Compliance specialist jobs in Tuas, Singapore Country

 ...to enable the timely production of products with quality and quantity in compliance with the relevant GMP, safety and environmental guidelines. About the Role Position Title: Equipment Specialist I Location – Singapore About the Role: Execute assigned Manufacturing... 

 ...research support, and stability testing About the Role Position Title : QC Specialist I - Raw Materials Key responsibilities • Maintain QC Raw Materials laboratory in full cGMP compliance. • Lead raw material method validation/ verification and routine release... 

 ...timely manner, drug substance batch review/release are in full gmp compliance to regulatory standards and ensures quality strategy/continuous...  ...to site objective/s. About the Role Position Title : Specialist - QA Ops - Manufacturing Mgmt Location – Singapore About... 

 ...exceptions) and close the report on time. Performs data trending and co-ordinates with relevant parties. Reviews QC reports to ensure compliance and promptness of results. Problem solving Identifies and reports problems in QC. Solve problems and implement corrective... 

 ...biopharmaceutical QC activities to ensure QC operations are in compliance to applicable corporate, regulatory and external agency regulations...  ...and Management Responsibilities Works with senior specialists/ chemists and manager to create a culture of accountability, ownership... 

 ...escort vendor during service and approve invoice timely Supports compliance activities: Performs regular Ll audits in QC Coordinates...  ...training and development Skills: Professional For Specialist - University Degree in a relevant Science discipline with at... 

Site Name: Singapore - Tuas Posted Date: Apr 9 2024 The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation...

 ...proper maintenance of QC IPC/DS (In Process control/Drug Substance) lab equipment and systems and troubleshoot to ensure full cGMP-compliance for shift team. About the Role Position Title: QC Analyst II Location – Singapore About the Role: This role will ensure... 

 ...Associates or Senior, you will be responsible for conducting sample testing of incoming materials and/or finished products to ensure compliance with regulatory agencies’ requirements and company standards. This role will provide YOU the opportunity to lead key activities... 

 ...Maintenance/Equipment, QC) and implementation of Corrective and Preventive Action (CAPA) Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements Reporting/Documentation Operate key computer applications related to... 

 ...ensure documents are ready for approval timely. Be the administrator of the Site Document Management System and perform required compliance related checks for documents. Issue controlled documents (e.g. Batch records, logbooks and sampling labels) in a timely manner, as... 

 .../Equipmen , t QC) and implementation of Corrective and Preventive Action (CAPA) Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements Reporting/Documentation: Operate key computer applications related to production... 

 ...housekeeping is maintained. Maintain awareness in SEHS within maintenance section. Provide full support and accountability on compliance to SSOW system (eg. PTW, LOTO) 4. Quality Ensure that all maintenance and repair/replacement activities are carried out in compliance... 

 ...Manufacturing and Laboratory operations Support qualification activities Ensure that the project execution activities are carried in a compliance manner to company policies and regulatory guidelines. Implement improvements and streamline work processes What are we... 

 ...indicators (KPI) for the supply chain, especially for planning/provisioning monitoring Ensure that routine audits are carried out in compliance with cGMP & authorized procedures and policies Ensure timely maintenance of business master data (planning related) in a... 

 ...Site Name: Singapore - Tuas Posted Date: Apr 24 2024 Purpose Responsible for sterility assurance programme and ensure compliance with company polices and current GMP expectations. Responsibilities 1. QA Oversight Implement sterility assurance programme on... 

 ...Tuas. The Senior QA Validation ensures that all commissioning and qualification activities under the project scope is designed in compliance with all applicable GSK Quality policies, regulatory requirement, and GMP practices/ procedures in place and in use within GSK Tuas.... 

 ...operations. Key Responsibilities: Supplier Management Provide QA oversight of Supplier management activities on site to achieve compliance with company policies and government regulations as assigned. To participate (Executive 1) and to represent the site (Executive 2... 

 ...trainees upon completion of the programme. Purpose: To be primarily responsible for the sterility assurance program and ensure compliance with company polices and current GMP expectations. Key Responsibilities: QA Oversight Implement sterility assurance...