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Designer draftsman in AutoCAD
We are looking for a Project Draftsman in AutoCAD with experience in technical drawing and design of facilities for the pharmaceutical industry in a GMP environment, to join our team to collaborate in the design, review and development of technical project plans.
Main functions
- Preparation of distribution plans, P&DS, Piping, Layout de Salas, Technical Furniture and Facilities.
- Update and modification of plans according to project phases.
- Plan database management.
- Interpretation of mechanical planes, electrical schemes, HVAC principle and architecture schemes.
- Coordination with project engineers and execution responsible.
- Control and organization of technical documentation.
- Participation in technical visits for data collection.
- Make measurements and listings of materials.
REQUIREMENTS THAT YOU HAVE TO MEET
- Imprescindible Autodesk AutoCAD, MS Word y MS Excel.
- Minimum formation: FP II / CFGS in mechanical delineation, development of mechanical projects or equivalent.
- Autonomous, detailed, orderly, quality and deadlines.
- Intermediate English (interpretation of technical documentation).
- Own vehicle.
We will value
- Clean's Design Experience (purified water ties, wfi, pure steam, sip, cyp, gases).
- Air principle schemes in clean rooms.
- Experience in projects in the pharmaceutical industry sector.
- Experience in aseptic process.
- Experience under GMP standard.
- Knowledge of the Asme BPE standard.
- Knowledge of SolidWorks, Autodesk Revit, BIM.
What do we offer
- Stable contract with Professional Development Plan.
- Participation in relevant projects for the pharmaceutical sector.
- Flexible schedule and possibility of partial teleworking (according to project).
- Internal training and possibility of expanding responsibilities.
- Competitive salary according to profile + diets.
Qualifications technician
We are looking for a qualifications technician that actively participates in qualification projects of equipment, rooms and auxiliary facilities and control system, both in office and in the field.
Main functions
- Preparation and execution of qualification documents, USA, RA, FS, VP, DQ, IQ, OQ, PQ.
- FAT and SAT assistance.
- Qualification of equipment and facilities in GMP environment.
- Documentary review and traceability according to regulatory requirements.
- Drafting reports and document closure of the project.
- Coordination with customers and technical assistance in their facilities.
- Technical Training: CFGS in manufacture of pharmaceutical and related products, quality analysis and control laboratory, electronic maintenance or industrial mechatronics or degree in engineering, pharmacy or similar. Profiles with technical cycles that have worked in GMP environments or with experience in team qualification will also be assessed.
- Valuable Experience in qualification/validation projects.
- GMP regulations knowledge (GAMP5, FDA) will be valued.
- Management of office tools and technical writing software.
- Intermediate English level (B2).
- Methodic, proactive and quality orientation.
- Own vehicle.
What do we offer
- Stable contract with Professional Development Plan.
- Participation in relevant projects for the pharmaceutical sector.
- Flexible schedule and possibility of partial teleworking (according to project).
- Internal training and possibility of expanding responsibilities.
- Competitive salary according to profile + diets.
Send us your CV
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