Computer Aided Design Designer

Our client is seeking an experienced Senior CAD Designer to support onsite engineering and capital projects within a regulated pharmaceutical manufacturing environment. This role focuses on the creation, revision, and maintenance of high‑quality 2D CAD drawings for facilities, utilities, and production equipment while ensuring strict compliance with cGMP/GxP standards and site document control procedures.

The ideal candidate will work closely with engineering, project management, validation, and operations teams to deliver accurate, audit‑ready drawings across multiple concurrent projects.

• Develop, revise, and maintain 2D CAD drawings for facilities, utilities, and equipment using AutoCAD or equivalent tools
• Incorporate redlines, field markups, and as‑built updates into controlled drawings
• Ensure all drawings comply with cGMP/GxP requirements, site standards, and document control procedures
• Maintain drawing accuracy, consistency, revision history, and version control
• Support engineering and capital projects, including facility upgrades and equipment installations
• Collaborate with Engineering, Project Management, Validation, Quality, and Operations teams
• Manage multiple drawing packages simultaneously while meeting project deadlines
• Produce audit‑ready documentation suitable for regulatory inspections
• Clarify incomplete or ambiguous field information through effective communication

• 7+ years of CAD design experience in pharmaceutical, biotech, medical device, or other regulated manufacturing environments
• Strong proficiency with AutoCAD (2D) or equivalent CAD software
• Proven experience working with controlled drawings and document management systems
• Solid understanding of cGMP/GxP documentation practices, facility, utility, and equipment layouts, change control and revision management
• Ability to work independently with minimal supervision
• Strong attention to detail and organizational skills
• Excellent written and verbal communication skills

• Experience supporting onsite capital projects in pharmaceutical or biotech facilities
• Background in contract or project‑based roles
• Familiarity with as‑built documentation and field verification
• Experience producing documentation for regulatory audits and inspections

Mid‑Senior level

Contract

Pharmaceutical Manufacturing and Manufacturing