Quality Assurance Specialist/QP

QC Material Management Analyst - Ireland, Dublin - 12 Month ContractLocated on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a QC Material Management Analyst to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow. What you’ll do: Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.Manage TempTales and shipping documents when receiving samples from external sites. What you’ll need: The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline.Extensive experience in a pharmaceutical / healthcare laboratory or related technical function. If this role is of interest, please apply now!#LI-JS4

Automation Area Lead - 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 a Automation Area Lead to join the team and help deliver this world-class program. What you’ll do: Technical ownership for an area in a projectDefine the S88 software structure and list for the areaDevelop draft function design specifications for the areaWork with system integrators to finalize the functional specificationsParticipate in P&ID and control strategy reviews What you’ll need: Key Measures of Success:Area automation deliverables consistent with program standards and philosophy.FDS and software deliverables delivered on time and to quality.Issues tracked, resolved, and documented with minimal impact to schedule. Area automation scope delivered successfully through design, FAT, SAT, and turnover. Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

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

Contracts Manager - 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 a Contracts Manager to join the team and help deliver this world-class program. What you’ll do: Lead the administration and governance of construction contracts during executionOwn the full contract lifecycle post-awardAct as the primary commercial and contractual interfaceSupport dispute resolution and claims management  What you’ll need: Extensive experience of contract management experience on large-scale CAPEX projects ($250m )Owner’s representative or EPCM delivery modelsConstruction-phase contract administration Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!#LI-AN1

Project Manager - US, North Carolina - Long Term ContractOur client, a global pharmaceutical manufacturing organization are looking for a talented Project Manager to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States. What you'll do: Lead the planning, execution, and delivery of capital projects, ensuring alignment with business objectives, schedule, and budget.Develop and manage project scopes, budgets, schedules, and risk assessments, driving accountability across teams.Coordinate with cross-functional stakeholders, including engineering, operations, quality, procurement, and regulatory teams, to ensure seamless project execution.Manage contractor and vendor relationships, overseeing procurement, contract negotiations, and project execution. What you'll need: Extensive experience in capital project management within the pharmaceutical, biotech, or life sciences industry.Proven track record of delivering complex capital projects on time and within budget.Experience managing process equipment, utilities, automation systems, and facility expansions.Strong leadership and communication skills (written and verbal), with the ability to influence, negotiate, and build relationships with stakeholders at all levels. If you are interested, please apply now for immediate consideration and further information.#LI-MC1

Automation Engineer - Ireland, Dublin - 12 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 Automation Engineer. What you'll do: Partner with local site project teams to scope changes on the PLC systemMaintain Inventory and control upgrades to PLC/SCADA systemsFollow the SDLC Procedure to implement changes (covering RS updates, RTM Change control, Implementation and test)Assist in integrating PLC/SCADA systems to core systems on the Manufacturing network including the site historian, Time server, central software repository etc. What you'll need: Experience in the commissioning of PLC/SCADA systems at a GMP manufacturing site.Experience with Siemens software including TIA Portal, WinCC, PM-Analyse, Simatic LogonExperience interfacing to control systems via common industrial protocols such as OPC UA, Profibus, Profinet, MODBUS (RTU and TCP) If this role is of interest to you, please apply now!#LI-WS1

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

Senior sales Manager – Berkhamsted, Hertfordshire – Excellent Benefits We have an amazing opportunity for a Senior sales Manager to join our team in our UK office! At QCS Staffing, we’ve been delivering expert talent solutions in five of the world’s fasted growing sectors, and sourcing candidates from all over the globe for over 33 years!  With over 150 employees across our offices in the UK, US, and Europe, we are constantly on the hunt for eager individuals to join our team. What we provide: An inclusive ‘one team’ ethos, with endless socials, charity events and celebrations!Fantastic career progression opportunities, award-winning training and development programs (we invest in YOU)Private Healthcare & Pension planEarly finish on a FridayHybrid workingEnhanced maternity and paternity pay Paid parking  What you’ll do: To proactively identify and develop new business contacts to generate requests for contractors.Build and implement detailed and effective plans to achieve sales, financial and budgetary objectives, incorporating accurate performance monitoring with regular reports and forecasts as required.Identify business objectives and critical success factors to support supervision and management of daily sales and administrative activity.Agree individual objectives with direct reports setting clear review schedules and performance guidelines. Maintaining regular monitoring of these objectives between the reporting periods.  What you’ll need: The ability to work closely with people and to be genuinely interested in their myriad ideas, problems, concerns and hopes.Ability to problem solve under considerable pressure featuresShe/he needs to be a skilled organiser who can prioritise, cope with and respond to many issues simultaneously.Strong time management/ planning skills. If you're driven, curious, and love working with incredible people - apply now and grow with us!#LI-PT1

Work Package Owner - Ireland/Remote - 12 Month ContractHow would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!Our client is currently seeking the skills of a Work Package Owner to join their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!What you'll do: Assists project manager or line manager within project leadership in planning and delivering defined work scope on a project to meet agreed schedule and budget.Coordinates with all projects related members on day-to-day progress of work activities to ensure timely completion of a project.Acts as a package lead or area lead within a project.Prepares regular project reports and presentations for key stakeholders. What you'll need: Take lead of the equipment facility fit out for our Singapore siteSupporting the detailed Design activities for DS process equipment. (Bioreactors / Chromatography Skids)The candidate should have experience of DSP in a life sciences context.The role is execution focused (as with all WPOs) rather than been a lab ‘subject matter expert’ the person needs to coordinate and drive the package forwards If this role is of interest to you, please apply now!#LI-LP1