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Line Walkers - Belgium

4 open positions

Our client is Europe’s leading provider of construction solutions, delivering complex engineering and construction projects for the world’s leading corporations across sectors including enterprise and hyperscale data centres, advanced technology and life sciences, and fire protection - powered by innovative people and a supportive culture that helps everyone reach their full potential.

 Overview

Support the site Quality team by performing systematic line walkdowns and installation verification across process piping, utilities, HVAC, and equipment installation. Working to the QCRs, you will verify installation readiness at W1 and W2 stages and help drive right‑first‑time closeout on a regulated pharmaceutical construction project in Belgium.

 Key Responsibilities

  • Perform line walkdowns and verify installation against drawings/specifications, work packs, and project SOPs (process pipe, utility pipe, HVAC, and equipment installs)
  • Verify installation at W1 and W2 stages (as defined by the project) and confirm readiness for inspection/testing/turnover activities
  • Identify punch items/defects, record findings clearly, and coordinate with trades/subcontractors for right‑first‑time closeout
  • Support QCRs by prioritising daily walkdowns, managing area readiness, and confirming prerequisites are in place before formal inspection points
  • Verify housekeeping, labelling/ID, protection of installed systems/equipment, and basic traceability requirements expected on regulated sites
  • Maintain walkdown records and provide accurate status updates to QCRs/QA/QC to support audit‑ready turnover documentation

Key Interfaces

  • Reports to: QCR(s) / Site QA/QC team lead
  • Works closely with: construction supervision, subcontractor foremen, commissioning/turnover teams, and discipline engineers

Requirements

  • Experience in piping/mechanical/HVAC walkdowns, QA/QC support, commissioning support, or construction completion roles on industrial projects
  • Able to read drawings/isometrics and understand installation completion requirements and checklists
  • Strong attention to detail and confident recording/communicating punch items and readiness status
  • Comfortable working in a regulated environment with high documentation standards (pharma/life sciences preferred)
  • Site-based availability in Belgium and ability to work across multiple disciplines/areas

 Location – Belgium

Contract Duration – 18 Months

--Awilli Group AG--

Weld Inspectors

3 open positions

Our client is Europe’s leading provider of construction solutions, delivering complex engineering and construction projects for the world’s leading corporations across sectors including enterprise and hyperscale data centres, advanced technology and life sciences, and fire protection - powered by innovative people and a supportive culture that helps everyone reach their full potential.

 Overview

Provide independent on-site oversight of subcontractor welding (fabrication and installation) on a major pharma construction project in Belgium. Verify compliance with approved procedures/specifications and confirm inspection coverage, traceability, and audit-ready records. Work closely with QCRs and the QA/QC Manager to keep weld quality “right first time.”

Key Responsibilities

  • Oversee subcontractor welding activities (shop and field) to approved WPS, specifications, drawings, and site SOPs
  • Coordinate with QCRs to set daily inspection priorities and manage hold/witness points
  • Verify subcontractor QC effectiveness (ITP adherence, inspection/NDT coverage, weld maps, traceability) and escalate gaps promptly
  • Review/validate weld documentation (weld maps, VT/NDT reports, material/consumable traceability, redlines/as-builts as applicable)
  • Support NCR, punch and rework closeout by confirming corrective actions and evidence are complete
  • Support walkdowns/line checks and turnover readiness in coordination with QA/QC and commissioning teams

Key Interfaces

  • Reports to: Client/Owner Quality Lead or Site QA/QC Lead (day-to-day via QA/QC Manager/QCRs as agreed)
  • Works closely with: QCRs, QA/QC Manager, subcontractor QC/inspection teams, construction supervision, and commissioning/turnover teams

Requirements

  • Weld Inspector experience on industrial construction projects (pharma/life sciences preferred)
  • Strong knowledge of weld QC/inspection, ITPs, and hold/witness points
  • Familiar with traceability and closeout documentation (weld maps, VT/NDT records, material certificates)
  • Clear communicator with a proactive, fact-based approach to escalation and issue closure
  • Able to work in a fast-paced site environment across multiple subcontractor interfaces

 Location – Belgium

Contract Duration – 18 Months

--Awilli Group AG--

Quality Control Representative

2 open positions

Our client is Europe’s leading provider of construction solutions, delivering complex engineering and construction projects for the world’s leading corporations across sectors including enterprise and hyperscale data centres, advanced technology and life sciences, and fire protection - powered by innovative people and a supportive culture that helps everyone reach their full potential.

 Overview

Hands-on site quality role ensuring installation work meets approved drawings/specs, project SOPs, and GMP / EU GMP expectations, supporting an audit‑ready regulated facility in Belgium/EU.

 Key Responsibilities

  • Verify construction/installation against drawings/specs, SOPs/quality procedures, and GMP requirements.
  • Perform routine inspections/walkdowns; confirm installations are complete and inspection-ready.
  • Drive right-first-time fixes with trades/subcontractors; escalate recurring/critical issues.
  • Maintain QC records/reports/checklists and support testing, CQV / Validation interfaces, commissioning, and turnover readiness with complete, audit‑ready documentation.

Requirements

  • QC/site inspection experience on construction projects (trade background a plus).
  • Experience in pharma/life sciences/cleanroom or other regulated industrial environments.
  • Working knowledge of SOP-driven execution, GMP / EU GMP-controlled areas, and construction quality standards.
  • Familiar with ITPs, punch/snag closeout, and basic turnover documentation.

Key Skills & Attributes

  • Strong eye for detail and workmanship; practical, site-first mindset.
  • Clear communicator; able to challenge non-conformances respectfully and drive closure.
  • Understands inspection readiness, testing handoffs, and documentation expectations

 Location – Belgium

Contract Duration – 18 Months

--Awilli Group AG--

QA Manager - UK

1 open position
We are seeking an experienced Quality Manager to oversee all QA/QC activities on a major industrial construction project the UK.
The successful candidate will be responsible for ensuring that all construction, fabrication, and installation works are completed in accordance with project specifications, industry standards, and regulatory requirements.
Key Responsibilities
Lead and manage the site QA/QC team
Develop and implement the Project Quality Plan (PQP)
Ensure compliance with:
ISO 9001 standards
Client specifications and ITPs (Inspection Test Plans)
Coordinate and oversee:
Weld inspections (WPS/PQR compliance)
NDT activities (RT, UT, MPI, DPI)
Mechanical and piping inspections
Manage material traceability and certification (MTRs)
Conduct internal and external audits
Liaise with:
Client representatives
Third-party inspectors
Engineering and construction teams
Control and maintain all quality documentation and turnover dossiers
Identify non-conformances (NCRs) and drive corrective actions
Support commissioning and handover phasesRequirements
Proven experience as a QA/QC Manager / Quality Manager on:
Industrial / pharmaceutical / chemical / oil & gas projects
Strong knowledge of:
Welding standards (ASME / EN / ISO)
Piping & mechanical systems
Experience managing ITPs, QA systems, and audits
Familiar with site documentation control systems
Excellent communication and leadership skills
Ability to work in a fast-paced, live construction environment
Qualifications (Preferred)
Degree or trade background in Mechanical / Engineering
CSWIP 3.1 / 3.2 or equivalent (advantageous)
ISO 9001 Lead Auditor (preferred)
Experience on COMAH / high-hazard sites (big plus)
--Awilli Group AG--

Mechanical Piping Supervisor – Semiconductor Industry

1 open position

Could you please arrange to run job adverts for the attached Mechanical Supervisor position within the semiconductor industry? We are looking to target candidates with experience in bulk gas and specialty gas systems.

Ideally, we would like the adverts to be promoted in the following locations:

  • Singapore
  • Malaysia
  • India

The role requires a minimum of 5 years’ experience within the semiconductor industry, with strong experience overseeing both prefabrication work in workshop


Job Advertisement:

Mechanical Supervisor – Semiconductor Industry

 


The Mechanical Supervisor is responsible for managing and supervising mechanical installation works within semiconductor manufacturing facilities, with a strong focus on bulk gas and specialty gas systems. The role involves coordinating site activities, overseeing prefabrication works in the workshop, and ensuring the project site is fully prepared for installation activities. The Mechanical Supervisor will act as a key point of contact for the client and ensure works are delivered safely, efficiently, and to the highest quality standards.

 

Key Responsibilities

 

·        Client Interface                

Act as the primary point-to-point contact between the client and the mechanical installation team, ensuring clear communication, progress updates, and prompt resolution of technical or operational issues.

·        Site Supervision                

Supervise day-to-day mechanical installation activities on site, ensuring all works are completed safely, on schedule, and in line with project specifications and standards.

·        Bulk Gas Systems            

Oversee the installation and coordination of bulk gas systems including distribution piping, storage systems, manifolds, and associated infrastructure.

·        Specialty Gas Systems

Supervise the installation of high purity and specialty gas systems used within semiconductor manufacturing environments, ensuring compliance with project and client requirements.

·        Prefabrication Oversight

Coordinate and oversee prefabrication activities in the workshop, including fabrication of pipe spools, modular racks, and mechanical assemblies to ensure readiness for site installation.

·        Site Preparation

Ensure the project site is properly prepared for installation activities including layout verification, material readiness, equipment access, and coordination with other trades.

·        Planning and Coordination

Work closely with project managers, engineers, QA/QC personnel, and other supervisors to ensure installation activities align with project schedules and milestones.

·        Quality Assurance

Ensure all mechanical works comply with approved drawings, P&IDs, isometrics, and project quality standards. Support QA/QC inspections and system walkdowns.

·        Safety Compliance

Promote and enforce strong safety practices on site, ensuring all activities are carried out in accordance with site safety procedures, permit systems, and HSE policies.

·        Team Leadership

Lead and manage mechanical crews including pipefitters, welders, and installers, ensuring productivity and high standards of workmanship.

·        Project Reporting

Provide regular progress updates, identify potential risks or delays, and coordinate corrective actions to maintain project schedules.

·        Commissioning Support

Assist with system testing, pressure testing, flushing, and handover to commissioning teams.

 

Experience and Qualifications

 

·        Minimum 5 years’ experience working within the semiconductor industry

·        Strong experience with bulk gas systems and specialty gas systems installation

·        Experience overseeing prefabrication works in fabrication workshops

·        Experience preparing and coordinating site installation activities

·        Ability to read and interpret P&IDs, isometrics, and technical drawings

·        Experience working in cleanroom and high-specification environments

·        Strong leadership, organisational, and communication skills

·        Key Systems Experience

·        Bulk gas distribution systems

·        Specialty and high purity gas systems

·        High purity stainless steel piping systems

·        Orbital welding and semiconductor piping standards

·        Gas cabinets, valve manifold boxes (VMBs), and regulators

·        Cleanroom mechanical installations

 

--Awilli Group AG--

Compliance Labour Manager

1 open position

Belgium | Project-based

Join our project team and keep a major pharma build compliant from day one.

Duration: 12 month contract

Overview

Own workforce compliance and site access for a regulated pharmaceutical construction project in Belgium - mobilisation, LIMOSA posted-worker declarations, A1/right-to-work documentation checks, GMP site induction, and audit-ready records across multiple contractors.

Key responsibilities

  • Run GMP site inductions and access control for all personnel (employees, contractors, and visitors) before first entry
  • Approve site entry and validate eligibility documentation, including LIMOSA declarations and A1 certificates where applicable
  • Verify A1 / right-to-work documentation, visas, and work authorisations (Belgium/EU) and ensure they are in place prior to access
  • Ensure employment, tax, and posted-worker compliance; maintain audit-ready onboarding and access records for all contractors

Required experience

  • Compliance experience on construction/industrial projects (regulated sites preferred)
  • Knowledge of employment, immigration, and posted-worker compliance in Belgium/EU (including LIMOSA and A1 documentation)
  • Able to manage multinational workforces and multiple subcontractors

Desirable

  • Pharma/life sciences or cleanroom project experience
  • Familiarity with Belgian/EU posted-worker frameworks (LIMOSA), A1 requirements, and GMP site induction expectations

Why it matters

Reduces regulatory and tax risk, prevents mobilisation delays, and keeps the project audit-ready in a highly regulated environment.

 


--Awilli Group AG--