TECHNICAL OFFICE ENGINEER - PHARM
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An engineer with a mixed profile, capable of developing studies and detailed engineering while simultaneously conducting technical project follow‑up during execution to guarantee that the design is materialized with the required level of quality and standards. Essential requirement: experience in projects within the pharmaceutical sector (production plants, laboratories, GMP areas, cleanrooms, critical utilities).
Responsibilities
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- Develop technical studies, reports, specifications, and project definitions.
- Design installations and systems (HVAC, utilities, processes, cleanrooms, etc.) in regulated environments.
- Elaborate basic and detailed executive engineering.
- 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 requirements.
- Coordinate with multidisciplinary teams.
- Ensure overall technical consistency of the project prior to execution.
- Provide technical support to the site manager/construction manager regarding the developed design.
- Validate that execution aligns with the executive design and defined technical 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 traceability.
- Conduct occasional site visits to verify construction criteria and installation quality.
- Support testing, commissioning, and technical coordination with validation when required by the project.
Requirements
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- Technical 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 documentation.
- Knowledge of applicable regulations and good documentation practices (GDocP) in regulated environments.
- Rigorous, analytical, and quality‑oriented profile.
- Cross‑functional coordination skills with site and technical office teams.
Desirable Assets
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- Experience in cleanrooms and critical utilities (WFI, PW, clean steam, HVAC, specialty gases).
- Knowledge of GMP, GxP, EHS, and validation processes. xqbhyrx
- Experience in EPCM environments or turnkey projects.
- Proficiency in AutoCAD and/or BIM.
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📌 Ingeniero/a Oficina Técnica - Sector Farma (Vic)
🏢 FredLab
📍 Vic