Engineer - 35737- Juncos, PR - 1st & 2nd shift availability

Integrated Services for Productivity & Validation, Inc; Juncos (PR); On-site; USD 65,000 - 85,000; Full time

Job summary

Integrated Services For Productivity & Validation, Inc. seeks an Engineer for the Juncos, PR area to support GMP-compliant manufacturing activities. The role emphasizes accurate technical reporting, CAPA handling, and cross-functional problem solving in a production setting.

The ideal candidate holds an engineering degree with 2 years of experience and is fluent in Spanish and English, ready to work first or second shift and extend hours as needed to meet project deadlines.

Qualifications

• Experience in GMP-regulated environments (pharma, medical devices or biotech).
• Proficiency in technical report writing.
• Bilingual in Spanish and English (verbal and written).
• Familiarity with packaging equipment, process characterization, validation, monitoring and optimization.
• Strong problem-solving skills with root-cause investigations.
• CAPA (Corrective and Preventive Actions) management experience.
• Proficiency in statistics and DOE methodologies.
• Apply engineering principles to solve production issues.
• Willingness to support non-standard shifts (nights, weekends, holidays).

Skills

GMP experience

Technical report writing

Bilingual Spanish/English

Packaging equipment familiarity

CAPA management

Statistics & DOE

Root cause investigations

Production engineering

Engineering principles application

Education

Engineering degree (Bachelor's or Master's)

Job description

Integrated Services For Productivity & Validation, Inc | Contract

Engineer - 35737- Juncos, PR - 1st & 2nd shift availability

Juncos, Puerto Rico | Posted on 09/17/2026

We provide the industry with a platform of solutions designed to their actual needs. We share and implement leading edge technology and methods that exceed customer expectation and deliver a one-stop provider of services focus on the well-being of the company and the employees.

Job Description

Experience working in a GMP-regulated environment within the pharmaceutical, medical device, or biotechnology industry

Proficiency in technical report writing

Effective communication skills in both Spanish and English (verbal and written)

Familiarity with packaging equipment, process characterization, validation, monitoring, and optimization techniques

Strong problem-solving skills and experience conducting root cause investigations

Expertise in identifying and managing Corrective and Preventive Actions (CAPAs)

Proficiency in statistical analysis and Design of Experiments (DOE) methodologies

Ability to apply engineering principles to solve technical issues in a production environment

Availability to support non-standard shifts, including extended hours, nights, weekends, and holidays

Requirements

Master's degree OR Bachelor's degree in Engineering & 2 years of Engineering experience