Medical Advisor

Project Engineer - Dublin, Ireland - 11 Month ContractOur client is one of the world’s largest pharmaceutical organisations. With continued organisational growth including ongoing investment across the portfolio and capital projects programme at their manufacturing facility in Dublin, an excellent opportunity has arisen for a Project Engineer to join the team.Essential Duties and Responsibilities for this role include, but are not limited to, the following: Initial scope of work for this Project Engineer will be to deliver several investment projects on site with specific focus on HVAC heat recovery system, Heat pump(s), chillers etc.The Project Engineer will liaise, where necessary, with external engineering companies to complete design and execution.Maintain strict budgetary control, while adhering to agreed schedules.Manage procurement activities associated with projects, inclusive of tendering, Purchasing and Invoice management.Lead cross functional teams in development and execution of projects. Desirable Experience includes: Extensive experience in pharmaceutical project / program management.A 3rd level degree in Mechanical Engineering, or equivalent is required.Excellent project management skills, Project Management Professional (PMP) or equivalent PM qualification is a plus.Ability to plan workload and work to tight taked.Ability to communicate with Site Management, all Engineering disciplines, EHS, Production, and Quality personnel. For more information on this position, please apply with a copy of your CV today! #LI-CB1

QA Specialist - Dublin, Ireland - 12 Month Initial ContractOne of the top 10 best companies to work in Ireland is looking for a QA Specialist for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology. What you’ll do: Establishing best practices and continuous improvement initiatives, in collaboration with Quality Systems.Ensure compliance of all QC activities to all applicable policies, directives, guidance documents and regulatory requirements.Supporting the QC laboratory through global regulatory agency inspections and achievement of market approvals.Supporting the execution of the internal audit program.Supporting QC and QA Network Harmonisation initiatives. What you’ll need: BSc in Science or related discipline.Extensive Quality experience in the biopharmaceutical industry.A thorough understanding of cGMP requirements for laboratory compliance including equipment and instrumentation qualification requirements is essential.Excellent written and verbal communication skillsAbility to work on his/her own initiative in addition to working as part of a team If this role is of interest, please apply now!#LI-JS4

Clean Room SME - Raleigh, NC - 12 Month Initial ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Clean Room SME for their Raleigh, North Carolina based location.   What you'll do: Assist EPCM Team with the planning, design review, and implementation of clean room environments in alignment with ISO 14644 standards and GMP/cGMP requirements.Ensure clean room layouts, finishes, airflow, and pressure differentials meet regulatory and operational specifications.Collaborate with engineering and construction teams to ensure design intent is maintained throughout the build process.Oversee the construction and installation of clean room components including walls, ceilings, flooring, HVAC systems, HEPA filters, and pass-throughs.Conduct inspections and audits to verify compliance with clean room construction standards and protocols. What you'll need: Bachelor’s degree in Engineering, Construction Management, Microbiology, Industrial Hygiene, or a related field.Extensive experience in clean room design, construction, and validation within pharmaceutical or life sciences environments.Proven expertise in ISO 14644 standards, GMP/cGMP regulations, and contamination control.Experience leading clean room projects from concept through commissioning.Strong understanding of HVAC systems, airflow dynamics, and pressure balancing in controlled environments. If this role is of interest to you, please apply now!#LI-MC1

Construction Support Engineer - Raleigh, NC - 12 Month Initial ContractDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Construction Support Engineer for their Raleigh based location.  What you'll do: Support the installation of pharmaceutical clean utility systems, including but not limited to WFI, clean steam, and clean gases.Act as the client's agent to review and approve submittals from the Design/Builder for applicable utilities and equipment designs.Participate in constructability reviews with site construction team.Review and comment on applicable detailed design and installation specifications.Drive progress and coordination to ensure schedule, cost and quality targets are met. What you'll need: Extensive experience in the construction and commissioning of utility systems in pharmaceutical or biotech facilities.Familiarity with GMP standards, regulatory guidelines, and industry best practices.Proven ability to lead and manage construction activities within a regulated environment.Excellent problem-solving, communication, and organizational skills.Ability to read and interpret engineering drawings, P&IDs, and technical specifications. If this role is of interest to you, please apply now!#LI-MC1

Reassembly / Process Equipment Engineer - Raleigh, NC - 12 Month InitialDo you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Process Equipment Engineer for their Raleigh, North Carolina based location.   What you'll do: Provide day-to-day direction, guidance, and mentorship to technicians and contractors performing installation work.Review and interpret P&IDs, layout drawings, isometrics, and vendor documentation to ensure accurate installation.Coordinate closely with Engineering, Construction, Commissioning, and Validation teams to support system turnover and startup.Ensure all installation activities comply with GMP, safety, quality, and ASME BPE standards.Lead system walkdowns, punch list development and closure, and installation readiness reviews. What you'll need: Extensive experience in biopharmaceutical or pharmaceutical manufacturing, capital projects, or facility builds.Extensive hands-on experience with process equipment reassembly and large skid-mounted systems.Demonstrated leadership experience guiding technicians, contractors, or field teams.Strong knowledge of GMP manufacturing environments and regulated installation practices.Advanced ability to read and interpret P&IDs, isometrics, and equipment drawings. If this role is of interest to you, please apply now!#LI-MC1

E&I SME - Belgium, Brussels - 6 Month ContractWe are looking for an experienced E&I SME for a fantastic 6 month contract based in Brussels. You will be working with our client who are a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease. This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first. What you’ll do: Expert in its area of expertiseAuthor of specifications, calculation and drawings related with its area of expertiseSPOC for the contractors selected to build the installation in its fieldBe the package owner to manage the contract : planning, budget, quality of realisation What you’ll  need: Proven experience in CAPEX projectExtensive experience in the engineering for industrial and/or pharmaceutical environmentExperience of biotech environment in the bio-pharmaceutical industry is preferred.Knowledge of safety, GMP and environmental regulatory requirements.Experience in legal conformity and energising process (3 green lights) If this role is of interest to you, please apply now! #LI-CB1

Project Engineer - Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Project Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.What you’ll do: Accountable for meeting key project deliverables for safety, financial management, schedule management and scope management across these projects.Accountable for ensuring projects are compliant with good engineering practices, company policies, regulations and codes.Liaise with Global Engineering/Global EHS/Global Procurement to ensure all are aligned and support project deliverables.Accountable for strict adherence to project stage-gate principles for managing the life-cycle of projects. What you’ll need: A degree in an engineering discipline preferred.Extensive project engineer/manager experience across the project life cycle within a pharmaceutical environment.Demonstrable skills that can be applied to effectively manage and execute projects from initiation to completionDemonstrable skills and competencies that will enable the successful candidate to be able to manage a diverse team of engineering professionals/contractors etc. to deliver projects safely, on time and within budget. If this role is of interest, please apply now!#LI-JM3

Supply Chain Business Analyst - Edinburgh, UK - 12 month initial contractOur client, a global Contract Development and Manufacturing Organisation, specialising in cell and gene therapies, are seeking at Supply Chain Business Analyst. The client is a leader in iPSC and advanced therapy platforms, supporting partners from early development through clinical and commercial production. With facilities in the UK and US, the client combines cutting‑edge science, rigorous quality, and a collaborative approach to accelerate life‑changing therapies to patients.What you'll do: Support focused business processes improvements and digital transformation to maximise system utilisation and process efficiency.Ensure all business change activities are undertaken in a planned, controlled and sensitive manner.Deliver efficiency and quality benefits to the business.Effective Business Change Management including associated documentation changes and resource training.Development and tracking of KPI’s and other associated metrics to demonstrate both quality and business benefits. What you'll need: Formal methods of process documentation including TOM & Use Cases.Process analysis and development of detailed process flows in a complex GMP manufacturing environment.Experienced in a broad range of Supply Chain and ERP related processes (Purchase to Pay, Inspect to Release, Plan to Produce, and including “outliers” in a GMP environment.Excellent project management skills.An understanding of the Software and System Lifecycles including Waterfall, V-Model and Agile. If you would like to apply or find out more, get in touch now!#LI-RW1

Senior Construction Manager - Copenhagen, Denmark - 12 months initial contractOur client, a global pharmaceutical company, are looking for a Senior Construction Manager to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems. What you'll do: Provide leadership, governance, and oversight as Senior Construction Manager on the client side for a large scale (circa €1bn) package within a larger overall capital program.Drive EPCM performance, ensure safe, compliant delivery.Establish and run client-side governance (stage gates, steering committees, monthly/quarterly reviews).Own KPIs/dashboards (cost, schedule, quality, HSE-leading indicators, change volume, claims status, readiness).Engage executive stakeholders (VPs/Project Directors, Finance, Ops, QA/Validation, EHS) to secure timely decisions on scope changes, resequencing, claims, and critical risks. What you'll need: Previous experience of managing large construction projects (500mn )Client side and engagement with senior level stakeholdersProven ownership of large single construction packagesAccountability across budgets, schedules, quality, safety, contract administrationRisk mitigation If you would like to apply or find out more, get in touch now!#LI-HS1