We are looking for a detail-oriented QMS Auditor to support the implementation, monitoring, and continuous improvement of the Quality Management System (QMS) across the institution. The candidate will assist in internal audits, documentation, compliance monitoring, and corrective action follow-ups in accordance with ISO 9001:2015 standards.
ROLES AND RESPONSIBILITIES
Conduct internal audits across departments to verify compliance with established policies, procedures, SOPs, and quality standards.
Monitor adherence to ISO 9001:2015 requirements and the institution’s Quality Management System.
Review departmental documents, records, process manuals, checklists, and audit evidence.
Identify non-conformities, process gaps, and areas for improvement during audits.
Prepare audit reports and maintain records of audit findings and observations.
Coordinate with department heads and process owners to implement corrective and preventive actions.
Follow up on corrective actions and verify their effective closure within the specified timelines.
Maintain QMS documentation, including audit schedules, checklists, reports, and compliance records.
Assist in preparing for external audits, ISO certification, and surveillance audits.
Support the standardization and improvement of institutional processes and documentation.
Conduct awareness sessions for employees on quality procedures and compliance requirements, as assigned.
... appropriate records and documentation for audit readiness. 2. Internal Audits – QEHS & 5S - Coordinate and support the internal audit schedule. - Assist internal auditors and auditees in planning and executing audits. - Follow up on audit findings and ensure proper documentation of observations and non-conformities. - Track ...
... audit, DHF / DMR / DHR, risk management, process validation (IQ/OQ/PQ), complaint handling, EU IVDR awareness. Preferred / Good to Have - ISO 13485 Internal Auditor / Lead Auditor certification - CDSCO licensing exposure (MD-05/MD-09) and eQMS software experience. - IVD-reagent (not only device) QA background. What We Offer ...
Job Description : Deputy Manager – Production QMS (OSD) Experience: 8–12 Years Department: Production – OSD Key Responsibilities - Ensure implementation and compliance with cGMP, SOPs, and regulatory requirements in OSD manufacturing. - Manage Production QMS activities, including deviations, investigations, CAPA, change ...
... and stakeholder management skills.- Ability to work effectively across cross-functional https://jobeax.com/link/kl7fzftAPuPyCZOO : - ISO 27001 : 2022 Internal Auditor or Lead Auditor Certification (any one mandatory).- ITIL Foundation Certification.- Lean Six Sigma Green Belt or equivalent quality https://jobeax.com/link/60UEyC9IHKduB0eA ...
... Pokyoke, Traceability, Traveller card adherence, Data management system Compliance & Quality Systems - Ensure compliance with IATF 16949, ISO 9001, VDA, IMS, QMS or applicable quality standards. - Support internal, customer, and certification audits. - Maintain audit records and documentation. Data Analysis & Reporting ...
... Support other activities related to distribution management, third-party supplier management, and ESG processes as needed To ensure requirements of the following GS QMS procedures are implemented and maintained: - SSU-SOP-1904 Distributor Management - SSU-SOP-01206 Supplier Audits - SSU-SOP-01204 Supplier Controls - SSU-SOP-0210 ...
... or Electrical Engineering. - Experience: 10 to 12 years of experience in the Wind Renewable Energy, Solar, and T&D sectors. - Certifications: Certified Lead Auditor QMS-9001/45001/14001 is desirable. - Languages: English, Hindi, and Kannada, with proficiency in Hindi and English. - Key Result Areas (KRAs): Theoretical and ...
... configurations. - Direct data migration and integration initiatives, ensuring seamless connectivity between Veeva Vault and enterprise systems such as Clinical, QMS and other Document Management platforms. - Establish and maintain comprehensive system documentation, including design specifications, configuration guides, validation ...
... procedure and Radiography is desirable. An AS9100 Lead Auditor qualification is useful but not mandatory . Demonstrated experience building and implementing a QMS is more important. What Success Looks Like First 30 days · Complete the AS9100 gap assessment. · Establish the QMS architecture and document-control framework. ...