Jobs: biologe

Overview Are you ready to lead commissioning, qualification, and validation that brings lifesaving biologics closer to patients who need them most? Do you thrive on turning complex bioprocess systems into reliable, compliant, and inspection-ready operations? As a Senior CQV Engineer, you will be central to delivering new product introductions and continuous...

A leading Biotech Consultancy firm is seeking a Validation Specialist based in Dundalk, Ireland. The role involves supporting validation activities, developing validation plans, and overseeing EMPQ validation studies. Candidates should have 3-5 years of experience in the pharmaceutical or biotechnology sector, along with a degree in Biological Sciences or a...

Overview Ref. 1351 Validation Engineer (EMPQ) A fantastic opportunity has arisen with our client, a leading multinational pharmaceutical company, for a Validation Engineer. The successful candidate will take a lead in utilising the latest innovations in technology. The role is based at Dundalk, Co. Louth. The role involves driving the development of the...

A leading recruitment firm is seeking a Molecular Diagnostics Technical Sales Representative to enhance market presence across Ireland. The ideal candidate will have a degree in the biological sciences, proven laboratory experience, and excellent communication skills. Responsibilities include growing market share, delivering exceptional customer service, and...

The role: PE Global is currently recruiting for a Senior Validation Engineer on behalf of a leading pharmaceutical company based in Carlow. This is an initial 11-month contract role. Responsibilities: Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process. ...

Senior Project Scheduler required for a leading Biotech facility in Ringaskiddy, Cork - Initially a 12 month contract The (Sr.) Project Scheduler position within the Biologics Centre of Excellence (BCoE), Technical Development Services (TDS), is accountable for developing, monitoring, and optimizing project schedules in Microsoft Project. ROLE: The role...

Role Description Equipment Validation and sterilisation Validation Role Functions (Functions include, but are not limited to, the following) Bring energy, knowledge, innovation to carry out the following: Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process....

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in...

Sterilisation Manager Our client, a global healthcare organisation are currently recruiting for a Sterilisation Manager for their medical device manufacturing and R&D site. As Sterilisation Manager you will be responsible for leading sterilisation activities in compliance with applicable quality systems, regulatory requirements, and internal policies....

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in...

8 Months, Fixed Term Whole-Time Post Position Summary Applications are invited for the positions of Post-Doctoral Researcher in APC Microbiome Ireland. Several unfortunate biological factors must be combined in order to induce the debilitating condition that is Inflammatory bowel diseases. The microbial population resident in the mucosal layer in the gut is...

Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. This role will provide client side design input at the Basis of Design, Detailed Design, Commissioning,...

Job Specification The technical writer is responsible for the development, creation, revision and control of engineering documentation at our clients new biologics facility which is currently under construction. The successful candidate will establish key relationships across various project functions to ensure engineering documentation requirements are...

Description Key Account Manager, Oncology About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are...

Senior QC Analyst – Biochemistry (Biopharma) Join our growing biopharma team as a Senior QC Analyst, where your expertise drives our commitment to quality and innovation. What You’ll Do: Lead, support, and train QC biochemistry analysts Troubleshoot assays like gel electrophoresis and ELISA Ensure cGMP compliance and documentation standards Oversee lab...

As QA Drug Substance Operations Specialist, you will be responsible for providing online QA oversight to Drug Substance manufacturing operations in WuXi Biologics in Dundalk, Ireland. This is a crucial role within the Quality organisation with responsibility for directly supporting the manufacturing operations team daily, ensuring compliance with cGMP and...

LotusWorks is an Engineering Services provider specializing in managing Commissioning, Construction Services, Calibration, Operations & Maintenance scopes of work within global manufacturing facilities. LotusWorks operates globally across EMEA and North America partnering with the world’s leading manufacturers across the Semiconductor, Pharmaceutical...

Overview BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting‑edge manufacturing processes and sites, provide quality assurance and...

Join a leading biologics service provider in Dundalk, Ireland as a QA Drug Substance Operations Specialist. In this pivotal role, you will oversee QA compliance during manufacturing operations, ensuring adherence to cGMP standards. Candidates with a Bachelor’s degree in a technical field and experience in the biotechnology or pharmaceutical industry are...

Clinical Data Management Lead page is loaded## Clinical Data Management Leadlocations: Reading, Berkshire, United Kingdom: Zaventem, Belgium: Dublin, Irelandtime type: Full timeposted on: Posted Todayjob requisition id: R1519074**IQVIA is growing Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and...