Senior Biotech Equipment Designer (GMP/Pharma)

MRINetwork; Aiken (SC); On-site; USD 85,000 - 120,000; Full time

Job summary

MR Lowcountry, LLC in the Aiken, SC area is seeking a Senior Mechanical Designer to lead the development of mechanical systems for biotech/pharma manufacturing. This on-site role emphasizes detailed 2D/3D CAD work, piping and utility system design, and rigorous documentation in a regulated setting.

The ideal candidate brings 7+ years of GMP-regulated experience, strong AutoCAD skills, and a proven track record in cleanroom and sanitary applications.

Qualifications

• 7+ years of mechanical design experience in GMP-regulated biotech or pharma environments.
• Advanced proficiency in AutoCAD 2D and AutoCAD 3D (AutoCAD Mechanical or Plant 3D a plus).
• Experience designing process equipment, utility systems, or facility improvements in a manufacturing plant.
• Strong written and verbal communication skills; ability to produce clear technical documentation.

Responsibilities

• Develop detailed 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in compliance with GMP and cGMP standards.
• Design process equipment, piping systems, utility systems, and facility modifications for biotech/pharma manufacturing areas.
• Produce and maintain engineering documentation including P&IDs, equipment layouts, installation drawings, BOMs, and design specifications.
• Perform design calculations, tolerance analyses, and material selections for cleanroom and regulated environments.
• Lead mechanical design workstreams on capital projects from initiation through commissioning and handover.
• Collaborate with process, automation, quality, and facilities teams to align designs with requirements.

Skills

Mechanical design

AutoCAD 2D/3D

GMP/fda knowledge

Communication skills

Education

Bachelor’s degree in Mechanical Engineering

Tools

AutoCAD

SolidWorks

Inventor

Job description

MR Lowcountry, LLC in the Aiken, SC area is seeking a Senior Mechanical Designer to lead the development of mechanical systems for biotech/pharma manufacturing. This on-site role emphasizes detailed 2D/3D CAD work, piping and utility system design, and rigorous documentation in a regulated setting.

The ideal candidate brings 7+ years of GMP-regulated experience, strong AutoCAD skills, and a proven track record in cleanroom and sanitary applications.