9 Ofertas de Abbott en Costa Rica

We are hiring a Project Manager in the Medical Devices industry

We are looking for an experienced professional to lead engineering projects that drive innovation, ensure compliance, and strengthen operational excellence across R&D, manufacturing, quality, and supply chain.

• Lead cross-functional projects that support manufacturing processes and continuous improvement.
• Manage project schedules, budgets, and resources, ensuring timely delivery of milestones.
• Ensure compliance with FDA, ISO 13485, EU MDR, and other applicable regulatory standards.
• Collaborate with regulatory, quality, and operations teams to achieve aligned project outcomes.
• Mentor junior engineers, provide technical guidance, and present progress updates to leadership.

If you are a results-driven leader with strong organizational and communication skills, we encourage you to apply.

• 5+ years of experience in Project or Program Management within the Medical Devices industry.
• Fluency in English and Spanish (minimum B2).
• Strong background in risk management, process validation, and regulatory documentation.
• Proven ability in conflict resolution and problem solving.
• Preferred: experience in process or product transfers.
• Bonus: PMP certification and/or MBA.

We are hiring a Senior Manufacturing Engineer in the Medical Devices industry

We are looking for a highly skilled professional to drive the development, implementation, and continuous improvement of manufacturing processes. This role plays a critical part in ensuring compliance with product specifications, quality standards, and FDA regulations.

Key Responsibilities

• Perform installation and validation activities for production lines, including equipment, process, product, and test method validations, in compliance with regulations.
• Design and implement manufacturing processes, procedures, and production layouts for assemblies, equipment, and material handling.
• Support product improvements in areas such as risk management, test method validation, process validation, process control, supplier qualification, complaint investigations, CAPA, and process improvement.
• Execute and manage documentation in PLM systems (e.g., update DHRs, BOMs, work instructions, and create part numbers).
• Investigate and resolve production issues using structured problem-solving methods.
• Lead or support cross-functional manufacturing projects and initiatives.
• Provide guidance to engineering teams on design concepts and specifications to optimize manufacturing efficiency.
• Ensure compliance of processes and procedures with all applicable regulatory requirements.

We are seeking a results-driven engineer with a strong technical background and proven ability to lead complex manufacturing initiatives. If this opportunity aligns with your expertise, we encourage you to apply.

Requirements
Qualifications

• 5+ years of experience as a Manufacturing Engineer in the
  Medical Devices
  industry.
• Fluency in English and Spanish (minimum B2).
• Experience leading validation plans for medical products and processes.
• Hands-on experience in product and process transfers.
• Strong background in root cause analysis and problem-solving methodologies.
• Project Management experience is considered a plus.
• Strong documentation and communication skills.

We are hiring a Senior Manufacturing Engineer in the Medical Devices industry

We are looking for a highly skilled professional to drive the development, implementation, and continuous improvement of manufacturing processes. This role plays a critical part in ensuring compliance with product specifications, quality standards, and FDA regulations.

• Perform installation and validation activities for production lines, including equipment, process, product, and test method validations, in compliance with regulations.
• Design and implement manufacturing processes, procedures, and production layouts for assemblies, equipment, and material handling.
• Support product improvements in areas such as risk management, test method validation, process validation, process control, supplier qualification, complaint investigations, CAPA, and process improvement.
• Execute and manage documentation in PLM systems (e.g., update DHRs, BOMs, work instructions, and create part numbers).
• Investigate and resolve production issues using structured problem-solving methods.
• Lead or support cross-functional manufacturing projects and initiatives.
• Provide guidance to engineering teams on design concepts and specifications to optimize manufacturing efficiency.
• Ensure compliance of processes and procedures with all applicable regulatory requirements.

We are seeking a results-driven engineer with a strong technical background and proven ability to lead complex manufacturing initiatives. If this opportunity aligns with your expertise, we encourage you to apply.

• 5+ years of experience as a Manufacturing Engineer in the Medical Devices industry.
• Fluency in English and Spanish (minimum B2).
• Experience leading validation plans for medical products and processes.
• Hands-on experience in product and process transfers.
• Strong background in root cause analysis and problem-solving methodologies.
• Project Management experience is considered a plus.
• Strong documentation and communication skills.