Search Results: 32 vacancies
...manner, drug substance batch review/release are in full gmp compliance to regulatory standards and ensures quality strategy/continuous improvement... ...; Operational Excellence; Digital & Tech Savvy
• MS Office applications and other standard IT applications supporting Quality...
...biopharmaceutical QC activities to ensure QC operations are in compliance to applicable corporate, regulatory and external agency regulations
Leads/ manages... ...Good command of English
Good knowledge of Microsoft office
Attributes required of the job e.g. the ability to...
...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 to...
...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 function
Ensure...
...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 function
Ensure...
...meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United... ...and promote improvements to the site’s safety culture
Conduct office and site inspections, support problem solving, root cause analyses...
...meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United... ...Ensure that the project execution activities are carried in a compliance manner to company policies and regulatory guidelines.
Implement...
...Purpose
Responsible for sterility assurance programme and ensure compliance with company polices and current GMP expectations.... ...manufactured by the site are compliant with GSK standards and regulatory requirements.
Provide input on aspects relating to Sterility...
...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.
Responsibilities...
...ensures that the tests are analyzed in accordance with corporate, regulatory and external agency regulations.
Ensures that all in-use... ...-ordinates with relevant parties. Reviews QC reports to ensure compliance and promptness of results.
Problem solving
Identifies and...
...primarily responsible for the sterility assurance program and ensure compliance with company polices and current GMP expectations.
Key... ...manufactured by the site are compliant with GSK standards and regulatory requirements.
Provide input on aspects relating to Sterility...
...oversight of Supplier management activities on site to achieve compliance with company policies and government regulations as assigned.... ...Engineering discipline
Technical
A good understanding of cGMP regulatory and legal requirements as applied to quality assurance of...
...administrator of the Site Document Management System and perform required compliance related checks for documents.
Issue controlled documents (e.g... ...GMP experience preferred
Computer skills in MS Office (Microsoft Word, using and presenting database software such as...
...the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing...
...the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing...
...documentation and record system to ensure quality assurance operations.
Ensure audit readiness by complying with effective standards, regulatory / statutory; GEP, GDP and cGMP requirement.
Ensure all work activities are carried out according to site procedures and standards...
...the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing...
...the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing...
...the facility became operational in 2011. The facility and operations meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United States Food and Drug Administration.
Tuas is a key manufacturing...
...Singapore, and GSK and site EHS / Engineering standards and procedures at work.
Manage mechanical equipment inspections to meet local regulatory requirement.
Maintain and participate in implementation of EHS programmes.
Maintain relevant EHS qualifications and...
