validation lead

. 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 pioneering new healthcare solutions for...

LSC have a great contract opportunity for a Validation Lead to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could...

The Validation Lead oversees all validation activities related to equipment, utilities, processes, and computerized systems to ensure compliance with regulatory requirements (such as FDA, EMA, and cGMP standards). This role is responsible for planning, coordinating, and executing validation projects, managing documentation, and ensuring validated status is...

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 pioneering new healthcare solutions for diseases with high unmet...

PE Global is recruiting for a Validation Lead for a leading multinational biotech client based in Dublin. This is an initial 12-month contract, fully onsite role. Overview: - Validation lead for a large-scale Fill Finish Project in the Pharmaceutical Industry. Lead a team of Validation engineers to ensure the Validation activities associated with a large...

Overview Due to large scale Biotech project wins we now wish to recruit a Senior CSV Engineer(s) to join a highly skilled PM Group team based a client site. Responsibilities The following is an example of the day to day activities (however like all large capex projects there will be a good deal of variety). Commissioning and Qualification of hardware and...

About AstellasAstellas 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 pioneering new healthcare solutions for diseases with...

Validation lead for a large-scale Fill Finish Project in the Pharmaceutical Industry. Lead a team of Validation engineers to ensure the Validation activities associated with a large fill finish project are completed safely, as per schedule and in compliance with GMP and Quality Requirements.Key Responsibilities:Coordinates and Supervises all Validation...

Astellas is seeking a leader to guide the daily operations of the Validation function at our Tralee site in Ireland. You will manage Validation Engineers (staff and outsourced providers), drive efficiency, and ensure processes, systems, and equipment perform to the highest standards in a GMP environment.Responsibilities include leading the Validation team,...

Life Science Consultants is sourcing a Validation Lead for a South Dublin based biopharmaceutical company. The role requires 7+ years in Validation, Engineering, Microbiology or Quality and hands-on experience with sterile/biotech equipment.The successful candidate will coordinate validation activities and approve planning documents, ensuring quality and...

Regeneron Pharmaceuticals, Inc is seeking a Senior QA Validation Specialist to join their Quality Assurance team in Munster, Ireland. This role involves managing and executing validation protocols, ensuring compliance with regulations, and troubleshooting issues in a dynamic environment.The ideal candidate will have a BS/BA in Engineering, Chemistry or Life...

Regeneron is seeking a Senior QA Validation Specialist to join their Quality Assurance team in Limerick. This role involves generating, executing, and reviewing validation protocols while ensuring compliance with industry regulations. Candidates should possess a BS/BA in Engineering, Chemistry, or Life Sciences and have substantial experience (5–8+ years)...

Morgan McKinley is seeking a QC Chemistry Analyst to support NPI activities and routine QC tasks within the Dublin site. The role requires contributing to method validation, data management, and process improvements, with a focus on analytical testing and regulatory compliance.Under minimal supervision, you will manage samples, coordinate with...

EFOR is seeking a Validation Lead to oversee validation activities across equipment, processes, utilities, and computerized systems in a regulated pharmaceutical environment. You will guide validation projects, maintain documentation, and ensure ongoing compliance with FDA/EMA and cGMP standards.The role requires strong project management, leadership, and...

Regeneron Pharmaceuticals, Inc is seeking a Senior QA Validation Specialist to join their Quality Assurance team in Munster, Ireland. Below covers everything you need to know about what this opportunity entails, as well as what is expected from applicants. This role involves managing and executing validation protocols, ensuring compliance with regulations,...

Fruition Group is seeking an experienced Senior Manager Operational Risk to lead the 2LoD validation for BCBS 239 / RDARR, providing independent oversight and assurance over delivery. You will coordinate validation across data governance, data quality, lineage, controls, and risk reporting, and engage with senior governance forums and regulatory reviews.The...

Regeneron Ireland in Raheen, Limerick is seeking a Senior QA Validation Specialist to join our Quality Assurance team. You will lead end-to-end qualification activities and support a 365 inspection readiness program.The role requires 5–8+ years in pharma/biotech, strong change controls, data integrity awareness, and knowledge of EU Annex 11 and FDA 21 CFR...

A leading company in the life sciences sector is seeking a CQV Engineer to join its growing operations in Ireland. The ideal candidate will oversee Commissioning, Qualification, and Validation activities while managing project documentation and ensuring safety compliance. Candidates should hold a relevant degree and have significant experience in life...

Summary of the Role The Validation Lead is responsible for leading the validation team in the delivery of GMP validation, commissioning and compliance projects across the pharmaceutical, medical device and healthcare sectors. The role combines technical leadership with people management, ensuring projects are delivered safely, on time, within budget and to...

Chanelle Pharma is seeking an experienced Method Development & Validation Analyst to own SIM development, validation, and nitrosamine impurity testing. You will ensure methods meet ICH Q2(R2) and regulatory expectations in a hands‑on analytical chemistry role. You will lead method development, validation, transfer and documentation, while maintaining data...