Quality Document Specialist

Quality Document Author RoleCK Group is seeking a skilled Quality Document Author to contribute to the success of a global pharmaceutical company.Key ResponsibilitiesDevelop and author qualification documents for Quality control department equipment, ensuring compliance with regulatory requirements.Write and maintain protocols for qualification documents and...

Job Role:Quality Assurance Specialist (CSV Computer Systems Validation)Job Summary:Radiant Systems Inc is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our computer systems and equipment.Key Responsibilities:Author of qualification documents:...

Job Role:Quality Assurance Specialist (CSV Computer Systems Validation)Job Summary:Radiant Systems Inc is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our computer systems and equipment.Key Responsibilities:Author of qualification documents:...

Job Title: Quality Assurance SpecialistAbout the Role:As a Quality Assurance Specialist at Radiant Systems Inc, you will play a crucial role in ensuring the quality of our equipment and systems. Your primary responsibility will be to author qualification documents for the Quality Control department's equipment, including CSV, VP, FDS, and URS. You will also...

Job Title: Quality Assurance SpecialistAbout the Role:As a Quality Assurance Specialist at Radiant Systems Inc, you will play a crucial role in ensuring the quality of our equipment and systems. Your primary responsibility will be to author qualification documents for the Quality Control department's equipment, including CSV, VP, FDS, and URS. You will also...

Job Title: Quality Assurance SpecialistAbout the Role:As a Quality Assurance Specialist at Radiant Systems Inc, you will be responsible for ensuring the quality of our equipment and systems. This involves authoring qualification documents, writing protocols, and coordinating with various teams to execute qualifications.Key Responsibilities:Develop...

Job Title: Quality Assurance SpecialistAbout the Role:As a Quality Assurance Specialist at Radiant Systems Inc, you will be responsible for ensuring the quality of our equipment and systems. This involves authoring qualification documents, writing protocols, and coordinating with various teams to execute qualifications.Key Responsibilities:Develop...

**Job Summary**Radiant Systems Inc is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our computer systems and equipment.Key Responsibilities:Author of qualification documents for Quality control department equipment's, including CSV, VP, FDS, URS,...

Job DescriptionRole: Quality Assurance SpecialistJob Summary:Radiant Systems Inc is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our products and services.Key Responsibilities:Author of qualification documents: Develop and maintain qualification...

Position OverviewQuality Assurance SpecialistRuncornAttractive Salary with Performance IncentivesAre you a seasoned Quality Assurance expert eager to elevate your career within the pharmaceutical sector? Our thriving, multi-location pharmaceutical organization is in search of a qualified Quality Assurance Specialist to become a vital part of our team on a...

About the RoleWe are seeking a highly skilled Quality Control Administrator to join our team at Teva, a global pharmaceutical company. As a Quality Control Administrator, you will play a critical role in ensuring the quality and integrity of our products.Key ResponsibilitiesEnsure compliance with company policies, procedures, and standards, including cGMP,...

About the RoleWe are seeking a highly skilled Quality Control Administrator to join our team at Teva, a global pharmaceutical company. As a Quality Control Administrator, you will play a critical role in ensuring the quality and integrity of our products.Key ResponsibilitiesEnsure compliance with company policies, procedures, and standards, including cGMP,...

{"h1": "Document Controller/Administrator Opportunity", "p": "A dynamic and exciting opportunity has arisen for a Document Controller/Administrator to join a leading business in their sector. This role offers a unique blend of administrative and technical skills, with a focus on managing project information and ensuring an up-to-date and traceable archive.",...

{"h1": "Document Controller/Administrator Opportunity", "p": "A dynamic and exciting opportunity has arisen for a Document Controller/Administrator to join a leading business in their sector. This role offers a unique blend of administrative and technical skills, with a focus on managing project information and ensuring an up-to-date and traceable archive.",...

Job Role:Author of qualification documents for Quality control department equipment's.Key Responsibilities:Writing the protocols required for qualification documentsCoordinating with CSV, QA and IT team and external vendor for execution of the qualificationsWriting user SOP's for the equipment's with in the Quality Control departmentAbout the Company:i-Pharm...

Job Role: Quality Assurance SpecialistLocation: Remote (with option of onsite working, to be discussed)Duration: 12 MonthsAbout the Role:The following information aims to provide potential candidates with a better understanding of the requirements for this role.Job Responsibilities:Author of qualification documents for Quality control department equipment's...

Job Role: Quality Assurance SpecialistLocation: Remote (with option of onsite working, to be discussed)Duration: 12 MonthsAbout the Role:The following information aims to provide potential candidates with a better understanding of the requirements for this role.Job Responsibilities:Author of qualification documents for Quality control department equipment's...

Role: Quality Assurance Specialist (CSV Computer Systems Validation)Location: Runcorn, UK.Duration: 12 MonthsThe following information aims to provide potential candidates with a better understanding of the requirements for this role.Description:Onsite (with option of remote working, to be discussed)Job role is:1. Author of qualification documents for...

Role: Quality Assurance Specialist (CSV Computer Systems Validation)Location: Runcorn, UK.Duration: 12 MonthsThe following information aims to provide potential candidates with a better understanding of the requirements for this role.Description:Onsite (with option of remote working, to be discussed)Job role is:1. Author of qualification documents for...

Award-Winning Business Seeks Document Controller/AdministratorA dynamic opportunity has arisen for a skilled Document Controller/Administrator to join a global leader in their sector. This role offers a unique blend of administrative and technical responsibilities, making it an ideal fit for a detail-oriented and organized individual.Key...