HOME None Manufacturing Engineer
  • EQVAL
  • Ponce, PR
  • Full-Time
  • 25 days ago
EQVAL VERIFIED EMPLOYER

Manufacturing Engineer.

None Full-Time

Manufacturing Engineer: our view in 3 lines...

  • The Role:This role is for a manufacturing engineer with experience in medical device or pharmaceutical industries.
  • The Person:The person will develop and execute validation activities, optimize manufacturing processes, troubleshoot equipment and processes, support NCR and complaint investigations, and ensure cGMP compliance.
  • Requirements:The ideal candidate has a Bachelor’s Degree in Engineering, at least three years of experience in Medical Device or Pharmaceutical industries, experience in validation documentation, investigations, Lean Manufacturing, Six Sigma tools, pFMEA, and is fully bilingual in English and Spanish.

About the role

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.

We are seeking Manufacturing Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes.

Responsibilities:

  • Develop and execute validation activities for equipment and process changes (IQ, OQ, PQ) and associated documentation.
  • Optimize manufacturing processes, ensuring efficient production layouts, material handling, and tool fabrication.
  • Troubleshoot and improve production equipment and processes to enhance operational efficiency and product quality.
  • Collaborate with cross-functional teams to support investigations (NCRs, Complaints) and implement corrective actions.
  • Ensure compliance with regulatory standards (cGMP) in all manufacturing processes and validation activities.

Minimum Requirements:

  • Bachelor’s Degree in Engineering.
  • Experience in developing and executing validation documentation (Validation Plans, URS, FRS, IQ, OQ, PQ).
  • Experience in investigations (NCRs, Complaints, CAPA), Lean Manufacturing, and Six Sigma tools.
  • Experience with pFMEA (analysis and development) and its application.
  • Fully bilingual (English and Spanish) spoken and written.
  • Good technical writing skills.

Benefits:

  • Health insurance (Medical, Dental, Vision, Pharmacy)
  • Life Insurance
  • Paid time off (PTO)
  • Holidays
  • Professional Growth (Courses and Certifications by EQVAL Academy)
  • Referral program
  • Productivity incentive

*This position will be full-time 100% on site in Dorado, Puerto Rico.

We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion, we would love to hear from you. Apply now!!

EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.

Published September 3, 2026
Location Ponce, PR
Category None  
Job Type Full-Time