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Manager - Central Quality Assurance (Vendor Management & Compliance), ACG Capsules

icon building Company : Acg
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Job Description - Manager - Central Quality Assurance (Vendor Management & Compliance), ACG Capsules


Position Title: Manager - Central Quality Assurance (Vendor Management & Compliance), ACG Capsules


Organization Context































 



Position Title:



Manager - Central Quality Assurance (Vendor Management & Compliance), ACG Capsules



Employee Name:



 



Grade:



M05 or M06



Department:



Quality and Regulatory Affairs



Location:



Kandivali



Reports to:



Head - Central Quality Assurance, ACG Capsules



Reported by:



2 – Sr. Executives










 


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 a Manager – Vendor Management & Compliance, Central Quality Assurance, Quality and Regulatory Affairs.




  1. Job Objective










  • To lead and govern vendor management and compliance processes across ACG Capsules, ensuring a robust and compliant vendor base.

  •  Drive Quality Management Systems (QMS) while strengthening audit readiness, regulatory compliance, and continuous improvement across sites.




  1. Primary responsibilities









Strategy & Planning


 



  • Define and drive vendor management strategy to ensure availability of qualified and compliant vendors

  • Establish governance framework for vendor qualification, performance monitoring, and requalification

  • Drive standardisation of vendor management across sites

  • Lead audit readiness strategy for internal, external, and regulatory audits

  • Identify risks in vendor quality and compliance systems and implement mitigation plans

  • Drive digitalisation and process improvement initiatives in vendor management and DMS


 


Functional



  • Oversee vendor qualification, evaluation, and approval processes in alignment with regulatory and internal standards

  • Review and approve vendor specifications in alignment with ACG quality requirements

  • Ensure effective management of vendor documentation and compliance through systems/portals

  • Review and approve SOPs related to vendor management and QMS

  • Ensure readiness and compliance of raw material and packaging material specifications

  • Oversee planning and execution of vendor audits and internal audits across sites


Core



  • Own end-to-end vendor compliance and QMS performance across ACG Capsules

  • Drive cross-functional alignment with Procurement, Regulatory, Operations, and Quality teams

  • Lead root cause analysis for critical deviations, audit observations, and vendor-related issues

  • Drive implementation of preventive and corrective actions for vendor complaints to strengthen quality systems

  • Establish performance metrics for vendor quality and audit outcomes

  • Act as escalation point for critical vendor and compliance-related issues

  • Own and monitor regulatory and certification compliance across applicable India and overseas locations, including FDA activities, ISO, EXCiPACT, FSSAI, FDS and other relevant requirements.

  • Ensure timely renewal and maintenance of manufacturing licences, regulatory approvals and applicable quality certifications to support uninterrupted compliant operations.


People Development



  • Lead and develop the vendor management and QMS team

  • Drive capability building on GxP practices, audit readiness, and regulatory compliance

  • Build a culture of quality, compliance, and continuous improvement across teams


 Regulatory & Certification Compliance



  • Ensure compliance with applicable FDA, FSSAI, FDS and other regulatory requirements across India and overseas locations.

  • Ensure timely completion of FDA activities, regulatory audits and inspections wherever required.

  • Ensure valid manufacturing licences, regulatory approvals and certifications are maintained.

  • Oversee applicable ISO, EXCiPACT and other quality certifications for India and overseas locations.

  • Ensure timely closure of regulatory and certification-related observations and CAPAs.


****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.




  1. Key Result Areas










  • Vendor compliance and approval cycle time

  • Audit effectiveness (internal, vendor, regulatory) and closure timelines

  • Change Control, Deviation, and CAPA closure timelines and effectiveness

  • Quality of investigations and reduction in repeat deviations

  • Timely and accurate completion of customer/regulatory questionnaires

  • Vendor performance and quality metrics




  1. Key Interfaces














Internal Interfaces



External Interfaces




  • Purchase Team

  • Regulatory Team

  • Projects Team

  • Operations

  • Corporate Quality




  • Vendors

  • Auditors



 


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