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Senior Manufacturing Engineer; One

Job in Puerto De Luna, Guadalupe County, New Mexico, USA
Listing for: Johnson & Johnson MedTech
Full Time position
Listed on 2026-08-28
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below
Position: Senior Manufacturing Engineer (One out of Two)
Location: Puerto De Luna

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at  As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Supply Chain Engineering

Job Sub Function

Manufacturing Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Anasco, Puerto Rico, United States of America

Job Description

Johnson & Johnson Med Tech, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Manufacturing Engineer. This position will be located in Añasco, Puerto Rico.

About Vision

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.

Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime. Your unique talents will help patients on their journey to wellness. Learn more at

Key Role Responsibilities
  • Leads and executes projects and/or programs of moderate to high level of complexity ensuring safety, regulatory compliance, company standards, operation requirements and business needs.
  • Drive the optimization of process output and throughput, equipment utilization, equipment downtime, waste reduction/yield improvements, budget management, standard cost, and capital investment management in a creative manner.
  • Provides technical support to peers and production areas in evaluating process deficiencies, process changes, modifications, and equipment failure. Defines, analyzes, reviews, and evaluates problems for prompt solutions.
  • Supports manufacturing in the day-to-day troubleshooting of equipment’s to ensure increase production outputs and increase operation team capabilities.
  • Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
  • Revise and maintain engineering, equipment’s, and process procedure.
  • Support the GMP audits as subject matter guide for product and processes.
  • Coordinates communications and interfaces within end users and machine manufacturers or suppliers.
  • Lead or participates in projects involving other departments and activities.
  • Evaluates process trends (Ex. Yield, OEE) to drive improvements of business results.
  • Daily monitoring and support to manufacturing lines
  • Provide training on process and validation requirements to operators and engineers
  • Stay in sync with all environmental, safety and occupational health policies
Qualifications Required Skills
  • Bachelor’s Degree in Engineering
  • Minimum of 4 years of experience is required in a maintenance manufacturing environment, R&D or Process Development
  • Proven experience with validation cycle (FAT, IQ, OQ and PQ)
  • Must be fully bilingual:
    Spanish & English
  • Proficiency with Microsoft Office:
    Word, Excel, Power Point
Preferred Skills
  • Preferred experience with data analysis tools:
    Minitab
  • Experience working at medical device industry or pharmaceutical preferred Experience in Project Management preferred
Other
  • This position will require up to 10% travel
  • The attendance policy for this requisition is Fully Onsite

At Johnson &…

Position Requirements
10+ Years work experience
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