Staff Manufacturing Engineer, MedTech & Vision

Biopharma Careers

Añasco (PR)

On-site

USD 90,000 - 120,000

Full time

14 days+
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Job summary

Johnson & Johnson Med Tech in Anasco, Puerto Rico, is recruiting for a Staff Manufacturing Engineer. This role, located in Añasco, PR, supports advanced engineering, design, and construction of manufacturing facilities, systems, and equipment, with cross‑functional collaboration across GMP/ISO environments.

Under Engineering Manager guidance, you will lead projects, perform cost analyses, ensure compliance, and drive continuous improvement in production and processing equipment.

Qualifications

  • Bachelor’s degree in Engineering required.
  • Minimum of 6 years in maintenance manufacturing, R&D, or process development.
  • Demonstrated project management experience.
  • Proven validation experience (FAT, IQ, OQ, PQ).
  • Fully bilingual: Spanish & English.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint).
  • Willingness to travel up to 10%.

Responsibilities

  • Develops process excellence techniques to identify systematic issues.
  • Leads projects/programs with high complexity ensuring safety and compliance.
  • Provides technical support to evaluate process changes and optimizations.
  • Defines engineering standards and mentors the group.
  • Manages project estimates, schedules, and costs.
  • Drives new ideas in incoming processes and coordinates with multiple sites.
  • Supports non-conformance investigations and corrective actions.
  • Maintains SOP, GMP, and regulatory compliance.
  • Writes and executes validation strategies.

Skills

Project Management
Bilingual Spanish & English
Microsoft Office
Data analysis (Minitab)

Education

Bachelor’s Degree in Engineering

Tools

Minitab

Job description

Johnson & Johnson Med Tech in Anasco, Puerto Rico, is recruiting for a Staff Manufacturing Engineer. This role, located in Añasco, PR, supports advanced engineering, design, and construction of manufacturing facilities, systems, and equipment, with cross‑functional collaboration across GMP/ISO environments.

Under Engineering Manager guidance, you will lead projects, perform cost analyses, ensure compliance, and drive continuous improvement in production and processing equipment.

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