Senior Manufacturing Engineer - Product Transfer Lead

Medial Group

Barceloneta (PR)

On-site

USD 90,000 - 120,000

Full time

14 days+
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Job summary

Medial Group is seeking a Senior Manufacturing Engineer to support a product transfer project within a regulated medical device manufacturing environment. The candidate will lead manufacturing engineering activities, validation efforts, and cross-functional collaboration to ensure successful transfers and compliant documentation.

The role requires independence, strong English communication, and proven problem-solving skills to optimize quality, efficiency, and reliability across processes and

Qualifications

  • Bachelor's Degree in Mechanical, Electrical, Software, Manufacturing, or related Engineering.
  • Minimum 5 years of Manufacturing Engineering experience.
  • Hands-on IQ, OQ, and PQ validations.
  • Ability to work independently with minimal supervision.
  • Strong written and conversational English communication skills.
  • Excellent analytical, troubleshooting, and problem-solving skills.
  • Strong organizational and project management abilities.

Responsibilities

  • Lead manufacturing engineering activities supporting product transfer projects.
  • Plan, execute, and support equipment and process validation activities, including OQ/PQ.
  • Generate technical reports, validation protocols, and engineering documentation.
  • Analyze manufacturing processes and recommend improvements to optimize quality, efficiency, and reliability.
  • Lead complex engineering assignments involving cross-functional teams.
  • Identify technical issues proactively and develop practical solutions with minimal supervision.
  • Collaborate with Quality, Operations, Validation, and other engineering disciplines to ensure project success.

Skills

IQ/OQ/PQ validations
Manufacturing engineering
Analytical skills
Project management

Education

Bachelor's degree in Engineering

Job description

Medial Group is seeking a Senior Manufacturing Engineer to support a product transfer project within a regulated medical device manufacturing environment. The candidate will lead manufacturing engineering activities, validation efforts, and cross-functional collaboration to ensure successful transfers and compliant documentation.

The role requires independence, strong English communication, and proven problem-solving skills to optimize quality, efficiency, and reliability across processes and

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