GMP Mechanical Designer for Biotech Equipment

Manus Bio Inc.; Augusta (GA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Opportunities for personal and professional advancement

Freedom to make critical decisions

Collaborative work environment

Job summary

A biotechnology company located in Augusta, Georgia, is looking for a Mechanical Designer to support the design and development of mechanical systems for biotech and pharmaceutical manufacturing. The ideal candidate will have a degree in Mechanical Engineering or a related field, with proficiency in AutoCAD 2D and 3D, and a basic understanding of GMP compliance. This role requires strong attention to detail and the ability to manage multiple deliverables in a regulated environment.

Qualifications

• 2–5 years of mechanical design experience; entry-level candidates with strong internship or co-op experience will be considered.
• Basic understanding of GMP requirements and design documentation practices in a regulated environment.
• Strong attention to detail and ability to manage multiple drawing deliverables concurrently.

Responsibilities

• Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in compliance with GMP and cGMP standards.
• Assist in the design of process equipment, piping systems, utility systems, and facility modifications for biotech/pharma manufacturing areas.
• Support mechanical design workstreams on capital projects from initiation through commissioning and qualification.

Skills

AutoCAD 2D

AutoCAD 3D

GMP compliance

Mechanical design

Attention to detail

GD&T

Education

Associate’s or Bachelor’s degree in Mechanical Engineering Technology, Mechanical Design, or related field

Tools

SOLIDWORKS

Inventor

Job description

A biotechnology company located in Augusta, Georgia, is looking for a Mechanical Designer to support the design and development of mechanical systems for biotech and pharmaceutical manufacturing. The ideal candidate will have a degree in Mechanical Engineering or a related field, with proficiency in AutoCAD 2D and 3D, and a basic understanding of GMP compliance. This role requires strong attention to detail and the ability to manage multiple deliverables in a regulated environment.