QRC Group, Inc

Process Engineer (Automation & Maintenance Support

QRC Group, Inc San Juan, Puerto Rico

Staffing and Recruiting · 51-200 employees

4 h ago
Mid (2-5 yrs) Contractor Puerto Rico
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About the role

The Process Engineer will support automated manufacturing operations by performing preventive maintenance, troubleshooting equipment issues, and optimizing process performance. They will collaborate with cross-functional teams to ensure compliance with safety, quality, and regulatory standards in a medical device manufacturing environment.

What they look for

Process Engineering Automation Preventive Maintenance Troubleshooting Root Cause Analysis Equipment Reliability Mechanical Engineering Electrical Engineering Manufacturing Engineering GMP Compliance Spare Parts Management Lean Manufacturing Continuous Improvement Packaging Systems Filling Systems Regulatory Compliance

Requirements

Candidates must hold a Bachelor's degree in Mechanical, Electrical, Industrial, or Manufacturing Engineering and be willing to work in North Carolina. Experience in supporting automated manufacturing or packaging equipment within a regulated industry is required.

Full description

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

We are seeking a Process Engineer to support automated manufacturing operations for a leading medical device manufacturer in North Carolina. This position will play a key role in maintaining equipment reliability, supporting production operations, troubleshooting process issues, and driving continuous improvement initiatives within a highly regulated manufacturing environment.

The selected candidate will provide technical and engineering support for automated filling, labeling, and formulation systems while collaborating with cross-functional teams to ensure safe, efficient, and compliant operations.

Essential Responsibilities

  •  Support and execute scheduled preventive maintenance activities on automated manufacturing equipment.
  • Troubleshoot equipment and process-related issues to minimize downtime and maintain production schedules.
  • Provide technical support during line operation, including equipment adjustments and process optimization.
  •  Assist with mechanical line changeovers and equipment setup activities.
  • Support spare parts management activities, including inventory monitoring and availability of critical components.
  • Investigate equipment failures and implement corrective and preventive actions.
  • Analyze equipment performance and identify opportunities for reliability and efficiency improvements.
  • Collaborate with Operations, Maintenance, Quality, and Engineering teams to resolve technical challenges.
  • Ensure all activities are conducted in compliance with safety, quality, and regulatory requirements.
  • Maintain accurate documentation of maintenance, troubleshooting, and improvement activities.

Equipment Experience Preferred

Experience supporting, maintaining, or troubleshooting the following equipment is desirable:

  • Shibuya Filling Systems
  • Optima Filling Systems
  • Groninger Filling Systems
  • Formulation Tank Farm Systems
  • Herma Labeling Equipment

Qualifications

Required Qualifications

  • Willing to work in North Carolina 
  • Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, Manufacturing Engineering, or related discipline.
  • Experience supporting automated manufacturing, packaging, filling, or production equipment.
  • Strong troubleshooting and root cause analysis skills.
  • Experience with preventive maintenance programs and equipment reliability practices.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Strong communication and problem-solving abilities.

Preferred Qualifications

  • Experience within the pharmaceutical, biotechnology, medical device, or life sciences industries.
  • Familiarity with GMP-regulated manufacturing environments.
  • Experience working with highly automated production systems.
  • Knowledge of spare parts management and inventory control.
  • Lean Manufacturing and/or Continuous Improvement experience.

Additional Information

All your information will be kept confidential according to EEO guidelines.