Responsibilities :
- Creating and updating detailed technical drawings and plans for various aspects of the facility.
- Maintaining accurate versions and revisions of drawings for traceability and project documentation. This could include: Architectural drawings: Floor plans, elevations, and sections of buildings and facilities within the site, including cleanrooms, laboratories, manufacturing areas, and utility spaces.
Mechanical drawings
Electrical drawings
Process equipment layouts
Utility systems - Compliance with regulations: Ensuring that all drawings and plans comply with regulatory requirements and industry standards for bio pharmaceutical manufacturing facilities, including Good Manufacturing Practices (GMP) and other relevant guidelines.
- Overall, translating conceptual designs and technical requirements into detailed drawings that guide the construction, installation, and operation of a bio pharmaceutical manufacturing site.
- Creating detailed technical drawings and plans using computer-aided design (CAD) software.
- Interpreting and translating rough sketches, specifications, and requirements into accurate and precise drawings.
- Collaborating with engineers to understand project requirements and objectives.
