Biotech GMP Mechanical Designer (On-Site)

Energy Jobline ZR; Aiken (SC); Vor Ort; USD 65.000 - 90.000; Vollzeit

Zusammenfassung

MR Lowcountry, LLC. in the Aiken, SC area seeks a Mechanical Designer to support 2D/3D designs and documentation for biotech/pharma facilities. You will work under senior engineers to ensure GMP compliance and accurate drawings.

The role emphasizes AutoCAD proficiency, collaboration with process and automation teams, and contributing to projects from concept through installation within a regulated manufacturing setting.

Qualifikationen

• Associate’s or Bachelor's degree in Mechanical Engineering Technology, Mechanical Design, or related field.
• 2–5 years of mechanical design experience; entry-level with strong/co-op experience considered.
• Proficiency in AutoCAD 2D and AutoCAD 3D; produce complete design packages independently.
• Basic understanding of GMP requirements and design documentation practices in a regulated environment.
• Working knowledge of GD&T, engineering calculations, and material selection.
• Strong attention to detail and ability to manage multiple drawing deliverables.

Aufgaben

• Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in GMP/compliant environments.
• Assist in design of process equipment, piping, utilities, and facility modifications for biotech/pharma areas.
• Produce and maintain engineering docs: P&IDs, layouts, BOMs, specs.
• Support design calculations, tolerance analyses, and material selections for cleanrooms.
• Review vendor drawings and verify equipment meets requirements.

Kenntnisse

Attention to detail

GMP awareness

Cross-functional collaboration

Communication skills

Ausbildung

Associate's or Bachelor's in Mechanical Engineering Technology or related field

Tools

AutoCAD 2D

AutoCAD 3D

SOLIDWORKS

Inventor

EDMS

Jobbeschreibung

MR Lowcountry, LLC. in the Aiken, SC area seeks a Mechanical Designer to support 2D/3D designs and documentation for biotech/pharma facilities. You will work under senior engineers to ensure GMP compliance and accurate drawings.

The role emphasizes AutoCAD proficiency, collaboration with process and automation teams, and contributing to projects from concept through installation within a regulated manufacturing setting.