Director, Pharmaceutical Process Design & Tech Transfer

IPS-Integrated Project Services; Cary (NC); On-site; USD 180,000 - 240,000; Full time

Job summary

IPS-Integrated Project Services is seeking a Director, Process Specialist to lead design and implementation of pharmaceutical manufacturing processes from pilot to full operation. The role drives process design, equipment selection, and strategy for GMP-compliant facilities.

You will manage client relationships, oversee scoping, and coordinate cross-disciplinary teams to ensure timely execution and adherence to industry standards. Travel is project-based and field-oriented.

Qualifications

• 15+ years of Process Design experience within the Pharmaceutical industry (OSD, Aseptic, or Biologics)
• Bachelor’s Degree from an accredited University or College in Engineering or relevant science
• GMP design experience
• Strong knowledge of process engineering codes and standards
• Active participation in industry organizations and client-facing engagements

Responsibilities

• Assesses project requirements and defines scope with the PM
• Writes scope of work for process and manufacturing
• Supports concept development and project design
• Prepares engineering studies and schematic design for new systems
• Documents process requirements and equipment lists
• Consults on tech transfer and process improvement
• Maintains relationships with clients and stakeholders
• Promotes design and production standards
• Coordinates document completion with clients and design teams
• Supports business development activities including proposals

Skills

Client leadership

Project management

Communication

GMP design

Process engineering

Education

Bachelor’s Degree in Engineering or relevant science

Tools

MS Word

MS Excel

PowerPoint

MS Project

Visio

Job description

IPS-Integrated Project Services is seeking a Director, Process Specialist to lead design and implementation of pharmaceutical manufacturing processes from pilot to full operation. The role drives process design, equipment selection, and strategy for GMP-compliant facilities.

You will manage client relationships, oversee scoping, and coordinate cross-disciplinary teams to ensure timely execution and adherence to industry standards. Travel is project-based and field-oriented.