csv engineer jobs in Limerick

Job Title: Computer System Validation (CSV) Engineer Make sure to apply with all the requested information, as laid out in the job overview below. Location: On-site (Limerick) Role Overview: The CSV Engineer will be responsible for ensuring that all computerised systems within the pharmaceutical environment are validated in compliance with industry...

Whatis it like to work at SimoTech? With a strong collaborative teamworkculture based on respect, trust, and excellence, we play a criticalpartnering role to our clients’ life-changing supply of products topatients. In return, there is excellent salary, benefits, careerprogression, educational support andmuch more.SimoTech require an DeltaV CSV Engineer to...

MES Engineer About the Role We are seeking an experienced MES Engineer to join a growing team supporting the design, implementation, and ongoing enhancement of Manufacturing Execution System (MES) solutions within a regulated manufacturing environment. This role offers the opportunity to work closely with cross-functional teams to digitalize manufacturing...

Project Delivery Partners Pte Ltd in Limerick is seeking a Computer System Validation (CSV) Engineer to ensure computerized systems in pharmaceutical environments are validated and compliant with industry regulations. If you are considering sending an application, make sure to hit the apply button below after reading through the entire description. You...

Blackfield Associates is partnering with a leading pharmaceutical manufacturer to recruit a skilled Computer System Validation (CSV) Engineer for their manufacturing operations team.You will lead and execute CSV activities for Emerson Syncade MES, ensuring GMP/GxP and 21 CFR Part 11 compliance, authoring validation documents, and collaborating with...

SimoTech in Limerick is seeking a DeltaV CSV Engineer to support a biotech manufacturing facility for a multinational biopharma client. You will validate computerised systems within the process automation framework to ensure compliance with industry standards.The ideal candidate has 5+ years’ CSV experience in pharma, hands-on DeltaV and Siemens PLC...

PACIV in Munster, Ireland, seeks an experienced Computer System Validation (CSV) Engineer for a site-based role in a multinational life sciences environment. You will lead CSV activities for digital manufacturing capital projects, ensuring systems are validated per GAMP5 and regulatory standards. Responsibilities include developing plans, reviewing SDLC...

Why SimoTech What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust, and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients.  In return, there is excellent salary, benefits, career progression, educational support and much...

Senior Computer System Validation (CSV) EngineerLocation: Limerick, Ireland Job Type: Full-Time Experience: 10+ Years Eligibility: EU Nationals PreferredRole OverviewWe are seeking an experienced Senior CSV Lead to manage validation and compliance activities for GxP-regulated computerized systems within a pharmaceutical manufacturing environment. The role...

EFOR is seeking an experienced MES Engineer to join a growing team focused on designing, implementing, and enhancing MES solutions in a regulated manufacturing setting. The role involves working with cross-functional teams to digitalize processes, improve efficiency, and support continuous improvement initiatives.Key responsibilities include transitioning to...

Westbourne IT Global Services is seeking an experienced eSystems Specialist to support implementation, administration, and continuous improvement of electronic systems in a regulated environment. You will collaborate with Quality, IT, Engineering, Validation, Manufacturing and other functions to ensure systems stay compliant and effective.You will lead...

Why SimoTech What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust, and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients.  In return, there is excellent salary, benefits, career progression, educational support and much...

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support...

Innopharma Technical Services, part of Innopharma Group, specializes in the training and employment of highly skilled, project ready, Engineers & Scientists to the (Bio) Pharmaceutical and MedTech Manufacturing Sector. Are you ready to take the next step in your career within a leading biopharma environment? We are now seeking a Computer Systems Validation...

Cognizant Life Sciences Manufacturing is seeking a DevOps Lead with a strong software engineering background to define and own our DevOps strategy, focusing initially on the Manufacturing Execution System (MES) programme and bridging development, operations, and quality in a regulated environment.You will design and maintain CI/CD pipelines, own the...

Morgan McKinley is recruiting for an Automation / Systems Engineer to support a greenfield biopharma expansion in Kerry, Ireland. The role centers on rapid implementation of a high-speed filling line, compounding rooms, and clean utilities. The position requires strong PLC/SCADA/DCS skills, OT networking, and CQV/CSV experience, with multi-year project...

Now Hiring: Software Test Lead – MES (Limerick, Ireland | Onsite) Do you see yourself as the last line of defence between a software release and the manufacturing floor? EFOR Group, a trusted Life Sciences consulting partner, is looking for an experienced Software Test Lead to own quality on a major Manufacturing Execution System (MES) programme in...

SimoTech provides manufacturing automation and IT systemsengineering, project management and validation services. We partner with lifesciences companies to design, build, operate and optimise critical processautomation systems that deliver fast track project delivery, operationalefficiency, improve manufacturing agility and achieve regulatory compliance.Why...

Lead testing and validation for MES implementation, upgrade, and integration projects in a regulated manufacturing environment.Key Responsibilities- Own testing strategy across MES projects; act as release quality gate- Guide CSV activities in line with GxP and GAMP 5- Build test documentation: plans, cases, scripts (functional, regression, integration,...

Role Overview We are looking for an experienced eSystems Specialistto support the implementation, administration, maintenance, and continuous improvement of electronic systems within a regulated environment. The successful candidate will work closely with Quality, IT, Engineering, Validation, Manufacturing, and other business functions to ensure electronic...