Associate Manufacturing Engineer
Job in
Puerto De Luna, Guadalupe County, New Mexico, USA
Listed on 2026-07-22
Listing for:
Johnson & Johnson MedTech
Full Time
position Listed on 2026-07-22
Job specializations:
-
Engineering
Process Engineer, Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
Job Function
Supply Chain Engineering
Job Sub FunctionManufacturing Engineering
Job CategoryScientific/Technology
All Job Posting LocationsAnasco, Puerto Rico, United States of America
Job DescriptionJohnson & Johnson is currently seeking an Associate Manufacturing Engineer to join our team located in Añasco.
Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Responsible for all process/equipment validations and support product transfers. Adheres to environmental policy, procedures, and supports department environmental objectives.
Responsibilities- Initiates and completes technical activities to new or improved products or processes, for current programs, next generation programs and to meet strategic goals and objectives of the company.
- Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.
- Incorporates business policies and procedures into task completion. Understands the business needs of the company and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends.
- Cultivates internal and external network of resources to complete tasks. Serves as a resource in the training of new engineers and employees.
- Interacts cross‑functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters. Acts as spokesperson to customers on business unit current and future capabilities.
- Interfaces with Quality and Research and Development organizations to integrate new products or processes into the existing manufacturing area.
- Monitors performance of equipment, machines, and tools and corrects equipment problems or process parameters that produce nonconforming products, low yields or product quality issues.
- Drives 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 to ensure increase production outputs and increase operation team capabilities.
- Bachelor’s degree in Engineering is required
- 0‑2 years of experience in Engineering is preferred
- Experience in Medical Device or Pharmaceutical industry is preferred
- Knowledge on Statistics is desired
- Computer literate
- Good communication skills
- Fluent in English and Spanish
- Good interpersonal skills
- Experience or knowledge on problem solving/root cause analysis
- Understanding of regulatory compliance with all local and federal agencies i.e., FDA, ISO, OSHA, etc.
- Basic knowledge on Lean & Sigma methodologies. Certification is a plus
Position Requirements
10+ Years
work experience
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