Conference Room Prep: Ensuring meeting rooms are properly set up, and basic fixtures like whiteboard mounts or projector, TVs, AV system, Audio system and HDMI connection are secure.
Managing the operable wall for 3 collapsible meeting rooms.
Enforce security procedures in accordance with government regulations, corporate policies, and standard operating procedures.
Conduct scheduled visits to CelcomDigi premises and sites nationwide to audit, review, and assess physical security performance, including identifying opportunities for system enhancements.
Implement and support the design of security technology and digital initiatives, including developing, integrating, documenting, and enforcing standards and procedures, as well as assessing internal and partner-related risk exposures.
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Responsible for completeness of documentation prior to release of finished products under New Product Development (NPD), cost / quality compliance project with complete Authorization for Product Release (APR) / Global Change Control (GCC) and meeting quality requirement.
Ensure Validation activities such as Equipment & Facilities Qualification, Process Validation, Computer System Validation, etc. of the site are planned and carried out in accordance to Validation Master Plan and Kenvue requirement
Performs review, trending, tracking and monitoring of cGMP processes, procedures, training, documents and records, including but not limited to non-conformance records, change control, and corrective actions / preventive actions (CAPA), complaints investigation through respective electronic platform systems
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Responsible for completeness of documentation prior to release of finished products under New Product Development (NPD), cost / quality compliance project with complete Authorization for Product Release (APR) / Global Change Control (GCC) and meeting quality requirement.
Ensure Validation activities such as Equipment & Facilities Qualification, Process Validation, Computer System Validation, etc. of the site are planned and carried out in accordance to Validation Master Plan and Kenvue requirement
Performs review, trending, tracking and monitoring of cGMP processes, procedures, training, documents and records, including but not limited to non-conformance records, change control, and corrective actions / preventive actions (CAPA), complaints investigation through respective electronic platform systems
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