Calibration & Maintenance3
Manage the calibration and maintenance schedules for equipment, track maintenance activities, and ensure compliance with calibration requirements.
Revision Control3
Ensure all docs and specs have proper documentation, review, and approval of changes & revisions by the right people.
Training3
Ensure employees are trained on safety practices and quality procedures, including when controlled docs are revised.
Complaint Handling3
Capture, document, and track customer complaints, initiate investigations, implement corrective actions, and analyze complaint trends.
Risk Management3
Identify and mitigate risks during product design and production stages
Electronic Batch Records3
Capture critical batch info such as materials used, manufacturing steps, calibration, QC tests, batch releases.
EH&S3
Track and manage safety incidents, risks, EH&S audits, regulatory compliance, environmental protection, etc.
Security & Access Controls3
Implement robust security measures to protect sensitive data, ensure user access controls, and maintain audit trails for system activities.
Regulatory & Compliance3
Ensure adherence to relevant regulatory requirements, such as ITAR, AS 9100, AS 9110, AS 9120 and other applicable standards.
Change Control3
Controlled management of changes to device design or production process with proper review and approval.
Approval Workflows3
Implement approval workflows within the QMS that allow for electronic signatures.
First Article Inspection3
Validate that product design and production processes produce items meeting specified design requirements.
Performance Metrics and Reporting3
Generate reports, dashboards, and analytics on key quality metrics, performance indicators, and trends to enable data-driven decision-making.
Document Management3
Control, track and manage documents required for compliance with AS 9100, 9110, 9120, ISO 9001
Audit Management3
Plan, schedule, and conduct internal, layered and external audits for compliance verification.
Supplier Quality3
Manage the qualification, evaluation, and monitoring of suppliers, including conducting supplier audits, tracking supplier performance, and maintaining supplier documentation.
Integration & Collaboration3
Integrate with other systems and tools, such as ERP systems, CRM systems, and collaboration platforms to facilitate seamless information exchange and workflow management.
ITAR Compliance3
Ensure all ITAR controlled docs & data are stored in compliant locations and retrieved only by authorised individuals.
FMEA3
Identify and discuss failure modes, causes, effects, severity, detection, risk priorities of your product, design & process
Product & Raw Material Specifications3
Collaborate on drawings, work instructions, material & process specs, test specs, regulatory requirements and other docs
CAPAS & NCs3
Identify, document, and resolve non-conformities; implement corrective/preventive actions.