Manufacturing Engineer: Validation & Method Transfer

Kelly Services; Arroyo (PR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Retirement savings plan

Paid holidays

Transit spending account

Job summary

Kelly® Engineering in Arroyo, Puerto Rico, seeks a Manufacturing Engineer to support validation and method transfer in a medical device environment. You will work with cross-functional teams to ensure methods are transferred and documented per quality requirements.

Responsibilities include planning/exec of validation activities, maintaining protocols and reports, and coordinating with Manufacturing, Quality, and Engineering while ensuring compliance and timely communication to stakeholders.

Qualifications

• Bachelor of Engineering in a related field, e.g., Mechanical, Industrial, Electrical, or Chemical.
• Experience in manufacturing, process validation, or method transfer; medical device experience preferred.
• Ability to prepare and review technical documentation with attention to detail.
• Ability to collaborate with cross-functional teams and manage project priorities.
• Fluency in English and Spanish, written and spoken, with professional context.

Responsibilities

• Support planning and execution of validation and method transfer activities.
• Prepare, review, and maintain technical documentation, protocols, and reports.
• Coordinate activities with Manufacturing, Quality, Engineering, and related teams.
• Analyze results, document findings, and follow up on corrective actions.
• Ensure activities comply with internal procedures and applicable requirements.
• Communicate project progress, risks, and results to stakeholders.

Skills

Process validation

Method transfer

Documentation

Cross-functional teamwork

Bilingual English/Spanish

Education

Bachelor’s degree in Engineering

Job description

Kelly® Engineering in Arroyo, Puerto Rico, seeks a Manufacturing Engineer to support validation and method transfer in a medical device environment. You will work with cross-functional teams to ensure methods are transferred and documented per quality requirements.

Responsibilities include planning/exec of validation activities, maintaining protocols and reports, and coordinating with Manufacturing, Quality, and Engineering while ensuring compliance and timely communication to stakeholders.