Fire Point Rocket Technology

We specialize in the design and manufacturing of rocket engine components, with qualification and performance testing conducted at our dedicated off‑site facilities.
Our work supports programs of vital importance to Denmark’s national defense.

Role Mission

The Quality Control Manager ensures that every batch of solid propellant and assembled product meets defined quality, safety, and performance standards – from incoming raw materials to final radiographic inspection.

This role acts as the independent eye of quality within production, ensuring that no material or component is released without full verification and documentation.

The QC Manager leads laboratory and NDT (non-destructive testing) operations, ensures compliance with ISO / defense standards, and builds a culture of precision and accountability across all production areas.

Core Responsibilities

• Quality Governance: Define and maintain quality control standards, sampling plans, and inspection procedures across all process stages.

• Incoming Material Control: Manage testing and approval of all incoming materials in coordination with the laboratory (Chief Chemist).

• In-Process Control: Supervise inspections and measurements during mixing, polymerization, and demolding to ensure process compliance.

• Final Product Control: Oversee non-destructive testing (NDT) – radiography, MRI, and pressure/leak tests – to guarantee product integrity and reliability.

• Defect Analysis: Lead root-cause investigations for non-conformities; collaborate with Process Engineering and Production to implement CAPA (Corrective & Preventive Actions).

• Batch Release: Authorize batch release or hold decisions; ensure traceability and documentation completeness before shipment.

• Documentation & Compliance: Ensure full recording of QC data, test results, and reports; maintain records in line with ISO/AQAP and internal audit requirements.

• Calibration & Equipment Management: Ensure regular calibration and maintenance of QC equipment (radiographic devices, pressure testers, gauges, sensors).

• Audit Readiness: Prepare and support internal, customer, and external audits; represent the QC function during inspections.

• Training & Culture: Train operators and supervisors on defect recognition, inspection criteria, and documentation discipline.

• Safety & HSE: Enforce strict adherence to HSE standards within QC areas — particularly radiography, chemical testing, and pressurized systems.

Functional Scope

• Incoming QC: Raw material verification and supplier quality interface.

• In-Process QC: Sampling, dimensional and visual control, monitoring of process deviations.

• Final QC: Radiography, MRI, leak & pressure testing, documentation of results.

• CAPA & Reporting: Non-conformance management, corrective actions, trend reporting.

• Quality Systems: SOPs, calibration, and audit compliance under ISO/AQAP.

Decision-Making Authority

• Approve or reject materials, batches, and components.

• Stop production or block shipment in case of non-conformity or safety risk.

• Define and approve quality inspection standards and documentation templates.

• Propose CAPEX/OPEX improvements related to testing or measurement equipment.

• Initiate and lead internal quality investigations.

Key Performance Indicators

• Right-First-Time rate (batches passing QC without rework).

• Scrap / Rework rate due to quality deviations.

• Timeliness of batch release (no production delay caused by QC bottlenecks).

• Number of recurring defects (CAPA effectiveness).

• Audit non-conformities (internal & external).

• Calibration compliance rate.

• Zero safety incidents in radiography and testing areas.

Qualifications & Experience

• Education: MSc in Chemistry, Materials Science, Mechanical or Industrial Engineering.

• Experience: 7+ years in Quality Control / Assurance within chemical, polymer, aerospace, or defense manufacturing.

• Proven experience with non-destructive testing (NDT) and quality systems (ISO 9001, AQAP, or AS9100).

• Knowledge of radiographic analysis, pressure testing, and sampling methodologies.

• Experience managing CAPA systems and leading internal audits.

• Familiarity with MES / ERP systems for traceability and digital QC data collection.

• Understanding of HSE and radiation safety requirements.

Professional Skills

• Deep understanding of QA/QC principles and documentation flow.

• Knowledge of material and process variability analysis.

• Skilled in root-cause analysis (8D, Fishbone, 5 Whys).

• Competence in data management, test result interpretation, and reporting.

• Strong sense of integrity and independence — ability to say “stop” when needed.

Soft Skills

• High attention to detail and process discipline.

• Excellent communication with technical and production teams.

• Confidence and authority to make quality decisions under pressure.

• Structured and calm approach to problem-solving.

• Strong leadership — developing inspectors and technicians through coaching.

• Safety-conscious and methodical.