era.
Si desea saber un poco más sobre esta ocasión, o está considerando presentar su candidatura, por favor, lea la siguiente información del puesto.
Requis

nica.
Se val

ional

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TECHNICAL OFFICE ENGINEER - PHARM

A SECTOR
Engineer with a mixed profile, capable of developing studies and detail engineering while simultaneously conducting technical project follow-up during execution to guarantee that the design is materialized with the required level of quality and s

tandards.Essential Requirement (Pharm a Sector) It is essential to provide demonstrable experience in projects within the pharmaceutical sector (production plants, laboratories, GMP areas, cleanrooms, critical utilitie

-

- ffice PhaseDevelop technical studies, reports, specifications, and project d

- efinitions.Design installations and systems (HVAC, utilities, processes, cleanrooms, etc.) in regulated en

- vironments.Elaborate basic and detailed executive e

- ngineering.Draft and review technical documentation: drawings, calculations, P&IDs;, layouts, equipment lists

- , URS, etc.Define technical criteria and design standards aligned with GMP/GxP regulations and client re

- quirements.Coordinate with multidiscipli

- nary teams.Ensure overall technical consistency of the project prior to the execu

- ng ExecutionProvide technical support to the site manager/construction manager regarding the devel





- oped design.Validate that execution aligns with the executive design and defined technic

- al criteria.Review technical solutions proposed on-site and evaluate their impact on quality, regulations, and

- performance.Analyze and validate technical changes (where applicable), ensuring document t

- raceability.Conduct occasional site visits to verify construction criteria and installat

- ion quality.Support testing, commissioning, and technical coordination with validation when required by

the project.

-

- Requirements:Technica l Background.Technical Engineering or Bachelor’s Degree in Engineering (Industrial, Mechanical, Electrical, Chemical,

- or similar).Previous experience in pharmaceutical sector projects (GMP/regulated

- environment).Experience in installation design and detailed engineering

- development.Ability to interpret and prepare technical drawings and d

- ocumentation.Knowledge of applicable regulations and good documentation practices (GDocP) in regulated

- environments.Rigorous, analytical, and quality-orie

- nted profile.Cross-functional coordination skills with site and technical

office teams.
Desirable /

-

- Valued Assets:Experience in cleanrooms and critical utilities (WFI, PW, clean steam, HVAC, spe

- cialty gases).Knowledge of GMP, GxP, EHS, and validat

- ion processes. xhfqzwm Experience in EPCM environments or tur

- nkey projects.Proficiency in AutoCAD and/or BIM

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📌 Ingeniero/A Oficina Técnica - Sector Farma (Barcelona)
🏢 FredLab
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