validation lead

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...

. 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...

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...

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...

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...

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...

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...

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,...

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...

Amgen in Dun Laoghaire, Ireland, is seeking a Sr. Validation Engineer to support day-to-day operation of automation systems at its aseptic drug product facility.You will focus on maintaining validated state, compliance documentation, and cross-functional collaboration to ensure continuous improvement. Ideal candidates have 5+ years in compliance or...

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...

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...

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...

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...

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...

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...

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...

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...

Regeneron is seeking a Senior QA Validation Specialist to join their Quality Assurance team in Limerick. Please ensure you read the below overview and requirements for this employment opportunity completely. This role involves generating, executing, and reviewing validation protocols while ensuring compliance with industry regulations. Candidates should...