This biotech client develops projects starting from project definition and scope up to and including start-up in production, after which the new installations are handed over to production & maintenance. They are in need of a CQ Engineer (Utilities) to join their team ASAP!
Being part of the Engineering team means being central within the organisation and having a high exposure; from the work floor to the site leadership team!
Start Date: ASAP - end of year. Must be freelancer.
You are a member of the engineering team for clean and black utilities that is working on the Z900 project. The project is part of the expansion strategy of the company for an increase of product capacity and is now at the start of the construction phase. As CQ engineer you will be responsible for:
- Writing SAT documents in order to perform the commission of skids, systems and/or packages
- Writing IQ/OQ/PQ documents and perform the qualification
- Carry out validation tests and commissioning.
- You ensure a complete as-built file and handover of the project to the internal customers production and maintenance.
Send your CV to email@example.com to discuss further!
You ensure a transparent, fluent and effective communication with all internal stakeholders as well as with external partners (suppliers, contractors, engineering companies, etc.).
Profile:Bachelor with min. 5 years experience or master degree electro-mechanics or process Knowledge of project management systems and tools (eg MS Office, MS Project) Experience developing projects in a production environment Knowledge of cGMP procedures, Good Documentation Practise (GDP), EMA/FDA requirements & risk management tools HAZOP/FMEA Experience in Pharmaceutical manufacturing, process validation, equipment qualification. Knowledge of piping systems and understanding of PID’s You speak and write fluent English, Dutch and/or French