This role is responsible for executing manufacturing and packaging operations within a regulated pharmaceutical environment, ensuring products are packed accurately, efficiently, and in compliance with cGMP and global regulatory requirements. The role oversees packaging lines including CVC lines,
Description: This role is responsible for supporting packaging operations within pharmaceutical manufacturing environments as a trainee associate, developing foundational competencies in pharmaceutical packaging processes, equipment operation, and quality compliance. The incumbent assists in performing packaging activities including the operation
Job Description Comply with all cGMP, GxP, and any other applicable regulatory requirements, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
Career CategoryRegulatory Job Description Regulatory Labeling Manager will support the planning, coordination, and execution of EU and global labelling compliance activities within the Regulatory Affairs organisation. This role will support end-to-end labelling activities, including Product Information
Job Description Purpose of the Role To operate, maintain, calibrate, troubleshoot, and improve instrumentation and automation systems used in pharmaceutical manufacturing facilities, ensuring uninterrupted operations, regulatory compliance, data integrity, equipment reliability, and adherence to cGMP requirements.
About CapGrid CapGrid is a leading supply chain technology company focused on end-to-end sourcing, procurement, and vendor ecosystem solutions for manufacturing companies. We work across multiple categories and specialize in delivering cost optimization, supply assurance, and
ACG is the world’s only integrated pharma manufacturing solutions company. We are headquartered in Mumbai , India. ACG has a presence in over 100 countries with its products and services that strive to provide world-class technology
Job Description Purpose of the Role To operate, maintain, calibrate, troubleshoot, and improve instrumentation and automation systems used in pharmaceutical manufacturing facilities, ensuring uninterrupted operations, regulatory compliance, data integrity, equipment reliability, and adherence to cGMP requirements.