Christopher Hutchinson

Drug Product Engineer (Formulation) - Ireland, Dublin - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Drug Product Engineer. What you'll do: Provide technical and compliance review and/or authorship of testing protocols, reports, and applicable manufacturing SOPs.Generate and execute documentation for cGMP activities including risk assessments /reports. Management of Equipment Vendors including execution of on-site maintenance visits, management of continuous improvement projects & spare parts criticality assessments.Support/lead maintenance of the validated state of the equipment through execution of revalidation protocols as per Site VMP. What you'll need: Extensive cGMP industrial / engineering experience, Experience in executing on the floor activities such as FAT, SAT, IQ/OQ Specific experience with Autoclave, Parts Washers, and CIP/SIP equipment. Knowledge of Formulation processes. If this role is of interest to you, please apply now!#LI-CH3

Validation Engineer - Ireland, Dublin - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Validation Engineer . What you'll do: Support the site validation activities across a number of workstreams.Develop and maintain the site Validation Master Plan.Drive development of site EMPQ strategy and implement/maintain EM protocols and procedures for graded pharmaceutical areas, ensuring compliance with regulatory guidelines.Support equipment qualification post Operational Qualification (OQ) through to Process Performance Qualification (PPQ) and subsequent revalidation.  What you'll need: Extensive direct experience with a pharmaceutical or biotechnology company with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.Bachelor’s degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry etc.Prior experience in Cleaning Validation, Temperature Mapping activities, and qualification of Parts Washers and/or Autoclaves.Experience with upstream cell culture and/or downstream formulation/fill finish processes. If this role is of interest to you, please apply now!#LI-CH3

Data Manager - Ireland, Dublin - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Data Manager. What you'll do: As a Data Manager, you will be vital in building our animal data models, working closely with Marketing, IT, and R&D leads and teams to explore the data our products upload to our data platform.You will innovate new data features and work with data scientists to create innovative farm and animal KPIs promoting animal health and well-being.You will be responsible for data quality and integrity, ensuring our data is up-to-date and of high value.Conduct data profiling, analysis, and validation to ensure the accuracy, completeness, and consistency of animal health data. What you'll need: Extensive hands-on experience working as a Data Steward, Data Manager, Data Custodian, or similar role.Experience with data management tools and technologies, such as Collibra, Immuta, and Data BricksExperience harvesting data from ERP and CRM systems such as SAP and Salesforce, with a proven track record of building complex customer data models in international corporations.Strong knowledge of veterinary medicine and animal health data management principles If this role is of interest to you, please apply now!#LI-CH3

Validation Engineer - Redmond, Seattle - 4-6 Month ContractOur client, a global biotechnology organisation, is recruiting for a Validation Engineer to join their capital project in Redmond. This new build facility will house a therapeutic protein production plant, and we are looking for a Validation Engineer to help expand our client's biotech operations throughout Europe. As the Validation Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.What you’ll do: Identify gaps, risks, and improvement opportunities, escalating issues where required.Support the maintenance of validated status through impact assessments, requalification planning, and validation updates.Maintain validation files and ensure documentation is audit-ready at all times.Participate in internal and external audits, providing subject-matter expertise on validation lifecycle and periodic review processes. What you’ll need: Experience in pharmaceutical, biotech, or other regulated GMP environments.Strong understanding of validation principles (IQ/OQ/PQ), equipment qualification, and process validation.Familiarity with regulatory guidelines including EU GMP Annex 15, FDA 21 CFR Parts 210/211, and data integrity expectations.Excellent analytical and documentation skills with a high attention to detail. If this role is of interest, please apply now!#LI-CH3

Laboratory Systems Specialist - Dublin, Ireland - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Laboratory Systems Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: The motivation to be an inspiring member of a high performing team.The desire to continuously learn, improve and develop.Be the SME on data management systems for instrument control in the laboratories, this includes but is not limited to GLIMS (Global Labware LIMS Platform), Laboratory Execution Systems (LES), Lonza MODA and Waters Empower.Work within an environment of right first time in everything that we do, through a focus on principles of lean, including simplification, standard work, visual management Desirable Experience: Degree qualification in a Technical discipline.Extensive experience in laboratory systems, Labware LIMS experience preferred.Previous experience with configuring, building, maintaining laboratory management systems such as LIMS/ MODA and /or Empower systems and interest in coding/ script.Ability to think logically and be proactive under pressure. If this role is of interest to you, please apply now!#LI-CH3

CSV Engineer - Automation/Compliance - Ireland, Carlow - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a CSV Engineer. What you'll do: Ensure compliance with Global SDLC/CSV and IT Security policies and proceduresEnsure supply of all compliance components required to deliver high quality product through tactical planning and execution of project and compliance deliverables.Participate and Comply with the MMD Quality Management System (QMS) requirements, including Chapter 14 (Computer Systems) and EU Annex 11, 21 CFR Part 11, MHRA (UK) GMP Data Integrity guidelines, Sarbanes-Oxley (SOX) regulations. What you'll need: Ability to participate in highly effective teams.Ability to work with all levels of business customers in a highly dynamic environment.Degree qualification (Science, Engineering, Technical).Extensive GxP experience in Computer System Validation (life science, pharma, medical devices) If this role is of interest to you, please apply now!#LI-CH3

Laboratory Systems Specialist - Ireland, Dublin - 22 Month Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Laboratory Systems Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: Be the SME on data management systems for instrument control in the laboratories, this includes but is not limited to GLIMS (Global Labware LIMS Platform), Laboratory Execution Systems (LES), Lonza MODA and Waters Empower.Work within an environment of right first time in everything that we do, through a focus on principles of lean, including simplification, standard work, visual managementBuild the Lab IT Systems to support Tech Transfer/Commercialisation of the biologics pipelineAn understanding in analytical methodology (e.g. HPLC, ELISA, SDS-Page, Glyco analytic, Bioassays, PCR, capillary electrophoresis, compendial assays). Desirable Experience: Degree qualification in a technical discipline.Requires extensive experience in laboratory systems, Labware LIMS experience preferred.Previous experience with configuring, building, maintaining laboratory management systems such as LIMS/ MODA and /or Empower systems and interest in coding/ script. If this role is of interest to you, please apply now!#LI-CH3

Project Engineer - Ireland, Dublin - 12 Months Initial ContractOur client, a globally recognised pioneer in Biotechnology, are recruiting for the position of a Project Engineer. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join them on their global mission to better the lives of those effected by disease and illness. What you'll do: Coordinate day-to-day activities and ensure daily and weekly deliverables are metManage various vendors and subcontractors through project deliveryAct as the client representative during daily meetingsProvide project updates to senior leadership What you'll need: Extensive engineering experience within a pharmaceutical / biotech industry.Major Capital Project ExperienceProject coordination experienceRelevant degree If this role is of interest, please apply now! #LI-CH3

Business Insights Analyst - London (hybrid) - 11 Month Contract Do you want to be involved with one of Europe’s most exciting bio-pharmaceutical manufacturers? Based in their central London offices, this is an opportunity to support Business Intelligence projects to enhance decision making for a major biotech client.This is a truly exciting project, supporting the production of lifesaving biologics-based medicines. This is a hybrid position, 2 days per week in London.What you'll do: Analysing brand and franchise performance to identify risks, opportunities, and growth levers.Translating performance data into strategic narratives that influence commercial planning.Evaluating omni-channel effectiveness and customer journey metrics to uncover behavioural drivers and friction points, informing future campaign and channel strategy and measurable improvements in customer engagement and experience.Embedding tools to support integrated performance tracking, execution visibility, and alignment across teams. What you'll need: Pharmaceutical, biotech, or medical field experience.Familiar with Veeva Customer Relationship Management (CRM), Salesforce Marketing Cloud, Veeva PromoMats.Market research understanding, including knowledge of market research techniques and guidelines.Knowledge of data sources, guidelines, statistical techniques, and digital tracking tools (Hotjar, Google Analytics).Familiar with Veeva Customer Relationship Management (CRM), Salesforce Marketing Cloud, Veeva PromoMats.Understanding of backend analytics infrastructure and visualization tools like Spotfire/Power BI. If this role is of interest to you, please apply now!#LI-CH3