- Location
- Bangalore - HO, India
- Type
- Full-time
- Seniority
- Manager
- Experience
- 25+ years
- Source
- Workday
Description
ZEISS in India
ZEISS in India is headquartered in Bengaluru and present in the fields of Industrial Quality Solutions, Research Microscopy Solutions, Medical Technology, Vision Care and Sports & Cine Optics.
ZEISS India has 3 production facilities, R&D center, Global IT services and about 40 Sales & Service offices in almost all Tier I and Tier II cities in India. With 2200+ employees and continued investments over 25 years in India, ZEISS’ success story in India is continuing at a rapid pace.
Further information at ZEISS India.
Position summary:
The QMS Manager – Quality & Digital Systems plays a key role in shaping, maintaining, and continuously enhancing the global Quality Management System (QMS) for medical devices across ZEISS Vision Care.
This role ensures end-to-end compliance with applicable international standards and regulatory requirements (e.g., ISO 9001, ISO 13485, MDSAP, MDR and relevant GxP expectations).
Primary duties and responsibilities.
QMS maintenance and improvement:
- Own and support the lifecycle management and continuous improvement of the QMS in alignment with global regulatory standards
- Identify systemic process gaps and drive structured risk-based assessments
- Lead and support implementation of effective corrective and preventive actions (CAPA) to ensure long-term compliance and process stability
Audit program support:
- Lead planning, coordination, and execution of internal and external audits using a risk-based audit strategy
- Ensure structured preparation, documentation, and timely closure of audit findings
- Strengthen overall audit readiness across regions, ensuring consistent compliance performance
Management reporting:
- Lead preparation and analysis of QMS performance metrics for management review
- Support structured execution of Management Review Meetings, including tracking of resulting actions
- Manage and govern Change Review Board (CRB) processes, ensuring effective evaluation and controlled implementation of quality-relevant changes
Digital quality systems:
- Drive design, implementation, validation, and lifecycle management of digital quality systems (eQMS, RIMS, and related platforms)
- Ensure full compliance with Computer System Validation (CSV) principles and data integrity requirements
- Enable digital transformation of QMS processes through harmonized system architecture and governance
Continuous improvement:
- Analyze quality data, audit outcomes, deviations, and KPIs to identify improvement opportunities
- Lead and support cross-functional improvement initiatives across NC/CAPA, document control, complaints, and deviation management
- Promote a culture of quality excellence and sustainable process improvement
Training and support:
- Design and support QMS-related training programs across systems and processes
- Provide expert guidance to stakeholders on regulatory and QMS requirements
- Strengthening organizational capability through coaching and best practice sharing
External interfaces:
- Support engagement with notified bodies, certification bodies, and external auditors
- Ensure structured preparation and execution of external inspections and audits
Education / Professional Certification:
- Bachelor’s or Master’s degree in engineering, natural sciences, or related field
- Strong knowledge of ISO 13485, ISO 9001, MDSAP, and GxP requirements
- Lead Auditor certification is a plus
Experience:
- 3–7 years of experience in Quality Management within regulated industries (medical devices, pharma, or equivalent)
- Proven experience in QMS operations, audits, and compliance management
- 3–5 years of exposure to digital quality systems (eQMS platforms)
- 3–5 years of experience in Computer System Validation (CSV) is a strong advantage
Knowledge / Skills / Other characteristics:
- Strong understanding of QMS frameworks and regulatory requirements
- Solid knowledge of audit methodologies and CAPA lifecycle management
- Hands-on experience with eQMS platforms (e.g., TrackWise, Veeva, Dot Compliance)
- Strong analytical, problem-solving, and data interpretation skills
- Excellent stakeholder management and communication skills
- Ability to operate effectively in global, cross-functional environments
- Fluent English required; German is an advantage
Your ZEISS Recruiting Team:
Itishree Pani