United Pharma Technologies Inc
Computer Aided Design Technician
United Pharma Technologies Inc, Baltimore, Maryland, United States
We are seeking an experienced CAD Technician with a strong background in pharmaceutical and GMP-regulated facilities. The candidate will support engineering, validation, and facility teams by developing and maintaining accurate CAD drawings for cleanrooms, utilities, process equipment, and manufacturing layouts in compliance with regulatory and industry standards.
Key Responsibilities
Develop, modify, and maintain 2D/3D CAD drawings for pharmaceutical manufacturing facilities, laboratories, and cleanroom environments.
Prepare layouts for process equipment, utilities (HVAC, piping, electrical, plumbing), and instrumentation.
Support GMP-compliant facility design including classified areas, material/personnel flow, and contamination control.
Update as-built drawings based on field changes and engineering markups.
Collaborate with engineering, validation, maintenance, and project teams during facility upgrades and expansions.
Ensure drawings comply with cGMP, FDA, ISO, and ASME standards.
Manage drawing control and documentation in accordance with change management and document control procedures.
Support commissioning, qualification, and validation activities by providing accurate drawings for IQ/OQ/PQ documentation.
Participate in design reviews and provide technical drafting support during audits and inspections.
Seniority Level Mid-Senior level
Employment Type Contract
Job Function Pharmaceutical Manufacturing
Location: Suitland, MD
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Key Responsibilities
Develop, modify, and maintain 2D/3D CAD drawings for pharmaceutical manufacturing facilities, laboratories, and cleanroom environments.
Prepare layouts for process equipment, utilities (HVAC, piping, electrical, plumbing), and instrumentation.
Support GMP-compliant facility design including classified areas, material/personnel flow, and contamination control.
Update as-built drawings based on field changes and engineering markups.
Collaborate with engineering, validation, maintenance, and project teams during facility upgrades and expansions.
Ensure drawings comply with cGMP, FDA, ISO, and ASME standards.
Manage drawing control and documentation in accordance with change management and document control procedures.
Support commissioning, qualification, and validation activities by providing accurate drawings for IQ/OQ/PQ documentation.
Participate in design reviews and provide technical drafting support during audits and inspections.
Seniority Level Mid-Senior level
Employment Type Contract
Job Function Pharmaceutical Manufacturing
Location: Suitland, MD
#J-18808-Ljbffr