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27,000 per annum 12‑Month Fixed‑Term Contract Location: Midlothian Blue Arrow Recruitment is delighted to be working with a global organisation to recruit a Materials & Distribution Officer on a 12‑month fixed‑term contract. This is an excellent opportunity for someone looking to gain or build experience within a regulated warehousing and distribution environment, supporting the global distribution of medical products. The Role Operating as part of a service‑focused warehouse team, you will support day‑to‑day warehouse and inventory activities, ensuring materials and finished goods are received, stored, picked, packed and dispatched accurately and in line with GMP and GDP standards. Key Responsibilities • Receiving and booking materials into the onsite inventory management system (TROPOS), • Picking, packing and dispatching finished goods for external customers, • Distributing materials to internal customers via a warehouse ticketing system, • Maintaining accurate inventory levels and records, • Supporting stock checks, replenishment, FEFO processes and material disposal, • Ensuring full compliance with GMP, GDP, Health & Safety and regulatory requirements, • Maintaining accurate documentation and system records, • Participating in training and continuous development activities, • Supporting general warehouse operations as required What We're Looking For • Good IT skills, including Microsoft Outlook, Word and Excel, • Strong organisational and time‑management skills, • Ability to work both independently and as part of a team, • Previous warehousing experience, • Exposure to GMP or GDP regulated environments, • Experience using inventory management systems Additional Information • Salary: 27,000 per annum, • Contract: 12‑month fixed‑term contract with our client, • Hours: Standard working hours, with occasional overtime desirable, • Location: Edinburgh area Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.

Actuarial Manager | DB Consolidation | Up to £80k Location: UK-wide hybrid, Manchester, Edinburgh, Glasgow, Leeds, London. Other office locations will be considered. Package: checker, Up to £80,000 base + bonus | doer, £45,000-65,000 base + bonus Traditional DB pension management is often slow and bogged down by governance. This role sits within a team at the forefront of Operational Consolidation, providing a "one-stop-shop" solution that replaces traditional, inefficient models. Using their award-winning Pension Platform, this team manage over 65 schemes collectively. By bringing administration, actuarial, and investment services under one roof, they can provide "big scheme" service and £1bn+ investment buying power to schemes of all sizes. The Team: • No More "Boring" Admin: Through a partnership with professional trustees, admin is automated, so you can focus on technical calculations and strategic advice, not secretarial tasks., • Market-Leading Growth: With 65+ schemes already on the platform and £3bn in assets, you’re joining a growing DB Master Trust / Consolidator of the Year., • End-to-End Ownership: You won’t just see fragments of a scheme. You build the models, you run the numbers, and you see the direct impact on the scheme's endgame. The role: • Heavy involvement in "endgame" planning, including scheme buy-outs, GMP equalisation, and benefit rectification, • Take ownership of a portfolio of schemes, direct ownership of client communications and attend meetings as you progress, • Responsibility for valuations, member benefit calculations, funding updates, and accounting disclosures, • Performing and checking pension liability calculations, • Manage workflow and mentor junior colleagues The Individual: • FIA: Nearly/ Newly qualified Actuary, 4-10 years total experience, • Must have experience in a Pensions Actuarial role within a UK-based consultancy, • Technical understanding of how calculations work, not just how to populate models, • Appetite to take responsibility and organise your own portfolio This team offer clear promotion pathways based on capability and contribution, and full ownership of schemes and end‑to‑end work, unlike competitors. Open to part-time and full-time. Please apply here, or get in touch. It is best to separately email your CV directly to me. Yasmin Andrews Life & Pensions Actuarial Hiring Lead, Principal Consultant Get in touch to discuss the market. A range of seniorities and specialisms covered: M: 07458161817 E:

Project Manager - Diagnostics Hartmann Young is partnered with a global medical diagnostics company specialising in IVD that target autoimmune disease, allergy testing and transfusion medicine. They are going through a phase of expansion and are looking to grow their team in Edinburgh, UK, with the addition of a Project Manager. The Role: • Lead and coordinate the design, planning, and execution of assigned projects., • Manage cross-functional project teams within a matrix environment., • Organise and chair project meetings to ensure delivery milestones are met., • Manage external suppliers and partners to ensure successful delivery of project objectives., • Collaborate with Project Sponsors, Technical Leads, and team members to deliver projects in line with agreed plans., • Ensure all project activities and outputs comply with internal design control and project management procedures., • Communicate project goals, timelines, and progress effectively to stakeholders at all levels., • Identify, assess, and manage project risks, issues, and changes, implementing appropriate mitigation strategies., • Assist in training and mentoring staff in project management tools and methodologies., • Ensure all activities are conducted in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP), and relevant regulatory requirements., • Undertake additional duties as required. The Person: • Bachelor’s degree in a scientific discipline or equivalent experience., • Proven project management experience, including managing multiple projects simultaneously., • Professional certification (e.g. PMP, PRINCE2, or equivalent) (Desirable), • Experience within regulated industries (e.g. medical devices, life sciences)., • Knowledge of IVDR or regulatory-focused projects. (Desirable), • Familiarity with ISO 13485 and/or relevant FDA regulations (e.g. CFR 820). (Desirable), • Understanding of design controls and regulatory submission processes (e.g. CE marking or FDA submissions). (Desirable)

Production Scientist - Diagnostics Hartmann Young is partnered with a global medical diagnostics company specialising in IVD that target autoimmune disease, allergy testing and transfusion medicine. They are going through a phase of expansion and are looking to grow their team in Edinburgh, UK, with the addition of a Production Scientist. The Role: • Provide technical and scientific guidance to operational teams, including support with troubleshooting and customer complaint investigations., • Conduct technical reviews and contribute subject matter expertise to problem-solving activities., • Monitor and trend departmental outputs, identifying areas for improvement and implementing corrective actions., • Support development initiatives and projects by providing technical input and guidance., • Ensure team members maintain a strong understanding of products, processes, and quality requirements., • Contribute to the development and maintenance of risk documentation and departmental procedures., • Oversee training programmes and competency assessments to ensure staff are appropriately skilled and compliant., • Deputise for the Manufacturing Team Leader when required., • Represent the department at cross-functional meetings and communicate key updates to the wider team., • Ensure adherence to manufacturing processes and regulatory standards at all times., • Collaborate with procurement to maintain appropriate stock levels of critical materials., • Maintain audit readiness across all departmental areas., • Ensure compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP), and relevant regulatory requirements., • Monitor departmental performance against objectives, escalating issues and driving improvements., • Ensure compliance with COSHH requirements, including timely risk assessments., • Ensure equipment is maintained and documented in accordance with procedures., • Participate in continuous improvement initiatives, including 5S and Six Sigma activities., • Support the review and update of SOPs and related documentation., • Manage quality records (e.g. CAPAs, non-conformances, change controls) within agreed timelines., • Undertake additional duties as required The Person: • Relevant scientific degree., • Experience working in a scientific laboratory or regulated manufacturing environment., • Strong understanding of GMP and GDP requirements., • Experience working with biological materials would be desirable. If this sounds like an opportunity of interest, please reach out or apply directly below - We'd love to hear from you! Due to the high volume of applications, we cannot guarantee a response with tailored feedback.

SRG are delighted to be partnered with a world-leading cell and gene therapy manufacturing organisation based in Edinburgh as they continue their exciting expansion programme. As part of this expansion this company are seeking a shift-based Senior QC Analyst with an analytical background to join their team on a full-time, permanent basis. The Role As Senior Quality Control analyst you will join a large, highly experienced quality function to test clinical and commercial cell and gene therapy projects/products. You will be a key point of contact for a variety of QC assays with a particular focus on flow cytometry. As this is a senior position you will be responsible for leading the analytical quality control team on a shift, being a go-to person for technical queries related to the workflow and general GMP enquiries. As well as being a key figure in the QC team you will collaborate closely with manufacturing/production to ensure GMP method transfer and compliance. The Right Person • Demonstrable prior experience in a GMP quality control lab environment, • Team leadership experience, • Expert level practical knowledge of flow cytometry, • Experience in assay validation, • Prior experience in a cell and gene therapy manufacturing organisation

£27,000 per annum\n\n12‑Month Fixed‑Term Contract\n\nLocation: Midlothian \n\nBlue Arrow Recruitment is delighted to be working with a global organisation to recruit a Materials & Distribution Officer on a 12‑month fixed‑term contract.\n\nThis is an excellent opportunity for someone looking to gain or build experience within a regulated warehousing and distribution environment, supporting the global distribution of medical products.\n\nThe Role\n\nOperating as part of a service‑focused warehouse team, you will support day‑to‑day warehouse and inventory activities, ensuring materials and finished goods are received, stored, picked, packed and dispatched accurately and in line with GMP and GDP standards.\n\nKey Responsibilities\n\nReceiving and booking materials into the onsite inventory management system (TROPOS)\nPicking, packing and dispatching finished goods for external customers\nDistributing materials to internal customers via a warehouse ticketing system\nMaintaining accurate inventory levels and records\nSupporting stock checks, replenishment, FEFO processes and material disposal\nEnsuring full compliance with GMP, GDP, Health & Safety and regulatory requirements\nMaintaining accurate documentation and system records\nParticipating in training and continuous development activities\nSupporting general warehouse operations as required\n\nWhat We're Looking For\n\nGood IT skills, including Microsoft Outlook, Word and Excel\nStrong organisational and time‑management skills\nAbility to work both independently and as part of a team\nStrong attention to detail and commitment to compliance and qualityDesirable (but not essential):\n\nPrevious warehousing experience\nExposure to GMP or GDP regulated environments\nExperience using inventory management systems\nForklift or driving licence (not essential)Full training will be provided for the right candidate.\n\nAdditional Information\n\nSalary: £27,000 per annum\nContract: 12‑month fixed‑term contract with our client\nHours: Standard working hours, with occasional overtime desirable\nLocation: Edinburgh area \n\nBlue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people

With a commitment to scientific excellence, Moredun Scientific provides high-quality services to meet the needs of clients worldwide. Moredun Scientific is a GLP/GMP-accredited contract research organization offering research and testing services to the animal health, pharmaceutical, and biotechnolo

Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified actuaries to a vital role that not only drives revenue but also fosters professional growth a

RoslinCT in Edinburgh BioQuarter is looking for a Quality Investigator I to conduct thorough investigations of non-compliances in a GMP environment.

A leading cell and gene therapy organization is seeking a Senior QC Analyst to join their Quality team in Edinburgh. The role involves working on analytical assays for human therapies, leading process improvements, and ensuring compliance with GMP standards.

This role involves installing, maintaining, and qualifying laboratory instruments while ensuring compliance with cGMP and regulatory standards.

The role involves leading complex calculations and collaborating on various pension projects that drive improvement and support junior colleagues. The ideal candidate is a qualified actuary with strong analytical skills and experience in UK pension schemes, making this a fantastic opportunity for ca

Actuarial Consultant - GMP Equalisation and Project Work (Nationwide). Take charge of checking and reviewing complex calculations, ensuring accuracy and clarity in communicating results to consultants and wider support teams. Previous experience in a similar role within an Actuarial team, particular

A leading Scottish law firm is seeking a Specialist Pensions Lawyer to join their Pensions team.This role is available at Director or Senior Associate/Associate level and supports remote/hybrid working options.The ideal candidate has 5-10 years of experience in pensions law, with knowledge of DB sch

National African-American Insurance Association (NAAIA) is seeking a talented Actuarial Consultant in Edinburgh to join their team.

This position involves supporting daily warehouse activities, ensuring that materials and finished goods are accurately received, stored, and dispatched in compliance with GMP and GDP standards.

This role is primarily based in our Edinburgh BioQuarter site however there may be a requirement to travel to our BioStore site in Livingston.We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people�

The ideal candidate has a relevant scientific degree and experience in a scientific or regulated environment, along with a strong understanding of GMP and GDP.

This full-time role requires compliance with GMP and regulatory standards while performing packing activities. Candidates should have Standard Grade in Mathematics and English (or equivalent), and experience in a GMP environment is a plus.

Ipsen Group recherche un Logistics Operator pour son site de Wrexham.Ce rôle crucial soutient les opérations d'entrepôt en garantissant que les matériaux sont reçus, stockés, déplacés et émis efficacement.Avec une attention particulière à la précision et à la sécurité, vous contribuer

Cpl Life Sciences is looking for a Quality Operations Associate in the United Kingdom to support Quality Systems and Assurance in a pharmaceutical setting.The role includes maintaining the Quality Management System and participating in audits.Candidates should have a bachelor's degree in life scienc

NHS Blood and Transplant is seeking an Eye Services Technical Officer to support our Eye Bank team in maintaining high-quality services.This role includes preparing samples, maintaining equipment, and ensuring compliance with standards.The position offers a supportive work environment, flexible work

Deze rol vereist minimaal 2 jaar labervaring, een MLO opleiding, en kennis van GMP/GcLP.

AliveDx is seeking a Production Operator for their Manufacturing team near Edinburgh.In this full-time, temporary role, you will ensure the quality of diagnostic reagents and maintain equipment while participating in continuous improvement.The position offers a salary of £26,500 along with 25 days

The GMP Production Manager will be responsible for establishing the GMP production team and taking a lead role in the operation of the GMP production suites. The GMP Production Manager will lead and develop the GMP production team and will be responsible for leading the day-to-day management, operat

The role involves running the packaging line, ensuring compliance with GMP, and maintaining quality standards while packaging pharmaceuticals.

SRG is seeking a Project Lead in Scotland to oversee batches manufactured in cleanrooms within their GMP production team. Candidates should have a degree in a scientific discipline and experience in a cGMP pharmaceutical environment, coupled with skills in time management, problem-solving, and profi

Deep GMP experience not essential (you will be trained) but previous experience in GMP calculations at some level is. Technical GMP Actuary or Specialist (Pensions). A great opportunity for a technical pensions actuary or GMP specialist.

A leading consultancy in the United Kingdom seeks a qualified or part qualified Actuary to provide advice on GMP equalisation and benefit rectification projects.

Reacta Healthcare Limited is seeking a Production Operator to work within their manufacturing facility in the United Kingdom.The primary role involves facilitating activities in preparation, manufacturing, and cleaning to support the production process, ensuring compliance with Good Manufacturing Pr

A leading pharmaceutical company in the United Kingdom is looking for a Maintenance Technician to provide technical maintenance support within its vaccine manufacturing facilities in Milton Keynes.The role requires expertise in mechanical and electrical systems, with responsibilities including execu

A minimum of 3 years' experience within a pharmaceutical environment is required, along with a strong understanding of GMP/GDP regulations.

This role sits within their GMP production team and is accountable for the oversight of batches manufactured in cleanrooms, supporting the delivery of manufacturing projects to agreed timelines, quality standards and budgets. Experience in a cGMP pharmaceutical manufacturing environment.

A leading pharmaceutical company in the United Kingdom is seeking a highly motivated Manufacturing Technician.This role entails operating and maintaining manufacturing equipment, ensuring adherence to safety and quality standards, and supporting production efficiency.Candidates should have a High Sc

You will ensure project delivery from technology transfer to GMP manufacturing while managing risks and maintaining strong client relationships.

A leading pharmaceutical manufacturer in the UK seeks a Multi Skilled Engineer.This permanent position involves supporting the maintenance team with breakdowns and scheduled activities.Ideal candidates will have a minimum City & Guilds qualification with significant maintenance engineering experienc

A global pharmaceutical company in the UK is seeking a Senior Virus Seed Technician to support the production of virus seeds for Foot & Mouth Disease antigen manufacturing.The role includes managing production activities, maintaining compliance with established standards, and coordinating stock move

A leading cell and gene therapy company in the United Kingdom seeks a Senior Validation Officer to manage validation activities within a GMP environment.

Responsibilities include maintaining hygiene, undertaking routine cleaning tasks, and adhering to GMP standards.

American Health Packaging in the United Kingdom seeks dedicated team members to join Cencora, a global pharmaceutical solutions company.The role involves ensuring compliance with company procedures and Health & Safety standards while performing operational duties.Candidates must report any issues re

Candidates will need a foundational understanding of GDP and GMP, as well as the ability to foster operational improvements.

We are currently seeking a Care Home Operations Manager to join our team and support homes across our North Division.As a Care Home Operations Manager at Barchester, you will travel across and support your patch to help us deliver the high standards we're known for, as well as provide inspirational

Due to our continued growth, we now have an exciting opportunity for a part-time Cleaner to join our business working in a retail environment in Edinburgh.Experience is preferred but not essential as we will invest in your training and development, while giving access to education opportunities for

We are representing a prestigious global management consultancy looking for a Senior Operations Manager to join their internal teams and run the ops for their Design Centre of Excellence (CoE).This is an interim requirement supporting maternity cover.You will partner directly with senior leadership

Sapiens is hiring a Manager, Channel Enablement & Certification - a key global role for a natural orchestrator who loves empowering partners to succeed.In this high‑impact position, you’ll design and deliver scalable enablement and certification programs that elevate the capability, confidence,

Are you ready to take command of a high-performing service desk operation, lead exceptional teams, and set the gold standard for MSP Service Operations?.This role calls for a decisive, driven, and deeply experienced Service Operations Manager to take ownership of ROCK’s frontline service capabilit

Business Manager - Finance & Commercial Operations.Wilkinson & Associates is delighted to be exclusively engaged on behalf of a highly regarded Edinburgh-based professional services business to appoint a Finance & Commercial Operations Manager.This is a rare opportunity to join an established boutiq

We're looking for a reliable and proactive.Working under the direct supervision of the Cleaning Supervisor, you'll also liaise with site management to ensure consistently high standards are maintained across the building.On site at a development in Harrow (HA0) - 15 hours per week - working Saturd