Manufacturing Engineer (2nd Shift)

fitspr

Dorado (PR)

On-site

USD 65,000 - 90,000

Full time

5 days ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

FITS is seeking a qualified engineer to support validation and qualification of manufacturing equipment and processes on 2nd shift (12:00pm-9:00pm) in Puerto Rico. The role requires a Bachelor's degree in engineering and 2–3+ years in a manufacturing setting.

Bilingual in English and Spanish is required. Responsibilities include GMP documentation, protocol execution, and collaboration with Quality and Engineering teams to drive continuous improvement.

Qualifications

  • Bachelor's Degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering or related field.
  • 2+ years in manufacturing with validation protocol execution.
  • Bilingual (English & Spanish).

Responsibilities

  • Support creation, execution, and maintenance of qualification and validation activities for manufacturing processes and systems.
  • Generate and maintain manufacturing and system documentation for process changes and equipment implementation.
  • Assist in validation/qualification protocols and associated reports.
  • Provide ongoing support for daily manufacturing operations and process performance monitoring.
  • Support quality system processes and manufacturing compliance requirements.
  • Monitor manufacturing metrics and identify opportunities for improvement.
  • Coordinate qualification, validation, and protocol execution across Manufacturing, Quality and Engineering teams.
  • Prepare and maintain qualification protocols, validation reports, risk assessments, and other compliance docs.

Skills

Bilingual English/Spanish
Validation protocols
Quality system understanding

Education

Bachelor's in Engineering or related field

Job description

WHAT MAKES YOU A FIT:
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 companydifferent 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 industryclients with top-notch quality talent.We're FITS!

Are you the next piece?

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Manufacturing Engineer (2nd Shift)
Manufacturing Engineer (2nd Shift)

FITS LLC • Dorado (PR), Northern (KY)

On-site
USD 60,000 - 80,000
Manufacturing Engineer - 02
Manufacturing Engineer - 02

FITS LLC • Juncos (PR)

On-site
USD 65,000 - 90,000
Manufacturing Engineer
Manufacturing Engineer

FITS, LLC • Juncos (PR)

On-site
USD 70,000 - 90,000
Manufacturing Engineer
Manufacturing Engineer

FITS LLC • Juncos (PR)

On-site
USD 65,000 - 90,000
Manufacturing Engineer - 02
Manufacturing Engineer - 02

FITS, LLC • Juncos (PR)

On-site
USD 60,000 - 90,000
Maintenance Engineer - 04
Maintenance Engineer - 04

FITS LLC • Juncos (PR)

On-site
USD 65,000 - 86,000
Manufacturing Technician II
Manufacturing Technician II

FITS LLC • Juncos (PR)

On-site
USD 40,000 - 60,000
Process Engineer II
Process Engineer II

FITS LLC • Humacao (PR)

On-site
USD 60,000 - 80,000
Quality Engineer I
Quality Engineer I

FITS, LLC • Humacao (PR)

On-site
USD 65,000 - 90,000
Sr. Associate Manufacturing Systems
Sr. Associate Manufacturing Systems

FITS LLC • Juncos (PR)

On-site
USD 55,000 - 85,000