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Project engineer Capex - Life Sciences - M/V/X

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Vacancy details

General information

RECRUITMENT (logo)

Publication date

20/08/2025

Position description

Category

OPERATIONS - ENGINEERING/PRODUCTION

Job title

Project engineer Capex - Life Sciences - M/V/X

Contract

Permanent contract

Job description

Project Engineering & Control

- Prepare cost estimations & conduct Value Improvement Reviews

- Perform project risk assessments

- Prepare project initiation documents (Business Requirements – PBR, Work Breakdown Structure – WBS, Cost Breakdown Structure – CBS, Project Scope Statement – PSS)

- Develop project sourcing strategy

- Identify technical solutions

- Draft project quality plan

- Prepare project procurement plan, manage tenders, and purchasing

- Manage project HSE and conduct safety reviews

- Conduct project reviews (e.g., Technical Quality Review – TQR, constructability)

- Develop commissioning plan/strategy

- Set up Project Change Management and handle changes

- Submit legal permits for the project

- Prepare equipment specifications and system requirements (e.g., - - User Requirements Specification)

- Develop project execution plan (e.g., construction phase)

- Prepare/execute project health & safety risk assessments (equipment/process)

- Prepare functional specifications

- Draft, review, and approve drawings, lists, schedules, diagrams, layouts, calculations, and datasheet

- Issue orders/contracts based on technical specs and bill of quantities

 

Monitor and manage project vendors/contractors/third parties

Develop test specification/plans for commissioning & qualification

Execute construction management and installation supervision

Perform FAT/SAT/inspections of new equipment

Implement and monitor safety and inspection plans for contractors

Execute work orders according to procedural instructions

Carry out commissioning activities

Manage project deficiencies and deviations

Develop and execute the project strategy based on customer needs (cost, schedule, functionality, quality

Re)Qualification

Develop qualification plan

Perform GMP risk assessments (incl. Sensor Risk Assessment – SRA)

Create DQ, IQ, and OQ protocols

Execute DQ, IQ, and OQ

Draft DQ, IQ, and OQ reports

Provide technical troubleshooting during PQ and validation

Business Industry

Life sciences

Profile

Relevant Experience:

5 years of technical experience, including 2 years in capital investment projects in the chemical or pharmaceutical industry

Leadership experience managing external resources

Proven project management skills, including contract management and project control

Broad interdisciplinary knowledge

Extensive HSE and GxP/QA knowledge

 

Education & Qualifications:

Degree in Engineering (Dipl. Ing. / M.Sc. / B.Sc.) or equivalent

 

Languages:

Fluent in English and proficient in the local language

Position location

Job location

Europe, Belgium, Flanders, Antwerp

Location

Puurs

Candidate criteria

Level of experience

3 to 5 years


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