Manufacturing Engineer

Kelly; Arroyo (PR); On-site; USD 55,000 - 83,000; Full time

Job summary

Kelly® Engineering in Arroyo, Puerto Rico seeks a Manufacturing Engineer for a contract role focused on validation and method transfer in a medical device environment. You will work with cross-functional teams to ensure processes are transferred and documented to meet quality requirements.

The ideal candidate holds an engineering degree and has experience in manufacturing, process validation, or method transfer, with strong documentation and bilingual Spanish/English skills.

Qualifications

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

Responsibilities

• Support the 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 are performed in accordance with internal procedures and requirements.
• Communicate project progress, risks, and results to stakeholders.

Job description

Kelly® Engineering is seeking Manufacturing Engineer – Validation and Method transfer for contract position at manufacturing client in Arroyo, Puerto Rico. If you’re passionate about bringing the latest professional discoveries to life and are ready to take the next step in your career.

Manufacturing Engineer — Validation and Method Transfer Project

We are seeking a Manufacturing Engineer to support a validation and method transfer project in a medical device manufacturing environment. The selected candidate will work with cross‑functional teams to ensure processes and methods are transferred and documented in accordance with applicable quality requirements and procedures.

Responsibilities

• Support the 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 other related teams.
• Analyze results, document findings, and follow up on corrective actions and outstanding items.
• Ensure activities are performed in accordance with internal procedures and applicable requirements.
• Communicate project progress, risks, and results to stakeholders.

Qualifications

• Bachelor’s degree in Engineering, preferably Mechanical, Industrial, Electrical, Chemical, or a related discipline.
• Previous experience in manufacturing, process validation, or method transfer; medical device experience is preferred.
• Ability to prepare and review technical documentation with strong attention to detail.
• Ability to collaborate with cross‑functional teams and manage project priorities.
• Fluency in spoken and written Spanish and English, with previous experience using English in a professional environment.