C GMP Documentation Coordinator

About the Role:Pharmagend Global Medical Services Pte Ltd is a leading provider of quality assurance services. We are seeking a highly organized and detail-oriented GMP Documentation Specialist to join our team. In this role, you will be responsible for supporting the preparation of accurate and compliant documentation, ensuring seamless operations and...

Job OverviewSamsung C&T Corporation is seeking a highly organized and detail-oriented Document Controller to join our team. This role is responsible for managing and maintaining the company's important documents and records, ensuring they are organized, accessible, and compliant with relevant policies and regulations.ResponsibilitiesManage and maintain...

The role will involve working within a multidisciplinary team who carry out system performance test, evaluation and customer qualification Responsibilities Technical support of field service engineers and customers when required Evaluating and establishing vision system performance specifications Manage customer specific projects & documents Provide...

Roles & ResponsibilitiesThe role will involve working within a multidisciplinary team who carry out system performance test, evaluation and customer qualificationResponsibilities· Technical support of field service engineers and customers when required· Evaluating and establishing vision system performance specifications· Manage customer specific projects...

KEY DUTIES AND RESPONSIBILITIES: Support the generation of c GMP documentation including qualification protocols, SOP, and production batch record issuance. Co-ordinate internal review and approval of documentation. Proactively progress documents to achieve schedule adherence and to site policies & compliance with c GMPs. Initiate Production Change control,...

Roles & ResponsibilitiesResponsibilities: Design and develop software for automated computer vision systems. Develop software for GUI, big data management, and multi-threaded programming. Create and refine image processing and computer vision algorithms. Participate in the complete Software Development Life Cycle (SDLC).Requirements: PhD, Master’s, or...

We are looking for a skilled GMP Purchaser to join our team at This Is An IT Support Group. The successful candidate will be responsible for managing purchasing activities, including sourcing and procuring materials, supplies, and equipment necessary for our GMP facilities.Duties and Responsibilities:Manage purchasing activities, including sourcing and...

At CRIS, we bring together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system. As a Logistics Coordinator GMP Compliance at CRIS, you will play a key role in ensuring the compliance of our Good Manufacturing Practice...

Roles & ResponsibilitiesThe role involves working within a multidisciplinary team to carry out software development/support for automated computer vision equipmentResponsibilities· Design and develop software for automated Computer Vision Equipment· Software development for GUI, big data management, real time socket communication· Involve in Software...

About Our TeamThe Consortium for Clinical Research and Innovation, Singapore (CRIS) is a leading player in the clinical research and innovation sector. Our team is passionate about advancing clinical research and innovation for Singapore, and we are seeking like-minded individuals to join us.Job SummaryWe are seeking a skilled Purchasing Management...

Responsibilities Design and develop software for automated Computer Vision Equipment Software development for GUI, big data management, real time socket communication Involve in Software Development Life Cycle Technical Support and Deployment   Requirements PHD / Masters / Degree in engineering discipline. Knowledge in programming skills in Visual Studio...

About the RoleThis is an exciting opportunity to join Samsung C&T Corporation as a Document Controller. As a key member of our team, you will be responsible for managing and maintaining the company's important documents and records.Key ResponsibilitiesEnsure that all documents are properly filed, stored, and maintained in accordance with company policies and...

About the role Join Samsung C&T Corporation as a full-time project site Document Controller . In this role, you will be responsible for managing and maintaining the company's important documents and records, ensuring they are organised, accessible and in compliance with relevant policies and regulations. What you'll be doing Manage and maintain...

Job Summary:At Pharmagend Global Medical Services Pte Ltd, we are committed to delivering high-quality services that meet regulatory standards. We are seeking a qualified Quality Document Coordinator to support our operations team. This role involves coordinating the preparation of accurate and compliant documentation, ensuring efficient and effective...

Job DescriptionThe Document Controller will be responsible for managing and maintaining the company's important documents and records, including:Ensuring that all documents are properly filed, stored, and maintained.Liaising with Construction team members to identify their documentation requirements.Managing the disposal and retention of...

Roles & ResponsibilitiesResponsibilitiesManage credit limits and portfolio elements in AS400. Ensure timely regulatory reporting (e.g., MAS, Head Office). Monitor financial documents and covenants using CPS. Review credit and facility documents for accuracy. Safeguard and check facility/security documents annually. Work with CIB and Operations to close...

Responsibilities Design and develop software for automated Computer VisionEquipment Software development for GUI, bigdata management, real time socket communicationInvolve in Software Development Life CycleTechnical Support and Deployment   Requirements PHD / Masters / Degree in engineeringdiscipline. Knowledge in programming skills inVisual Studio...

Roles & ResponsibilitiesResponsibilities Manage credit limits and portfolio elements in AS400. Ensure timely regulatory reporting (e.g., MAS, Head Office). Monitor financial documents and covenants using CPS. Review credit and facility documents for accuracy. Safeguard and check facility/security documents annually. Work with CIB and Operations to...

The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system.As a Supply Chain Manager GMP at CRIS, you will play a key role in ensuring the...

The Advanced Cell Therapy and Research Institute, Singapore (ACTRIS) was established to meet the increasing clinical demand of using cellular therapeutics to treat various life-threatening diseases. As a Procurement Specialist GMP Facility at ACTRIS, you will be responsible for managing the procurement of GMP materials and inventory.You will partner with...