Jobs

Legal Inspection Engineer

Discipline
Engineering
Sector
Life Science
Location
Vlaams-Brabant
Vacancy ID
59186

Responsibilities

  • As a Legal Inspection Engineer you support process safety risk assessments.
  • You support customers to deploy mitigation plans for Process Safety High Severity Risks
  • You are individually or as part of a project team responsible for the inspection of electronic, mechanical, HVAC and utilities equipment and related products such as safety devices, pressure equipment, piping...
  • You support the following activities in the frame of projects: PID reviews,fluid list consolidation, Inspection Master Plan (IMP) and conformity assessment.
  • You determine Minimum Legal File, verify safety devices design and calculation notes.
  • You participate to Risk Analysis (based on Equipment Directive) for assembly.
  • You participate on start-up phase prior to Hand Over approval.
  • You approve decision tree made by Analyst to attest conformity and check robustness study. Decision tree is based on dimensional drawing, construction code, non destructive control and hydraulic test. Animate Risk Analysis (Kinney) with user and EHS representatives to support decision (economic efficiency of replacement or making conformity assessment).
  • You are resonsible for request Technical Modification (study) or issue Notification when non conformity is not covered by project.
  • You support to periodic inspection scheduling (intern and external visits, check valves calibration). Establish, in collaboration with Notified Body inspector, exception to internal visit when not feasible. Support statistics on thickness inspection by ultrasonic waves or measures of boiler tubes deformation.
  • You support Risk Based Investigations (RBI) and determine most efficient inspection type taking into account customer constraints. Analyse results and revise frequency of controls (periodicity).
  • You lead L2 audit on pressirized.

Requirements

  • Electromechanical Engineer
  • Technical safety background
  • First experience in industry,pharma is prefereed
  • Perform his/her work in a cGMP consistent manner
  • Continuous improvement of technical background
  • Pragmatic and good communication skills
  • SAP
  • MS Office
  • Fluent in English and French
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