Quality Management System QMS Assistant Manager with 5 to 7 yrs 2026 (Chennai)

Quality Management System QMS Assistant Manager with 5 to 7 yrs 2026 (Chennai)

06 Aug
|
Green Success Infotech
|
Chennai

06 Aug

Green Success Infotech

Chennai

Quality Management System /(QMS/) Assistant Manager with 5 to 7 yrs 2026 Your main goal is to maintain corporate compliance, minimize systemic risks, and ensure that the company s Standard Operating Procedures /(SOPs/) accurately reflect daily operations while meeting rigid international standards.

Key Responsibilities 1.

Audit

Management & Ownership Lead Internal Audits/: Design, schedule, and execute the annual internal audit program across all departments /(Operations, HR, Procurement, Engineering/).

Host External Audits/: Act as the primary liaison or co/-host for Registrar/Notified Body audits, customer corporate audits, and regulatory inspections.

NC Tracking/: Manage the lifecycle of Non/-Conformances /(NCs/) found during audits, ensuring departmental owners complete root/-cause analyses timely. 2.

Document Control

System /(DCS/) Governance Architecture/: Oversee the creation, revision, and obsolescence of Tier 1 /(Quality Manual/), Tier 2 /(Procedures/), Tier 3 /(Work Instructions/), and Tier 4 /(Forms/Records/) documentation.

Digitization/: Frequently responsible for managing or implementing Electronic QMS /(eQMS/) software like MasterControl, TrackWise, or ETQ Reliance.





- Systemic CAPA & Continual Improvement Systemic Oversight/: Unlike a product CAPA /(which fixes a broken tool/), you look at process CAPAs. If multiple departments miss calibration deadlines, you fix the calibration tracking system itself.

Management Review/: Aggregate quality data, audit trends, and CAPA metrics to prepare the quarterly or annual Management Review presentation for executive leadership.

- Industry/-Specific Compliance Ownership Depending on the sector of your facility, you are expected to be a Subject Matter Expert /(SME/) in at least one of these frameworks/: Automotive /(IATF 16949/)/: Deep alignment with the AIAG Core Tools /(APQP, PPAP, FMEA, MSA, SPC/) and customer/-specific requirements.

Medical

Devices /(ISO 13485 / FDA 21 CFR Part 820/)/: Ensuring strict compliance with design controls, risk management /(ISO 14971/), validation protocols, and data integrity. Aerospace /(AS9100/) or General /(ISO 9001/)/: Managing configuration control, counterfeit part prevention, and risk/-based thinking.

Exp /: 5 to 8 yrs Location /: chennai, Sriperumbudur Salary /: best in industry Edu /: BE / Btech / Dip Regards, Nedhra /-HR

📌 Quality Management System QMS Assistant Manager with 5 to 7 yrs 2026 (Chennai)
🏢 Green Success Infotech
📍 Chennai

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