P&ID CAD Consultant

Planet Pharma; Hillerød; On-site; DKK 420,000 - 600,000; Full time

Job summary

Planet Pharma is seeking an experienced CAD Designer for P&ID drafting and document management in a regulated pharmaceutical setting. You will perform red-to-black updates in AutoCAD, maintain drawings, and ensure traceability through meticulous version control.

The role requires 5+ years of P&ID experience, strong CAD skills, and familiarity with document control and regulatory standards. Experience with Meridian or similar DMS is preferred.

Qualifications

• 5+ years’ experience in P&ID drafting and red-to-black updates.
• Proficient in AutoCAD and controlled engineering documentation.
• Solid understanding of P&ID symbols, equipment references, instrumentation, tags.
• Experience with document control and revision management.
• Ability to manage multiple drawing updates while ensuring traceability.
• Experience in pharmaceutical/regulated environments is advantageous.
• Experience with Meridian or similar DMS is preferred.

Responsibilities

• Perform P&ID blacklining based on approved engineering mark-ups.
• Execute red-to-black updates in AutoCAD per drawing standards and procedures.
• Create, revise and maintain engineering drawings and documentation.
• Review updated drawings for accuracy, completeness, consistency and legibility.
• Apply P&ID conventions, CAD standards and TAG numbering principles.
• Process technical review comments and implement changes.
• Maintain full traceability between source mark-ups, revisions and deliverables.
• Coordinate with engineering and document control to ensure timely project delivery.

Skills

P&ID drafting

AutoCAD

Documentation control

Traceability

Drawing standards

Regulatory environment

Multi-tasking

Education

Engineering technology diploma

Tools

Meridian (DMS)

CAD standards software

Job description

Contract l 9months l full-time

Responsibilities

• Perform P&ID blacklining based on approved engineering mark‑ups.
• Execute red-to-black updates in AutoCAD in accordance with drawing standards and procedures.
• Create, revise and maintain engineering drawings and associated documentation.
• Review updated drawings for accuracy, completeness, consistency and legibility.
• Apply P&ID conventions, CAD standards and TAG numbering principles.
• Process technical review comments and implement approved changes.
• Maintain full traceability between source mark‑ups, revisions and final deliverables.
• Coordinate closely with engineering and document control teams to ensure timely project delivery.

Requirements

• 5+ years’ experience in P&ID drafting, blacklining and red-to-black updates.
• Strong proficiency in AutoCAD and controlled engineering documentation.
• Solid understanding of P&ID symbols, equipment references, instrumentation, line types and TAG numbering systems.
• Experience reviewing engineering drawings for technical accuracy and compliance.
• Experience working within document control and revision management processes.
• Ability to manage multiple drawing updates while maintaining quality and traceability.
• Experience within pharmaceutical, biotech, life sciences or another regulated engineering environment is advantageous.
• Experience with Meridian or a similar engineering document management system is preferred.

Preferred Background

• Technical Designer
• Engineering Technician
• CAD Designer
• Architectural Technology
• Engineering Documentation Specialist