Manufacturing Engineer (2nd Shift)
Quick Summary
Support the creation, execution, and maintenance of qualification and validation activities related to manufacturing processes and systems.
(The day-to-day on the job)Key Responsibilities include, but are not limited to, the following: Support the creation, execution, and maintenance of qualification and validation
For Manufacturing services in the Engineering area.
WHAT MAKES YOU A FIT: .png)
The Technical Part:
- Bachelor's Degree in Mechanical, Electrical, Industrial, Manufacturing, or Biomedical Engineering, or a related technical field, and 2–3 + years of experience manufacturing environment, including the generation and execution of validation protocols for manufacturing equipment.
- Bilingual (English & Spanish).
- Shift: 2nd shift (12:00pm-9:00pm) and according to business needs.
- Experience in:
- Generation and execution of validation protocols for manufacturing equipment.
- Qualification, validation, and lifecycle management of manufacturing systems and equipment.
- GMP documentation development, including protocols, reports, risk assessments, deviations, and CAPAs.
- Manufacturing process support, troubleshooting, compliance, and continuous improvement initiatives.
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
Key Responsibilities include, but are not limited to, the following:
- Support the creation, execution, and maintenance of qualification and validation activities related to manufacturing processes and systems.
- Generate and maintain manufacturing and system documentation required to support process changes, equipment implementation, and compliance requirements.
- Actively support the execution of validation and qualification protocols and generate supporting reports.
- Provide ongoing support for daily manufacturing operations and process performance monitoring.
- Support activities related to quality system processes and manufacturing compliance requirements.
- Monitor manufacturing metrics and assist in identifying opportunities for improvement.
- Coordinate qualification, validation, and protocol execution activities across Manufacturing, Quality, and Engineering teams.
- Prepare, review, and maintain qualification protocols, validation reports, risk assessments, and other compliance-related documentation.
- Support deviation investigations, CAPA activities, and data integrity initiatives to ensure regulatory compliance.
- Monitor manufacturing yields, process performance trends, and key performance indicators to identify and support continuous improvement opportunities.
WHO WE ARE:
We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!
Are you the next piece?
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Location & Eligibility
Listing Details
- Posted
- October 7, 2026
- First seen
- October 7, 2026
- Last seen
- October 7, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 56%
- Scored at
- October 7, 2026
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