Engineering Quality Engineer

Il y a 20 heures

Zaventem, Vlaanderen, Belgique Asco Temps plein

Company Introduction :

ASCO, part of Swiss group Montana Aerospace, began operations as a private subcontractor in 1954.

Today ASCO Group is engaged in a broad range of development, engineering, manufacturing and assembly activities providing multidisciplinary subcontracting services to various markets and aerospace programs around the world.

Asco operates from several locations, Belgium, Canada, Germany and USA, with a turnover exceeding 340 million euros.

Asco produces over 2,500 assemblies every month and has the ambition to be a world leader in design and manufacture of high lift devices, complex mechanical assemblies and major functional components for the aerospace industry.

Montana Aerospace AG is a highly-vertically integrated manufacturer and supplier of system components and complex assemblies for the aerospace, e-mobility and energy sectors with worldwide engineering and manufacturing operations has acquired 100% of the share of the Asco Group beginning of April 2022.

Asco is now looking for an EQ Engineer (Engineering Quality Engineer) who performs full or partial first article inspections (FAIs) to validate process stability and capacity prior to series production, and validate manufacturing routings, operator instructions (ATS) and control plans.

Responsabilities :

1. Carrying out FAI : First Article Inspection

 Carry out and validate FAI, DVI, EFAE and DVE files in accordance with approved AQIs and customer documents.

Perform product/process FAI on new products.Perform FAI deltas (validation of changes at the engineering definition or process level).

2. Validation of control plans

Perform an assessment to validate the control plan (CP) in accordance with approved APIs and AQIs.

Validate the CPs for all manufactured parts, including those involved in machining and assembly processes.Validate the CPs of deltas as part of changes made (at the engineering definition or process level).

3. Validation of routings and Asco Technical Sheets (ATS)

Conduct an assessment to validate the routings in accordance with the approved APIs.

Validate routings for all manufactured parts.Validate changes made to routings (change management process).Validate ATS (Asco Technical Sheets) for polishing and assembly (except for special processes outside the scope of EQ).

4. Validation of Asco Control Cards (CC)

Conduct an assessment to validate control cards in accordance with approved APIs and AQIs.

Validate CCs for all manufactured parts, including those involved in machining and assembly processes.Validate CCs for deltas as part of changes made (at the configuration or process level).

5. Review of customer requirements


Participate in the Customer Requirement Review to ensure that the project team fully understands and has comprehensively covered the customer's requirements.

Verify that the content of the plans is correct, complete, clear (no room for interpretation) and measurable.Identify any clarification, correction and/or deviation requirements to Customer Quality.Initiate, carry out or organise & analyse 2D/3D comparisons where necessary and monitor the implementation of any necessary corrections.

6. Creation of Control Plans

Create Control Plans to define a comprehensive and efficient inspection process based on customer requirements (plans and specifications) defined in the configuration

Define with the technical team which parameters can be controlled by the process in parallel with the definition of the processWhen not guaranteed by the process, define (in collaboration with the Method Agent for production control cards) when to control (production, Manual QC, CMM, Final QC), how to control (including the definition of the measuring instrument) and the frequency of measurement based on the inspection strategyDefine a reliable and economical means of inspecting parts.Keep control plan revisions under control.Obtain validation from an Engineering Quality Engineer from the Engineering Quality & Validation group

7. Validate CMM programs and control tools.

Validate CMM programs and control tools to ensure deliverables comply with requirements.

Validate CMM programs in accordance with the criteria defined in the proceduresValidate control tools defined in Control Plans and designed by Fixture Design.Initiate and organise, in cooperation with CQE, MSA (GRR) studies for the identified measurement equipmentObtain validation of Control Charts by an Engineering Quality Engineer from the "Engineering Quality & Validation" group

8. PFMEA / SPC

 Participate in PFMEA activities in order to proactively prevent an