Assistant - Regulatory Affairs, ACG Capsules

Position Title:

Assistant – Regulatory Affairs, ACG Capsules

Employee Name:

Grade:

M09

Department:

Quality and Regulatory Affairs

Location:

Kandivali

Reports to:

Senior Lead - Regulatory Affairs, ACG Capsules

Reported by:

 None

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 across multiple domains. We offer a complete range of solutions beginning with empty capsules; granulation and tablet coating; capsule filling; tabletting; packaging films; blister packing and carton packing to the end-of-line solutions and track and trace systems.

We have an opportunity in ACG Capsules of an Assistant – Regulatory Affairs, Quality and Regulatory Affairs, Central.

• Provide regulatory support to customers in order to meet current and new regulatory norms


• Life cycle management of existing dossier in various countries to meet customer and regulatory norms

Strategic and planning

Functional

Core: -

• Ensure compliance to all regulatory norms (new & existing)


• Prepare & submit Drug Master files in CTD format for the respective regions on annual & biannual basis along with issuance of LOA


• Handling customer questionnaires / specification on timely manner


• Respond to customer / regulatory queries within pre-defined timelines


• Conduct regulatory checks of shades & artwork


• Obtain / renew regulatory certificates on timely manner


• Product – wise ARTG filing in Australia as per timelines and ensure FTR


• Generate & maintain regulatory back-up data to respond to regulatory/customer queries


• Preparation & maintenance of regulatory documentations for existing and new products


• Provide change notifications to customers as and when required


• Check and release dossier in DMS on timely basis


• Provide regulatory support to Plant QA and International RA teams as and when required


• Verify regulatory acceptance of various ingredients in various countries for existing and new products


• Maintenance and updation of data in internal online systems

Internal process:

• Publication of regulatory updates in order to create awareness among internal stakeholders

People development

• Train CSR team and Plant associates (if required) on regulatory requirements

****Any other additional responsibility could be assigned to the role holder from time to time as a standalone project or regular work. The same would be suitably represented in the Primary responsibilities and agreed between the incumbent, reporting officer and HR.

Internal Interfaces

External Interfaces

• CSR


• Sales (TIC)


• Plant Quality & Operational

• Customer


• Certification Agency


• Regulatory Agency