Teanne Luck

Finance Assistant

I joined QCS Staffing in May 2023 as a Pay & Bill Assistant. I have previously worked in the care industry and have experience in a contract administrator role, but this is my first time working within recruitment.

Outside of work I like to travel to anywhere where the sun is. I enjoy watching or playing sports, mainly football, and socialising with friends and family (Normally with a glass of wine at the pub).

View our latest jobs

Data Manager

ContractDublin, County Dublin, Ireland

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

Operational Readiness PM

ContractOhio, United States

Operational Readiness PM - US, Ohio - 12 Month ContractBe part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Ohio, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for an Operational Readiness Project Manager to join the team and help deliver this world-class program. What you’ll do: Own and lead operational readiness planning and execution for assigned areas of the Medicine Foundry.Partner with Manufacturing, Quality, Engineering, Validation, Supply Chain, EHS, IT, and other site functions to define readiness scope and deliverables.Translate operational readiness requirements into structured, executable plans and schedules.Build, manage, and maintain operational readiness schedules aligned with construction, commissioning, and qualification milestones. What you’ll need: Bachelor’s degree in Engineering, Chemistry, or related scientific/technical discipline.Extensive experience in pharmaceutical or biotech manufacturing environments.Direct experience supporting operational readiness, startup, or commissioning of a new or expanded manufacturing facility.Strong understanding of manufacturing operations and how key site functions interact (Operations, Quality, Engineering, Validation, Supply Chain). Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Senior Project Manager

ContractSurrey, South East, England

Senior Project Manager - UK, Surrey - 12 Month ContractWe are looking for an experienced Senior Project Manager for a fantastic 12 month contract based in Surrey.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: Lead the programme from initial definition through planning, delivery, commissioning, and handover.Hold accountability for final engineering aspects, ensuring design intent, technical standards, safety requirements, and compliance obligations are met.Understand and oversee the full commissioning process for R&D and laboratory environments, ensuring readiness for functional testing, validation, and operational ramp-up.Develop and maintain integrated programme schedules, resource plans, and performance baselines. What you’ll  need: Extensive experience managing major capital programmes, ideally within R&D, laboratories, scientific facilities, pharma, defence, advanced engineering, or highly regulated technical environments.Strong understanding of engineering processes, design assurance, and technical governance.Demonstrable exposure to commissioning activities within complex facilities.Proven ability to lead multidisciplinary teams through full lifecycle delivery If this role is of interest to you, please apply now!#LI-TN1

Tech Transfer Engineer

ContractDublin, County Dublin, Ireland

Tech Transfer Engineer (Downstream) - Ireland, Dublin - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Tech Transfer 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: Deliver tech transfer readiness activities from facility assessment through to PPQ execution and report completion for a new product introduction to the MPCC Cruiserath.Authoring of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process.Identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools.Generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scaleProvide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution What you’ll need: Minimum BSc or equivalent extensive experience in drug substance manufacturing technical support in the biopharmaceutical industry including tech transfer preparation, execution and post-execution activities.You have demonstrated awareness of cGMP compliance and regulatory agency requirements as well as strong oral communication and technical writing skills.Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organisation, and in local group settings.Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form. If this role is of interest, please apply now!#LI-JS4

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