Documentation Specialist I

Job Title: Documentation Specialist IJob Summary:We are seeking a skilled Documentation Specialist I to join our team at Gaming Laboratories International. As a Documentation Specialist I, you will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research.Key...

Bilingual Document Specialist I (English/Spanish) We are seeking a Documentation Specialist I to enhance our Quality Assurance team. This role is crucial in ensuring the integrity of documentation within the gaming and gambling sector. Key Responsibilities: The Documentation Specialist I will be tasked with: Reviewing engineering test files to ensure...

Bilingual Document Specialist I (English/Spanish) As a key player in the gaming industry, Gaming Laboratories International (GLI) has been providing exceptional services for over three decades. We are currently seeking a Documentation Specialist I to enhance our Quality Assurance (QA) team. Position Overview: The Documentation Specialist I will play a...

Bilingual Document Specialist I (English/Spanish) We are seeking a dedicated Documentation Specialist I to enhance our Quality Assurance team. Position Overview: The Bilingual Document Specialist I plays a crucial role in ensuring compliance with regulatory standards by meticulously reviewing engineering test files, compiling necessary certification...

Bilingual Document Specialist I (English/Spanish) As a leader in the gaming services sector, Gaming Laboratories International (GLI) has been committed to excellence for over three decades. We are currently seeking a Documentation Specialist I to enhance our Quality Assurance (QA) team. Position Overview: The role of Document Specialist I involves...

Bilingual Document Specialist I (English/Spanish) As a leading entity in the gaming and certification sector, Gaming Laboratories International (GLI) is in search of a Documentation Specialist I to enhance our Quality Assurance (QA) team. Position Overview: The Bilingual Document Specialist I will play a crucial role in ensuring that engineering test...

Bilingual Document Specialist I (English/Spanish) As a leading entity in the gaming and certification sector, Gaming Laboratories International (GLI) has been committed to excellence for over three decades. We are currently seeking a Documentation Specialist I to enhance our Quality Assurance (QA) team. Location: Global About Us: With a rich history of...

The OpportunityTeva Pharmaceuticals is seeking a meticulous Documentation Specialist to ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. In this role, you will work closely with operators and collaborate with various departments, including Parenterals, Quality Assurance, and Packaging.Key...

Job Title: Document Specialist IGaming Laboratories International (GLI) is seeking a highly skilled Document Specialist I to join our QA team in the Netherlands.Job Summary:The Document Specialist I will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research. This role...

Job Title: Document Specialist IJob Summary:Gaming Laboratories International (GLI) is seeking a highly skilled Document Specialist I to join our QA team. As a Document Specialist I, you will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research.Key...

The OpportunityTeva Pharmaceuticals is seeking a meticulous Documentation Reviewer to ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. As a key member of the production department, you will work closely with operators and collaborate with various departments, including Quality Assurance and...

Job Title: Document Specialist IGaming Laboratories International (GLI) is seeking a highly skilled Document Specialist I to join our QA team in the Netherlands.About the Role:The successful candidate will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research. This...

Job Title: Document Specialist IGaming Laboratories International (GLI) is seeking a highly skilled Document Specialist I to join our QA team. As a key member of our team, you will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research.Key Responsibilities:Maintain an...

The OpportunityTeva Pharmaceuticals is seeking a meticulous Documentation Reviewer to ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. This role is essential in maintaining the highest standards of compliance and quality in our production operations.Key ResponsibilitiesProvide real-time...

The OpportunityTeva Pharmaceuticals is seeking a meticulous Documentation Reviewer to ensure the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process. This role is essential in maintaining the highest standards of compliance and quality in our production operations.Key ResponsibilitiesProvide real-time...

Document Reviewer Job DescriptionGaming Laboratories International (GLI) is a leading gaming services company with a global presence. We are seeking a skilled Document Specialist I to join our QA team in the Netherlands.The successful candidate will be responsible for reviewing engineering test files for regulatory compliance, compiling certification...

Job Title: Document Specialist IGaming Laboratories International (GLI) is seeking a highly skilled Document Specialist I to join our QA team in the Netherlands.About the Role:The Document Specialist I will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research. This...

Job Title: Quality Assurance SpecialistAbout the Role:We are seeking a Quality Assurance Specialist to join our team at Teva Pharmaceuticals. As a Quality Assurance Specialist, you will be responsible for ensuring the accuracy, completeness, and compliance of all documentation throughout the drug manufacturing process.Key Responsibilities:- Provide real-time...

The OpportunityAs a Process Control Specialist at Teva Pharmaceuticals, you will play a pivotal role in ensuring the smooth operation of our aseptic manufacturing site. You will lead a team of operators, specialists, and technicians, overseeing production planning, monitoring automated processes, and enforcing quality and safety regulations.Key...

Job Title: Bilingual Document SpecialistJob Summary:Gaming Laboratories International (GLI) is seeking a Bilingual Document Specialist to support our QA team. The successful candidate will be responsible for reviewing engineering test files for regulatory compliance, compiling certification documents, and conducting related research.Key...