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Manufacturing Engineer I

MG STAFFING GROUP
Posted 4 months ago, valid for 5 days
Location

Juncos, PR, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The job requires designing manufacturing processes and optimizing workflows to enhance efficiency and productivity.
  • Candidates should hold a Bachelor’s Degree in Engineering and have 0–3 years of experience in manufacturing or related fields.
  • Bilingual proficiency in English and Spanish is necessary, along with experience in Computer System Validation and working in regulated environments.
  • The position offers a salary of $75,000 per year and emphasizes compliance with FDA, ISO, and GMP regulations.
  • Applicants should possess strong organizational and communication skills, with knowledge of statistical tools and risk management being preferred.

Responsibilities may include the following: 

  • Design manufacturing processes, procedures, and production layouts for assemblies, equipment installation, machining, and material handling
  • Develop and optimize workflow and sequence of operations to improve efficiency and productivity
  • Design equipment and facility layouts to maximize production capabilities
  • Adapt machine and equipment designs to meet manufacturing and production requirements
  • Incorporate inspection and testing requirements into production processes
  • Evaluate equipment performance and implement corrective actions to resolve issues
  • Support statistical process control (SPC) and continuous improvement initiatives
  • Provide engineering support for design concepts and manufacturability
  • Ensure compliance with FDA, ISO, and GMP regulations
  • Collaborate with cross-functional teams including Quality, Operations, and R&D
*Other duties may be assigned.*


Requirements

  • Bachelor’s Degree in Engineering (Mechanical, Electrical, Chemical, or related)
  • 0–3 years of experience in manufacturing, engineering, or related roles
  • Bilingual (English & Spanish)
  • Experience in Computer System Validation (CSV)
  • Experience working in a regulated environment (Medical Devices or Pharmaceutical industry)
  • Basic knowledge of manufacturing processes and equipment
  • Strong organizational, communication, and technical writing skills

Preferred: 

  • Knowledge of Process Validation (IQ/OQ/PQ)
  • Experience with Statistical Tools (Minitab or equivalent)
  • Familiarity with MES systems (e.g., FactoryWorks)
  • Knowledge of risk management tools (FMEA)
*Willing to work 100% On-Site, weekend and other shifts when necessary.*





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