Manufacturing Engineer - Medical Devices (IQ/OQ/PQ) Onsite

EQVAL; Ponce (PR); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive compensation

Career growth opportunities

Job summary

EQVAL Group, Inc. is seeking a Manufacturing Engineer with at least three years of experience in the Medical Device or Pharmaceutical industries. This full-time role is 100% on site in Ponce, Puerto Rico. Responsibilities include executing validation protocols and optimizing manufacturing processes.

Qualified candidates will have a Bachelor’s Degree in Engineering, experience in validation documentation, and be fully bilingual in English and Spanish. Competitive compensation and benefits are offered.

Qualifications

• 3+ years of experience in Medical Device or Pharmaceutical industries.
• Experience in validation protocols (IQ, OQ, PQ) and regulatory compliance.
• Good technical writing skills, fully bilingual in English and Spanish.

Responsibilities

• Develop and execute validation activities for equipment and process changes.
• Optimize manufacturing processes for efficiency and quality.
• Troubleshoot and improve production equipment and processes.
• Support investigations and implement corrective actions.

Skills

Validation documentation development

Lean Manufacturing

Six Sigma tools

Technical writing

pFMEA application

Bilingual (English and Spanish)

Education

Bachelor’s Degree in Engineering

Job description

EQVAL Group, Inc. is seeking a Manufacturing Engineer with at least three years of experience in the Medical Device or Pharmaceutical industries. This full-time role is 100% on site in Ponce, Puerto Rico. Responsibilities include executing validation protocols and optimizing manufacturing processes.

Qualified candidates will have a Bachelor’s Degree in Engineering, experience in validation documentation, and be fully bilingual in English and Spanish. Competitive compensation and benefits are offered.