits Salary of 45,000 - 55,000 depending on experience. 25 days annual leave plus bank holidays. 9-day working fortnight. Company pension scheme. Employee Assistance Programme. Additional health and wellbeing benefits. Opportunity to join a market-leading aerospace manufacturing business supplying critical products to customers worldwide. If you are looking for a role where you can genuinely influence safety culture while working within a highly respected aerospace manufacturing environment, we would love to hear from you. Apply today for immediate consideration. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Senior HSE Advisor (Interim Contract) Senior HSE Advisor Contract: Initial 3-Month Contract (Potential Extension) Location: Portsmouth Area Hours: Monday to Friday, 7:30am to 4:15pm (9-Day Fortnight) Rate: Competitive Hourly or Daily Rate (DOE) Our client, a leading aerospace manufacturing company specialising in mission-critical helicopter fuel systems and safety equipment, is seeking an experienced Senior HSE Advisor to join their team on an interim basis. This is an excellent opportunity for an experienced HSE professional to make an immediate impact within a highly regulated manufacturing environment. Due to the imminent departure of the current postholder, we are looking to appoint someone as soon as possible. Key Responsibilities Ensure compliance with UK Health, Safety and Environmental legislation and company standards. Lead and support audits, inspections and workplace monitoring activities. Manage risk assessments, COSHH assessments and safe systems of work. Support incident investigations, root cause analysis and corrective actions. Maintain HSE records, reporting systems and compliance documentation. Conduct shop floor inspections, behavioural observations and workforce engagement activities. Deliver practical HSE guidance and support to operational teams. Promote a proactive safety culture throughout the site. About You NEBOSH General Certificate (minimum requirement). Previous experience within manufacturing, engineering, aerospace or similar industrial environments. Strong knowledge of UK HSE legislation. Experience conducting risk assessments and incident investigations. Comfortable working both strategically and hands-on within a production environment. Strong communication and stakeholder management skills. What's on Offer? Immediate start available. Initial 3-month contract with potential extension. Flexible engagement through an hourly or daily rate. 9-day fortnight working pattern. Opportunity to support a leading aerospace manufacturing operation. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Embedded Software Engineer We're seeking a talented engineer to join a world-leading navigation and maritime technology organisation, helping to develop the next generation of radar systems used across commercial and defence maritime environments worldwide. This is an exciting opportunity to work at the forefront of embedded software development, contributing to innovative radar and navigation solutions that enhance safety, operational effectiveness, and mission success at sea. What You'll Be Doing Developing embedded software for next-generation radar and navigation products Working closely with software and hardware engineering teams to deliver innovative solutions Supporting system integration and product testing activities Participating in Agile development processes, sprint planning, and code reviews Contributing to the evolution of advanced maritime technologies used globally What We're Looking For Solid experience in embedded software engineering Strong C++ and C# development skills Experience working with real-time, multi-threaded systems Knowledge of Linux environments, Bash scripting, and Python Understanding of networking protocols including TCP/IP and UDP Experience with OpenEmbedded, Bitbake, Makefiles, and embedded Linux development Ability to work collaboratively within a multi-disciplinary engineering team Desirable Experience Radar systems development ASTERIX CAT240 protocol RF transceiver integration U-Boot and embedded bootloader technologies Wireshark and network analysis tools Wt web GUI libraries Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

A new opportunity exists to join the business management team for Industrial Supply Chain in Broughton, UK. PIOX is the business management function for the Airbus Supply, logistics and transport teams for all Airbus commercial sites and in charge of Resource management Budget planning & controlling Performance and Risk Management Digital tools and dashboard AOS - Airbus Operating System Resilience & Business Continuity for logistics & transportation Sustainability roadmap (CO2, waste, ) The position will be a great opportunity to gain personal visibility and grow a wider understanding of logistics and supply management in an international environment. Your tasks: Overseeing budgeting and forecasting Supporting operational financial planning Reporting financial risks and ops Creating, maintaining and improving dashboards Supporting business case creation Skills required: Experience leading or supporting annual budgeting, forecasting, and long-range financial planning processes. Strong background in financial performance analysis and identifying financial risks and opportunities. Demonstrated experience creating business cases, investment appraisals, and financial models to support decision-making. Experience developing and maintaining management dashboards and performance reporting tools. Ability to translate complex financial data into meaningful commercial insights and recommendations. Experience working in a fast-paced operational or project-based environment. Stakeholder Management Experience working with operational leaders and non-finance stakeholders. Strong communication skills with the ability to present financial information clearly to senior management. Ability to influence decision-making through insight-led recommendations. Strong collaboration and relationship-building skills across multiple business functions. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Analytical Quality & Compliance Coordinator Location: Sandwich, Kent Employment Type: Permanent Working Pattern: Full-time, On-site (5 days per week) The Opportunity Synergy is seeking an Analytical Quality & Compliance Coordinator to support a major analytical services programme delivered by our scientific team in Sandwich, Kent. This is an excellent opportunity for a quality-focused scientist or compliance professional looking to develop their career within a GMP-regulated pharmaceutical laboratory environment. You will play a key role in maintaining quality systems, ensuring compliance with regulatory requirements, supporting inspections and audits, and driving continuous improvement across the analytical function. Key Responsibilities Coordinate analytical quality and compliance activities across the department. Lead and facilitate regular compliance meetings, tracking quality metrics and actions. Author, review and maintain SOPs, training modules and GMP documentation. Support the review and implementation of compendial updates. Coordinate internal and external audits, inspections and associated actions. Manage laboratory notebooks, equipment logbooks and controlled documentation processes. Maintain training curricula and ensure appropriate training assignments across analytical teams. Support GMP compliance activities and continuous improvement initiatives. Collaborate with multidisciplinary scientific and quality teams to ensure inspection readiness and ongoing compliance. Manage the issuance and control of regulated documentation provided to external partners and stakeholders. About You To be successful in this role, you will have: A degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensic Science, or a related scientific discipline, or equivalent industry experience. Experience working within a GMP-regulated pharmaceutical, biotechnology or laboratory environment. A strong understanding of cGMP requirements and quality systems. Experience authoring SOPs, controlled documents or training materials. Knowledge of analytical laboratory techniques, including HPLC. Excellent organisational skills and attention to detail. Strong written and verbal communication skills. The ability to manage multiple priorities and work effectively both independently and as part of a team. Good Microsoft Office skills, particularly Excel, Word and PowerPoint. A proactive approach with a focus on quality, compliance and continuous improvement. Why Join Synergy? Permanent opportunity with a growing scientific services organisation. Work within a high-performing analytical science environment supporting pharmaceutical operations. Develop expertise across quality systems, compliance, audits, inspections and regulatory processes. Join a collaborative and supportive team with excellent opportunities for professional growth and development. Play a key role in delivering critical scientific services within a regulated industry. Apply Now If you have a scientific background, GMP experience and a passion for quality and compliance, we'd love to hear from you. Apply today to join Synergy's analytical services team in Sandwich and take the next step in your quality and compliance career. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: QC Specialist Microbiology Location: Speke, Liverpool. Hours: M-F, 37.5 hrs p/w Rate: 15.04 p/h Contract: until end of Dec 2026 SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Microbiologist to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate ideally with some GMP experience to further their career. Main responsibilities: Performing a range of Quality Control tests in line with to GMP regulations. Performing routine QC testing: Environmental Monitoring Plates, Utilities Sampling and Testing, Sterility testing Bioburden testing, Selective organism testing Endotoxin testing Documenting laboratory results in an accurate and timely manner. Complying with GMP regulatory requirements at all times. Key requirements: Educated to BSc /MSc level in a relevant scientific subject Industry experience (12 months + desired) Experience of working to GMP/pharmaceutical regulatory requirements is highly desirable Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Scientist II - Laboratory Services Location: Deeside, UK Contract Type: Contract (5 Months) Start Date: ASAP Pay Rate: 142.32 per day (PAYE) About the Role We are seeking a Scientist II - Laboratory Services to join our Technology & Innovation team at our Global Development Centre in Deeside. This is an excellent opportunity for a scientifically minded professional to contribute to the stability testing of medical devices and skincare products, supporting product shelf-life claims, regulatory compliance, and product labelling requirements. The successful candidate will perform physical and analytical stability testing in accordance with established study protocols, SOPs, quality standards, and regulatory requirements. Working within a GMP/GLP laboratory environment, you will play a key role in generating, analysing, and reporting stability data while contributing to continuous improvement initiatives across the laboratory. Key Responsibilities Stability Testing & Analysis Perform physical and analytical stability testing on existing and new medical devices and skincare products. Analyse, interpret, document, and report laboratory data to GMP/GLP standards. Collate stability data and support the generation of technical and stability reports. Assist in the preparation of shelf-life plans, stability protocols, and associated reports. Suggest appropriate real-time and accelerated ageing programmes for study concepts. Coordinate and organise stability studies from initiation through to completion. Support planned and ad hoc stability sample set-downs and pull requests. Laboratory Operations Maintain, calibrate, and support laboratory equipment while ensuring quality records remain up to date. Work confidently with a broad range of analytical instrumentation, including balances, pipettes, HPLC, and ICP-MS. Support storage and retrieval activities for stability samples. Assist with maintenance, servicing, and calibration activities completed by external suppliers. Monitor laboratory inventory levels and request replenishment of consumables, chemicals, and reagents as required. Quality & Compliance Maintain compliance with ISO 13485, ISO 9001, GMP, and GLP requirements. Draft and maintain stability documentation, including protocols and reports. Prepare quality documentation such as Change Controls, Non-Conformances, and Out of Specification (OOS) reports. Participate in laboratory investigations and support root cause analysis and troubleshooting activities. Provide timely support during internal and external audits. Ensure laboratory activities comply with site Health & Safety, environmental, and quality procedures. Continuous Improvement & Team Support Support ongoing improvements to stability testing processes and operating procedures. Actively participate in Lean and 6S initiatives within the laboratory environment. Train and support new or less experienced team members on test methods, equipment use, and calibration procedures. Promote a safe working environment and raise near misses where appropriate. Provide technical input into stability studies under the guidance of senior scientists. About You To be successful in this role, you will be a detail-oriented scientist with experience working within a regulated laboratory environment. You will possess strong analytical skills, a commitment to quality, and the ability to effectively manage multiple priorities in a fast-paced setting. Essential Skills & Experience BSc degree (or equivalent) in a scientific discipline such as Chemistry, Biology, or a related field. 1-2 years of experience within the Medical Device, Pharmaceutical, or related Life Sciences industry, ideally in an R&D or product development environment. Experience following laboratory procedures, protocols, SOPs, and technical documentation. Knowledge of GMP, GLP, and quality management systems. Understanding of FDA, ICH, and European regulatory requirements. Experience using laboratory analytical equipment and instrumentation. Strong written and verbal communication skills. Proficiency in Microsoft Office, particularly Word and Excel. Experience using computerised systems for data management and record keeping. Excellent organisational skills with the ability to prioritise changing workloads. Positive, proactive attitude with a continuous improvement mindset. Desirable Experience Experience working with HPLC and ICP-MS instrumentation. Exposure to stability testing programmes within medical device or pharmaceutical development. Experience participating in audits and laboratory investigations. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Groundworker / Civil Operative Location: Bedfordshire Start Date: Immediate Start Available Duration: Ongoing Contract Opportunity Rate: Competitive Outside IR35 Immediate Opportunities for Experienced Groundworkers We are seeking experienced Multi-Skilled Civils Operatives to support infrastructure repair and maintenance works on a major industrial site in Bedfordshire. This is not a labouring role. We are looking for individuals with proven experience in groundworks, civils repairs, drainage works and reinstatement activities who can work safely, efficiently and with minimal supervision. The successful candidates will join an established team carrying out a variety of civils maintenance works, including repairs to existing assets, chamber and manhole works, sealing activities and general site improvements. Key Responsibilities Carrying out general civils repair and maintenance works Manhole, chamber and drainage repairs Sealing and reinstatement works Minor concrete repairs and finishing activities Groundworks associated with site maintenance projects General infrastructure repairs and making-good works Supporting safe delivery of works within a live operational environment Maintaining high standards of housekeeping and site safety Essential Experience & Qualifications Valid CSCS Card 2+ years' experience in groundworks, civil engineering or infrastructure maintenance Practical experience of drainage, chamber and manhole repair works Experience undertaking reinstatement and repair activities Ability to work from site instructions and complete work with minimal supervision Good understanding of construction health and safety requirements Reliable, flexible and able to work effectively within a small site team Full UK Working Rights Desirable Experience working on industrial, energy, utilities or infrastructure sites First Aid qualification CPCS or NPORS plant tickets Street Works (NRSWA) accreditation What We Offer Immediate start opportunities Competitive rates Ongoing project work Established and supportive site team Opportunity to work on a significant infrastructure maintenance programme We are looking to mobilise operatives urgently, with candidates available to start immediately particularly encouraged to apply. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Manager - Regulatory Affairs Submission Management Contract: Temporary - 12 months (extension possible) Location: Maidenhead - hybrid working (or remote if needed) Rate: (INSIDE IR35) - circa. 22-25 per hour (PAYE) SRG are seeking a Regulatory Affairs professional with Submission Management skills & experience to assist a leading pharmaceutical company on a temporary basis. Join a dynamic regulatory affairs team and play a pivotal role in delivering complex regulatory submissions that support the development, approval, and life-cycle management of innovative healthcare products. Key Responsibilities Lead and manage complex regulatory submission projects, ensuring high-quality dossiers are delivered on time and in line with regulatory requirements. Act as the primary regulatory submission management contact for cross-functional project teams, providing guidance on processes, timelines, and deliverables. Coordinate and facilitate submission planning meetings, driving progress across multiple concurrent projects and stakeholders. Oversee publishing activities and collaborate with external publishing partners to ensure successful submission delivery. Perform quality reviews of published submissions, ensuring compliance with technical standards and regulatory authority requirements. Contribute to continuous improvement initiatives, enhancing regulatory processes, standards, and systems. Skills & Experience Required Bachelor's degree or equivalent combination of education and relevant industry experience. Experience within the pharmaceutical, biotechnology, healthcare, or related regulated industry. Strong project management skills, with experience managing complex, cross-functional activities and competing priorities. Knowledge of regulatory operations, submission management, and/or submission publishing processes. Excellent written and verbal communication skills, with the ability to influence stakeholders in a matrix environment. Demonstrated leadership capability, including mentoring colleagues and driving process improvements. PMP and/or RAC certification is advantageous. To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed) Umbrella also possible - please enquire for more information Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Dispensary - Technician 2 Location: Jealotts Hill, Bracknell Rate: 13.62 per hour Contract Length: 12 months Start Date: ASAP Duties The preparation of samples for Syngenta's 'Screening Deck' project. The key tasks are dry sample dispensing at a weigh station ahead of solubilisation and reformat to 2D Matrix tubes. The preparation of sample solutions in mM concentrations ready for shipping to a CRO. Day to day the role will entail the picking, dispensing, reformatting and shipping of samples. Skills Experience of working in a laboratory environment in a similar industry, or at college. Moderate level IT skills: Use of MS Excel, querying and reporting applications, laboratory LIMS systems (Eg, Mosaic) Some experience of using Tecan liquid handling systems is highly desirable. Education A Levels BSc Degree level if first job since graduation. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Scientist II - Physical Testing Location: Deeside, UK Contract Type: Contract (12 Months) Start Date: ASAP Pay Rate: 142.32 per day (PAYE) About the Role We are seeking a Scientist II to join our Technology & Innovation team at our Global Development Centre in Deeside. This is an excellent opportunity for a scientifically minded professional to contribute to the stability testing of medical devices and skincare products, supporting product shelf-life claims, regulatory compliance, and product labelling requirements. The successful candidate will perform physical and analytical stability testing in accordance with established study protocols, SOPs, quality standards, and regulatory requirements. Working within a GMP/GLP laboratory environment, you will play a key role in generating, analysing, and reporting stability data while contributing to continuous improvement initiatives across the laboratory. Key Responsibilities Stability Testing & Analysis Perform physical and analytical stability testing on existing and new medical devices and skincare products. Analyse, interpret, document, and report laboratory data to GMP/GLP standards. Collate stability data and support the generation of technical and stability reports. Assist in the preparation of shelf-life plans, stability protocols, and associated reports. Suggest appropriate real-time and accelerated ageing programmes for study concepts. Coordinate and organise stability studies from initiation through to completion. Support planned and ad hoc stability sample set-downs and pull requests. Laboratory Operations Maintain, calibrate, and support laboratory equipment while ensuring quality records remain up to date. Work confidently with a broad range of analytical instrumentation, including balances, pipettes, HPLC, and ICP-MS. Support storage and retrieval activities for stability samples. Assist with maintenance, servicing, and calibration activities completed by external suppliers. Monitor laboratory inventory levels and request replenishment of consumables, chemicals, and reagents as required. Quality & Compliance Maintain compliance with ISO 13485, ISO 9001, GMP, and GLP requirements. Draft and maintain stability documentation, including protocols and reports. Prepare quality documentation such as Change Controls, Non-Conformances, and Out of Specification (OOS) reports. Participate in laboratory investigations and support root cause analysis and troubleshooting activities. Provide timely support during internal and external audits. Ensure laboratory activities comply with site Health & Safety, environmental, and quality procedures. Continuous Improvement & Team Support Support ongoing improvements to stability testing processes and operating procedures. Actively participate in Lean and 6S initiatives within the laboratory environment. Train and support new or less experienced team members on test methods, equipment use, and calibration procedures. Promote a safe working environment and raise near misses where appropriate. Provide technical input into stability studies under the guidance of senior scientists. About You To be successful in this role, you will be a detail-oriented scientist with experience working within a regulated laboratory environment. You will possess strong analytical skills, a commitment to quality, and the ability to effectively manage multiple priorities in a fast-paced setting. Essential Skills & Experience BSc degree (or equivalent) in a scientific discipline such as Chemistry, Biology, or a related field. 1-2 years of experience within the Medical Device, Pharmaceutical, or related Life Sciences industry, ideally in an R&D or product development environment. Experience following laboratory procedures, protocols, SOPs, and technical documentation. Knowledge of GMP, GLP, and quality management systems. Understanding of FDA, ICH, and European regulatory requirements. Experience using laboratory analytical equipment and instrumentation. Strong written and verbal communication skills. Proficiency in Microsoft Office, particularly Word and Excel. Experience using computerised systems for data management and record keeping. Excellent organisational skills with the ability to prioritise changing workloads. Positive, proactive attitude with a continuous improvement mindset. Desirable Experience Experience working with HPLC and ICP-MS instrumentation. Exposure to stability testing programmes within medical device or pharmaceutical development. Experience participating in audits and laboratory investigations. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Manager - HTA, Value & Evidence (Migraine) Type: Temporary Duration: Up to 23 months Location: Tadworth, Surrey Rate: up to 37.86 per hour (Umbrella, INSIDE IR35 - PAYE option also available) Join a leading global pharmaceutical organisation dedicated to delivering innovative therapies that improve patients' lives on a long-term contract. This role sits within the Health Technology Assessment (HTA), Value & Evidence team, supporting global migraine programmes through a blend of scientific research, evidence generation, and operational excellence. Key Responsibilities Manage real-world evidence (RWE) studies aligned to global evidence generation strategies, ensuring delivery to time and quality standards Support the design, analysis, and interpretation of health economics and outcomes research in collaboration with internal experts and external stakeholders Oversee publication planning and delivery, including manuscript development and journal submission processes Coordinate project operations including budgets, contracts, invoicing, and tracking systems to ensure effective programme delivery Act as a key point of contact for vendors, key opinion leaders and internal stakeholders, managing timelines and communications Maintain study documentation, ensure quality control, and support compliance across global systems and registries Skills & Experience Required Advanced degree (MSc or PhD) in health economics, epidemiology, public health, or a related discipline Experience in HEOR, RWE, or health services research within pharma, consulting, or academia (typically 2+ years) Strong understanding of study design, data analysis, and evidence generation methodologies Proven project management skills with the ability to manage multiple priorities and stakeholders effectively Excellent written and verbal communication skills, with experience supporting publications desirable Highly organised, detail-oriented, and able to work independently in a fast-paced environment To Apply Please click below and/or to discuss further, contact Theo Charles on (phone number removed) Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Job Title: Medical Affairs Graduate Job Type: 12 Months Fixed Term Contract Employment Start Date: ASAP Hours of work: Mon - Fri (37.5 hours a week) Onsite requirement: This will be a hybrid role, with at least 3 days per week on site Location: London, UK Salary: 31,050 per annum; holidays, sick pay, pension An excellent opportunity for a talented graduate to start a career in medical affairs with a global healthcare leader, our client has one of the most exciting product pipelines in the industry today. Our mission is to improve patients' lives by providing customers with innovative science and differentiated healthcare solutions delivered by diverse and engaged talent with integrity, passion and focus on performance. Creativity and diversity are encouraged, impact is recognised, success is celebrated, and people feel valued and listened to. Job Purpose As a Medical Affairs Graduate , you will play a crucial role in supporting our medical team for the Cardiovascular Therapeutic Area (TA). Your responsibilities will include, but are not limited to: Building a strong knowledge base of the TA related disease area, typical Medical Affairs activities, the healthcare system, and ABPI code. Supporting the implementation of the Medical Affairs Plan, which includes activities like advisory boards, medical education meetings and projects, data generation projects, and ensuring congress excellence by working with the broader team (field & Head Office). Collaborating with the Medical Affairs team to review non-promotional materials, ensuring the scientific integrity of their content. Collaborate with cross-functional colleagues including Commercial, Market Access, Regulatory Affairs, Pharmacovigilance and Clinical Development teams to support delivery of integrated medical plans. Supporting the delivery of medical plans by tagging, uploading and referencing medical educational materials in the internal approval system. Developing high-quality and timely briefing materials/training on relevant appropriate data, and delivering internal training when required. Providing administrative support as needed, such as budget management for projects and logistics, raising purchase orders, arranging contracts with 3rd party vendors, healthcare organisation and clinicians, coordinating team meetings, organising itineraries and logistics for ongoing activities. Enabling our field medical team to deliver on impactful scientific data releases and coherent scientific narratives through content development and approvals, for example. Skills & Experience: To be considered for the Medical Affairs Graduate , you'll need the following skills and experience: Recently graduated from a UK university within the last 2 years, with a degree in Life Sciences, Medicine, or Pharmacy (completed pre-registration pharmacy exams). Clear motivation and ambition to gain experience in a medical affairs environment. Experience within the UK healthcare and/or pharmaceuticals environment is advantageous, although not necessary. Ability to demonstrate transferable skills to the business environment, such as good time management and teamwork, through previous work experience, academic achievements, or extracurricular activities. Strong prioritisation skills, with the ability to effectively manage multiple priorities and demonstrate attention to detail, even under tight deadlines. Collaborative mindset, with the ability to develop effective relationships with team members and customers, gaining trust and credibility quickly. You should be comfortable working with people of all levels and backgrounds as a valuable member of a cross-functional team. Customer-focused approach, delivering high-quality projects and activities to both internal and external stakeholders. You should be aware of and responsive to their needs. IT proficiency and highly proficient in Microsoft Office suite (Outlook, Excel, PowerPoint, and Word). Fluency in English - Verbal and Written The successful candidate will benefit from: Team oriented atmosphere Cutting edge science Working with diverse people and teams Development opportunities Making a difference to patient's lives Additional Information Please ensure that you are willing and able to live within commutable distance of the company site before applying. This placement is based in their London, UK offices, and you will be required to be in the office a minimum of 12 days per month, to aid your development in working with and learning from your team. You will need to be eligible to work in the United Kingdom. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Principal Supply Chain Subcontract Specialist Location: Cheltenham Salary: up to 55,000 About the Role Our client are recruiting for a Principal Supply Chain Subcontract Specialist to join a leading organisation operating within a highly regulated and technology-driven environment. This role sits at the heart of bid and capture activity, partnering with Business Development, Programme, Finance and Bid teams to develop competitive, deliverable supply chain strategies that support future business growth. You will play a key role in identifying, engaging and managing suppliers, ensuring supply chain capability aligns with both current programme delivery and future opportunities. This is an excellent opportunity for a commercially minded procurement or supply chain professional who enjoys influencing strategy, negotiating value and working within complex stakeholder environments. Key Responsibilities Develop and maintain a network of suppliers aligned to current and future business requirements. Support Business Development teams in shaping supply chain strategies for bids and new opportunities. Identify, assess and engage suppliers, ensuring the right capability, innovation and value proposition is incorporated into bids. Act as the primary point of contact for supplier engagement throughout the bid lifecycle. Assist with the development and implementation of contracts in line with procurement policies and governance requirements. Support bid planning, reporting and governance activities to ensure delivery against deadlines. Promote responsible sourcing and social value initiatives across the supply chain. Requirements Essential Previous experience supporting bids, proposals or business-winning activities within a regulated environment. Strong supplier relationship management and stakeholder engagement skills. Proven negotiation experience with the ability to deliver commercial value. Good understanding of procurement principles and contract management. Highly organised with the ability to manage multiple priorities in a fast-paced environment. Strong communication and influencing skills. Desirable Experience within defence, engineering, aerospace or other highly regulated sectors. CIPS Level 5 qualification (or working towards). Commercial management accreditation (e.g. WorldCC). Knowledge of international trade compliance regulations. Security Requirements Due to the nature of the work, applicants must be eligible to obtain and maintain UK Government Security Clearance (SC). Benefits Flexible and hybrid working options Compressed working arrangements available Private healthcare Health cash plan Holiday buy and sell scheme Annual bonus opportunity Ongoing training and career development Clear progression opportunities within a growing organisation Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Electrical Compliance Engineer Salary: Competitive About the Opportunity We're working with a well-established engineering and compliance specialist that is looking to expand its field-based team with the addition of an experienced Electrical Compliance Engineer. This is an excellent opportunity for someone who enjoys a varied workload, autonomy in their day-to-day activities, and the chance to work across a diverse range of commercial and industrial environments. You'll be responsible for delivering electrical compliance services, technical inspections, and detailed reporting while maintaining the highest standards of safety and professionalism. Unlike many service roles, most assignments are completed at a single site each day, allowing you to focus on delivering quality work rather than spending your time travelling between multiple locations. The Role As a Electrical Compliance Engineer, you will: Conduct electrical compliance inspections and condition assessments across commercial and industrial facilities Produce detailed technical reports and supporting documentation Carry out associated surveying and fault-identification activities where required Ensure all job records, reports, and paperwork are completed accurately and submitted within agreed timescales Build and maintain strong relationships with site contacts and key stakeholders Support the development of junior engineers through coaching and mentoring Uphold high standards of health, safety, and technical compliance Effectively manage company equipment, vehicles, and administrative responsibilities What We're Looking For We're keen to speak with electrically qualified professionals who can demonstrate experience in inspection, testing, verification, or electrical compliance activities within commercial or industrial environments. You'll also have: Relevant electrical qualifications and inspection/testing credentials Strong knowledge of current electrical regulations and industry standards The ability to accurately assess electrical installations and identify non-compliance issues Excellent attention to detail and report-writing skills A proactive and organised approach to your workload The ability to work independently and manage your own site schedule A full UK driving licence Flexibility to travel and occasionally undertake work outside standard hours when required What's in It for You? Competitive salary Overtime paid at 1.5X standard rate Company vehicle and fuel card Contributory pension scheme Investment in professional development and ongoing technical training Clear opportunities for career progression Stable, long-term opportunity with an established and growing business Diverse project portfolio across commercial and industrial sectors Apply Now If you're looking for a role that offers variety, independence, and the opportunity to further develop your technical expertise within a supportive environment, we'd love to hear from you. Applications are welcomed from experienced electrical professionals, and we encourage you to apply even if your experience doesn't align perfectly with every requirement listed above. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

IT Infrastructure Engineer (Contract) Location: Portsmouth (Onsite) Travel: Occasional travel to dockyards and customer sites across the UK (advance notice provided) Security Clearance: Active SC Clearance required to start (candidates already holding SC clearance highly desirable) Contract Type: Contract Overview We are looking for an experienced Infrastructure Engineer to support the delivery, deployment and ongoing support of a modern hosting and infrastructure platform within a secure defence environment. Working as part of a collaborative technical team, you will play a key role in building, deploying and supporting enterprise infrastructure services while ensuring a high standard of service delivery. This role is primarily based onsite in Portsmouth, with occasional travel required for installation and deployment activities across the UK. Key Responsibilities Build, deploy and support enterprise infrastructure platforms. Administer VMware hosted services and virtual environments. Provide 1st, 2nd and 3rd line support for infrastructure services. Support and maintain Microsoft Windows Server and Active Directory environments. Configure and manage Dell server hardware and iDRAC. Maintain technical and operational documentation. Support asset management, logistics and supplier engagement activities. Participate in ITIL-based change management processes. Work closely with project and operational teams to deliver infrastructure services. Support onsite installation and deployment activities when required. Essential Skills & Experience Strong experience administering VMware Cloud Foundation (VCF) environments. Good working knowledge of VMware vCenter 7.0 or later. Experience supporting Microsoft Windows Server 2019/2022. Strong Active Directory administration experience. Knowledge of Dell server hardware and iDRAC management. Experience providing 2nd and 3rd line support within enterprise environments. Ability to maintain accurate technical documentation. Experience working within ITIL change management processes. Strong communication skills and the ability to work effectively within a team. Desirable Skills Experience using Remedy. Office automation and documentation management skills. Experience supporting IT services within defence, maritime or secure environments. Ability to work independently and manage competing priorities. Strong stakeholder management and supplier engagement skills. Qualifications ITIL Foundation certification. Microsoft certification (MCSA or equivalent preferred). VMware Cloud Foundation (VCF) certification desirable. Security Requirements Due to the nature of the programme, candidates must hold active SC Clearance or be eligible for immediate transfer. Candidates already holding valid SC Clearance are strongly preferred. Apply If you have proven experience supporting VMware, Windows Server and enterprise infrastructure environments and are looking for an opportunity to contribute to a high-profile defence programme, we would be keen to hear from you. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Medical Director, Oncology Clinical Development Contract: Temporary - 6 months Location: Remote - UK (client based in London) Rate: (INSIDE IR35) - circa. 1125 per day (Umbrella) SRG are seeking an experienced Clinical Development Medical Director with Oncology expertise to support a leading pharmaceutical company on a temporary basis. Join a team dedicated to advancing innovative oncology therapies through high quality clinical research. This is an exciting opportunity for a physician leader to shape clinical development strategy, drive global oncology trials, and collaborate with leading scientific experts. Key Responsibilities Lead the design, development, and execution of Phase I-III oncology clinical trials. Provide medical oversight and monitoring for ongoing studies, including safety and eligibility reviews. Contribute to clinical development strategies that support regulatory submissions and successful product launches. Interpret and communicate clinical study data, including efficacy, safety, and patient outcomes. Collaborate with cross-functional teams across clinical, regulatory, biostatistics, research, and medical affairs. Build and maintain strong relationships with external scientific leaders, investigators, and key opinion leaders. Skills & Experience Required MD (or equivalent) with board certification or eligibility in Medical Oncology, Hematology, Radiation Oncology, or Internal Medicine with relevant oncology experience. Experience in pharmaceutical, biotechnology, or clinical research environments. Strong understanding of the clinical drug development process and execution of clinical trials. Demonstrated experience reviewing and interpreting clinical data to inform development decisions. Knowledge of regulatory requirements and Good Clinical Practice (GCP). Strong scientific communication, stakeholder engagement, and cross-functional leadership skills. Preferred Qualifications Advanced degree such as PhD, MBA, or MPH. Experience leading oncology clinical development programmes and clinical trial strategy. Track record of scientific publications, research leadership, or recognised clinical expertise. Strong knowledge of evolving oncology treatment landscapes, clinical practice trends, and competitive developments. To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed) PAYE also possible - please enquire for more information Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

Trainee Medical Reviewer Location: Berkshire (hybrid working model - at least 3 days on site) Duration: 12 months About the Role SRG are working exclusively with a top pharmaceutical company on an excellent role for aspiring Medical Affairs professionals. We are seeking a Trainee Medical Review Advisor to support the review and approval of promotional and non-promotional healthcare materials across a range of therapeutic areas. This role offers an excellent opportunity for a pharmacy or medical graduate to develop expertise in medical review, compliance, and healthcare communications, while working closely with cross-functional teams in a regulated environment. Key Responsibilities Support the review and approval of promotional and non-promotional materials to ensure compliance with relevant industry regulations and codes of practice. Provide scientific and compliance support to brand and cross-functional teams across multiple therapeutic areas. Contribute to the development and implementation of compliant processes and standards for healthcare communications and activities. Help deliver practical, compliant solutions that support business objectives, product launches, and marketing initiatives. Review materials accurately and efficiently to meet business timelines and quality standards. Participate in medical review projects and continuous improvement initiatives to enhance ways of working and best practices. Skills & Experience Required Pharmacy or Medical degree (essential). GPhC registration for pharmacists or GMC registration for physicians (essential) Strong ability to analyse, interpret, and communicate complex scientific, pharmacological, or medical information. Excellent attention to detail and commitment to accuracy. Ability to work effectively in a fast-paced, deadline-driven environment. Strong problem-solving skills with the ability to identify issues and develop practical solutions. Experience working within cross-functional teams is desirable. What We're Looking For A keen interest in medical affairs, healthcare compliance, and medical review. Motivation to develop towards Medical Signatory status. Strong communication and stakeholder management skills. A collaborative approach and willingness to learn in a highly regulated environment. To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed) Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.

BMS Engineer ROLE: BMS Engineer PAY RATE: 27.26 per hour PAYE CONTRACT TYPE: 3 Months contract - Potential for a permanent position for the right candidate LOCATION: Bristol ,BS32 About the Role We are looking for an experienced and reliable BMS Engineer to join the team. You'll be responsible for maintaining, servicing, and fault finding on Building Management Systems across a range of commercial sites. This is a field-based role, mainly covering the Bristol area, with occasional travel to Newport, Cardiff, Taunton, Swindon, Oxford, Cheltenham, Gloucester, and Hereford. What You'll Be Doing Carrying out planned preventative maintenance (PPM) and reactive maintenance on BMS systems. Diagnosing and repairing faults on Building Management Systems and associated controls. Commissioning, testing, and optimising BMS systems to ensure they are operating efficiently. Making minor software and control strategy adjustments where required. Completing service reports and keeping accurate maintenance records. Ensuring all work is carried out safely and in line with company procedures. Providing excellent customer service while working across multiple client sites. What We're Looking For Previous experience working as a BMS Engineer. Good knowledge of Building Management Systems and HVAC controls. Strong fault-finding and problem-solving skills. Able to work independently and manage your own workload. Good communication and customer service skills. Full UK Driving Licence (essential). Working Hours Flexible working between 7:00am and 7:00pm , Monday to Friday. Occasional evening or weekend work may be required. Overtime or flexible hours available for out-of-hours work. Benefit Temp-to-perm opportunity. Uniform provided. Electric company vehicle provided. Employee Benefits Programme with retail and lifestyle discounts. Employee Assistance Programme offering free support and advice. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.