For a challenging experience in clean process piping, we are seeking an expert with expertise in the bio-pharmaceutical industry.
Clean process piping plays a vital role in the success of pharmaceutical development and manufacturing facilities. Our focus is on qualification to meet stringent industry rules and standards.
To ensure product quality requirements for our clients, we work on qualifying process piping systems that must meet criteria such as ASME-BPE codes and standards, design optimization for reliability, reducing waste, and ergonomic use. We also consider environmental requirements, safety, performance, and internal customer rules.
As an expert, you will work on engineering, design, and execution supervision of clean utilities distribution systems, clean utilities generation equipment, or any GxP equipment including CIP and SIP.
Your task will be to evaluate different alternatives or options for projects, specifying the most appropriate systems and equipment for user requirements. You will create process & instrumentation diagrams (P&IDs) and perform capacity calculations.
You should respect strict timing and define appropriate spare parts and specify instruments and regulation loops required. You will assist in completing alarm lists, datasheets, and other detailed design documents.
During the execution phase, you will supervise contractors and ensure correct implementation of designed systems. You will ensure client specifications and cGMP are respected throughout the project.
You will organize and follow system start-ups, ensuring their qualification.
Your Profile
1. Electromechanical Engineer, Mechanics, Industrial Chemist, or equivalent.
2. Perform multi-discipline engineering projects throughout their lifecycle, covering option development and evaluation, definition, estimating, design, procurement, construction, commissioning, qualification, and handover.
3. Coordinate different disciplines and project stakeholders to deliver on time, within budget, and to the required quality to meet customer needs.
4. Hold knowledge and experience in mechanical areas such as piping (to ASME BPE), rotating equipment, valves, pressure vessels, and atmospheric tanks, heat exchangers.
5. Have knowledge and experience of specialist areas such as ATEX, PED, Master-Data, sterility assurance.
6. Understand PIDs and schematic drawings.
7. Perform Factory Acceptance Tests (FAT) and Site Acceptance Test (SAT).
8. Write and execute IQOQ protocols.
9. Review and approve mechanical work packages such as engineering drawings (piping isometrics, P&IDs, and layout drawings) and schedules and Bills of Materials to issue onto the construction team.
10. Experience in the Bio-Pharmaceutical sector.
11. Ability to integrate and work in a team/communication.
12. Mastery of office automation tools.
13. Languages: English, French; Dutch is an advantage.
14. Stress resistance.