CAD Documentation Lead
- North America, United States
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, a global Pharmaceutical manufacturing organization are looking for a talented CAD Documentation Lead to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.
Responsibilities:
- 3D Modeling and Design:
- Develop and maintain detailed 3D models of the project using SmartPlant 3D.
- Ensure all designs meet project specifications, industry standards, and regulatory requirements.
- Collaborate with engineering and design teams to create accurate and detailed design layouts.
- Documentation:
- Produce and manage comprehensive documentation for all project phases, including schematics, layouts, and detailed design drawings.
- Ensure all documentation is accurate, up-to-date, and easily accessible to relevant stakeholders.
- Create and maintain a centralized documentation repository for all project-related documents.
- Coordination and Collaboration:
- Work closely with project managers, engineers, and other stakeholders to gather and interpret project requirements.
- Coordinate with cross-functional teams to ensure seamless integration of design and documentation efforts.
- Assist in the review and approval process for design and documentation deliverables.
- Quality Control and Compliance:
- Perform quality checks on all documentation to ensure accuracy and compliance with project standards.
- Implement and enforce documentation standards and best practices throughout the project lifecycle.
- Ensure all designs and documentation comply with relevant regulatory and safety standards.
Requirements:
- Minimum of 5 years of experience in CAD documentation, with extensive experience using SmartPlant 3D.
- Education: Bachelor’s degree in Engineering, Design, or a related field preferred.
- Proficiency in SmartPlant 3D and other CAD software.
- Strong understanding of design principles, industry standards, and regulatory requirements.
- Excellent attention to detail and organizational skills.
- Ability to work collaboratively in a fast-paced, dynamic environment.
- Strong communication and interpersonal skills.
- Preferred Qualifications:
- Experience in the biopharmaceutical or CDMO industry.
- Familiarity with CAPEX projects and large-scale manufacturing facilities.
- Knowledge of additional CAD and design software tools.
If this role is of interest to you, please apply now!
#LI-NR1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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