Manufacturing Engineer

Medial Group; Barceloneta (PR); In loco; USD 70.000 - 95.000; Tempo pieno

Descrizione del lavoro

Medial Group seeks a motivated Manufacturing Engineer to support regulated medical device manufacturing. You will provide technical leadership, drive process improvements, and support validations with minimal supervision in Barceloneta, PR.

Responsibilities include leading project meetings, coordinating internal and external resources, and delivering status reports while ensuring compliance with quality requirements. Fluency in English and Spanish is valued for cross‑functional teamwork.

Competenze

• Minimum of 2 years engineering experience in the Medical Device or Pharmaceutical industry.
• Experience supporting manufacturing engineering projects in regulated environments.
• Ability to work independently with minimal supervision.

Mansioni

• Design, develop, communicate, and implement operational plans to complete engineering projects.
• Monitor project progress, timelines, budgets, and deliverables.
• Identify issues, implement corrective actions, and minimize delays.
• Develop engineering designs, work specs, schedules, budgets, and resource plans.
• Coordinate internal resources and external contractors for project execution.
• Collaborate with Engineering, Quality, Validation, Operations, Drafting, and Technical Services teams.
• Lead project meetings with status updates and technical reports.
• Prioritize tasks and coordinate resources to meet milestones.
• Conduct manufacturing studies, process evaluations, and line validations.
• Perform statistical analysis to support projects and improvements.
• Evaluate risks and mitigate to avoid delays.
• Generate, execute, review, and approve qualification and validation protocols/reports.
• Serve as technical liaison between cross-functional teams and Abbott sites.
• Support continuous improvement, cost reduction, and capital initiatives.
• Provide technical leadership for complex assignments requiring independent judgment.

Conoscenze

Manufacturing Engineering

Process Validation

Equipment Qualification

Statistical Analysis

Project Management

Process Improvement

Capital Projects

Cost Reduction Projects

Manufacturing Operations Support

Technical Report Writing

Cross‑Functional Collaboration

Formazione

Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Manufacturing Engineering, Industrial Engineering, Software Engineering, or related Engineering discipline

Descrizione del lavoro

Barceloneta, Puerto Rico | Posted on 07/10/2026

We are seeking a motivated and experienced Manufacturing Engineer to support manufacturing operations within a regulated Medical Device or Pharmaceutical environment. The selected candidate will provide technical leadership, execute engineering projects, drive process improvements, and support manufacturing validations while working with minimal supervision.

This role requires strong analytical and problem-solving skills, the ability to manage multiple engineering projects, and collaboration with cross‑functional teams to ensure manufacturing excellence and compliance with quality and regulatory requirements.

Responsibilities:

• Design, develop, communicate, and implement operational plans to successfully complete engineering projects.
• Monitor project progress, performance, timelines, budgets, and deliverables.
• Identify operational issues, implement corrective actions, and minimize project delays.
• Develop engineering designs, work specifications, project schedules, budgets, and resource plans.
• Coordinate internal resources and external contractors to support project execution.
• Collaborate with Engineering, Quality, Validation, Operations, Drafting, and Technical Services teams.
• Lead and coordinate project meetings while providing regular project status updates and technical reports.
• Prioritize tasks and coordinate project resources to meet established milestones.
• Conduct manufacturing studies, process evaluations, and line validations as required.
• Perform statistical analysis to support engineering projects and process improvements.
• Evaluate project risks, implement mitigation strategies, and proactively resolve issues before impacting project timelines.
• Generate, execute, review, and approve qualification and validation protocols and reports with minimal supervision.
• Serve as the technical liaison between cross‑functional teams and other Abbott manufacturing sites.
• Support continuous improvement, cost reduction, and capital improvement initiatives.
• Provide technical leadership for complex manufacturing engineering assignments requiring independent judgment and creative problem‑solving.
• Recommend innovative technical solutions when established procedures or precedents do not exist.

Requirements

Education

• Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Manufacturing Engineering, Industrial Engineering, Software Engineering, or related Engineering discipline.

Experience

• Minimum of 2 years of engineering experience in the Medical Device or Pharmaceutical industry.
• Experience supporting manufacturing engineering projects in regulated environments.
• Ability to work independently with minimal supervision.

Preferred Qualifications

• Experience with Equipment and Process Validations (IQ/OQ/PQ).
• Experience supporting Product Transfers.
• Experience managing Capital Projects.
• Experience leading Continuous Improvement initiatives.
• Experience with Cost Improvement Projects.
• Knowledge of statistical analysis and process optimization.
• Experience authoring and approving validation protocols and reports.

Technical Skills

• Manufacturing Engineering
• Process Validation (IQ/OQ/PQ)
• Equipment Qualification
• Statistical Analysis
• Project Management
• Process Improvement
• Capital Projects
• Cost Reduction Projects
• Manufacturing Operations Support
• Technical Report Writing
• Cross‑Functional Collaboration

Soft Skills

• Excellent analytical and problem‑solving skills.
• Strong project planning and organizational abilities.
• Ability to anticipate issues and develop proactive solutions.
• Excellent verbal and written communication skills.
• Ability to lead technical discussions across multidisciplinary teams.
• Self‑driven with the ability to work independently with minimal guidance.

Languages

• Fluent in English and Spanish (written and verbal).