Pharma Drafting & Documentation Coordinator

Techengpr

Carolina (PR)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

Technical & Engineering Consulting (T&E) seeks a Drafting Support & Coordinator to assist a major capital project in Carolina, PR. You will manage engineering drawings, revisions, and documentation in a regulated pharma/biotech setting, ensuring quality and timely workflows.

The ideal candidate offers a Bachelor's degree in engineering or related field, strong document control skills, and proven collaboration with cross-functional teams onsite.

Qualifications

  • Bachelor's degree in Engineering, Business Administration, Life Sciences, or related discipline.
  • Strong understanding of engineering document control and revision management processes.
  • Excellent organizational and time-management skills.

Responsibilities

  • Maintain, edit, and archive engineering drawings and related documentation in accordance with company standards and procedures.
  • Coordinate drawing revision and approval activities with engineering and project teams.
  • Lead and track drawing revisions to ensure timely completion in a fast-paced project environment.
  • Manage drafting-related reports and project coordination using company communication platforms.
  • Ensure documentation complies with applicable procedures, standards, and quality requirements.
  • Maintain all required customer training and qualifications.
  • Follow Lilly and T&E procedures to ensure quality and service continuity.
  • Provide additional drafting and project coordination support as needed.

Skills

Document control
Revision management
Time management
Communication
Organizational skills

Education

Bachelor's degree in Engineering or related field

Tools

Meridian GECMS
Microsoft Office

Job description

Technical & Engineering Consulting (T&E) seeks a Drafting Support & Coordinator to assist a major capital project in Carolina, PR. You will manage engineering drawings, revisions, and documentation in a regulated pharma/biotech setting, ensuring quality and timely workflows.

The ideal candidate offers a Bachelor's degree in engineering or related field, strong document control skills, and proven collaboration with cross-functional teams onsite.

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