Search Results: 27 vacancies
...Ensure audit readiness by complying with effective standards, regulatory / statutory; GEP, GDP and cGMP requirement.
Ensure all work activities... ...Experience in preparing GMP documents (eg. Deviation report, IOQ Protocols, Change Control and SOPs)
To learn more about...
...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 that batch record,...
...meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United... ...qualification activities
Provide support for generating protocols/reports for validation
What are we looking for?
Educational...
...meet the high quality and good manufacturing standards of global regulatory bodies such as the European Medicines Agency and the United... ...movements of people resource
Have a view to analyze CAPMAN
Reporting based on new process flow
What are we looking for?
Educational...
...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 that batch record,...
...lay outs and block diagrams).
Execute and review SAT protocol/report
Execute and review equipment Mechanical Completion and... ...work.
Manage mechanical equipment inspections to meet local regulatory requirement.
Maintain and participate in implementation of EHS...
...ensure that the tests are analyzed in accordance with corporate, regulatory and external agency regulations.
Enforce all laboratory... ...Preferably with knowledge of statistics
Business
Effective report writing skills Planning and Organizing skills
Good interpersonal...
...and Health, Safety and Environment (HSE) regulations and other regulatory standards.
The Senior/ Operations Supervisor is a First Line... ...production site in Belgium RX59 to Singapore (SG) Tuas.
This role reports to the Operations Lead and will support him/her in any other...
...verification of task and data
Assist in SOP writing
Identify and report problems in QC to QC Superintendent in a timely manner... ...to ensure accuracy of test results in accordance with corporate, regulatory and external agency regulations.
Provides training to the team...
...programs by reviewing operations, quality control and maintenance reports and statistics; inspect operating equipment and systems for... ...System) to meet cGMP, GSK guidelines / policies, site procedures and regulatory guidance by ensuring all new engineering CAPEX / Modification is...
...ensure QC operations are in compliance to applicable corporate, regulatory and external agency regulations
Leads/ manages investigation... ...events/ deviations, CAPAs and GMP documents (e.g. SOP, protocols, reports)
Provides technical expertise and consultation to routine...
4700 SGD
...Assist in reviewing contracts, ensuring compliance with legal and regulatory requirements.
• Collaborate with legal and procurement teams to... ...for potential projects.
• Assist in preparing financial reports, forecasts, and budgetary recommendations for management.
5....
Index-cool Design & Furnishing Pte Ltd
Tuas, Singapore Country
8 days ago
...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...
...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...
...Sterility Assurance aspects of site manufacturing processes and products manufactured by the site are compliant with GSK standards and regulatory requirements.
Provide input on aspects relating to Sterility Assurance for qualification and validation strategies.
3....
...Sterility Assurance aspects of site manufacturing processes and products manufactured by the site are compliant with GSK standards and regulatory requirements.
Provide input on aspects relating to Sterility Assurance for qualification and validation strategies
Management...
...Professional
~ At least University basic degree in a Science or Engineering discipline
Technical
A good understanding of cGMP regulatory and legal requirements as applied to quality assurance of pharmaceuticals manufacturing
User experiance with SAP will be prefered...
