Sr. Validation Specialist - Stamullen, County Meath

We are PCI. · Bridge to thousands of biopharma companies and their patients. · ...

We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. · ...

The role of the Senior Validation Specialist is to implement and execute tasks relating to operational support for product launches, · Process, Facility and Equipment Development at PCI Pharma Services sites. · Support the validation effort for all Strategic Projects on site. · ...

+Job summary · Life changing therapies. Global impact.Bridge to thousands of biopharma companies and their patients. · We are PCI. · Main purpose of the jobThe role of the Senior Validation Specialist is to implement and execute tasks relating to operational support for product l ...

We are looking for a Validation Specialist (Permanent role) to join our team in Stamullen, · County Meath. This is a Monday to Friday position. · Ensure safe work practices are being followed at all times. · To implement and execute tasks relating to Process, Facility and Equipme ...

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. · Bachelor's or associate degree or Diploma / Certificate in Quality / Validation. · 2-5 years' experience working in Validation. · ...

We are PCI. · Our investment is in People who make an impact, · drive progress and create a better tomorrow. We · are looking for a Validation Specialist, to join our team in Stamullen, · County Meath. This is a Monday to Friday position, · 100% on-site. ...

We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. · Implement and execute tasks relating to Process, Facility and Equipment Development at PCI Pharma Services sites. · Ensure safe work practices are being followed at all time ...

This role is responsible for overseeing all validation activities ensuring compliance with current regulatory requirements cGMP and company SOPs It includes validation/qualification activities for facilities utilities equipment computerised systems cleaning processes storage area ...

Our client is seeking a Manufacturing/Validation Specialist to join their team in Arnhem. · The successful candidate will have experience working in a pharmaceutical laboratory environment and knowledge of laboratory instrument systems. · ...

PSC Biotech is a leading manufacturer of biopharmaceuticals. · The Senior Validation Specialist will be responsible for ensuring the quality oversight of qualification/validation activities and maintaining an understanding of cGMP regulations and guidance in relation to all aspec ...

The QA CSQ/CQV specialist will be reporting to the QA CSQ/CQV Lead. This role is responsible for oversight of all validation activities ensuring compliance with current regulatory requirements, cGMP and company SOPs. · ...

This role is responsible for overseeing all validation activities to ensure compliance with current regulatory requirements and company SOPs. It includes validation/qualification activities for facilities, utilities, equipment, computerised systems etc. · ...

The role: QA Validation Specialist on behalf of a leading pharmaceutical company based in Dundalk. · ...

Implement and execute tasks relating to operational support for product launches at PCI Pharma Services sites. · ...

PSC Biotech está buscando a un Especialista Senior en Validación para su calidad. Será responsable de la supervisión de las actividades de validación asegurando el cumplimiento con los requisitos regulatorios actuales, cGMP y SOPs del compañía. · ...

We are PCI. · Our investment is in People who make an impact, · drive progress and create a better tomorrow.Equal Employment Opportunity (EEO) Statement · ...

The QA Systems & Validation Specialist is responsible for ensuring that all GMP-related changes, systems and validation activities comply with regulatory requirements and site Quality standards. · ...

The Computerized System Validation Specialist will work with Customer Validation Unit, IT and cross functional departments in development and implementation of an efficient Computerized Systems Validation Program for automated equipment, processes, and information management syst ...

The QA Systems & Validation · Specialist is responsible for ensuring that all GMP-related changes, · systems, and validation activities comply with · regulatory requirements and site Quality standards.This role provides subject matter expertise across · change control, validatio ...