Job Description

Empowering careers at ARJO

At Arjo, we know what moves us. We go above and beyond for people facing mobility challenges. We take every opportunity to work and grow as one team and take pride in sharing our knowledge and experience. Does that sound like something that moves you too?

This could be your opportunity to begin a challenging and rewarding career in a healthcare company that empowers movement for people with mobility challenges.

The Documentation Laead is responsible for managing engineering documentation projects related to product lifecycle maintenance, quality improvement, cost reduction, and regulatory compliance, ensuring proper coordination, accurate documentation, and timely execution of activities while collaborating with cross-functional teams and supporting departmental processes and systems.

Key Duties and Responsibilities:
• Manage and coordinate documentation-related engineering projects.

• Manage ECN workflows
• Ensure accurate, complete, and compliant project documentation.
• Plan and monitor timelines to meet documentation deliverables.

• Collaborate with cross-functional teams to support project execution.
• Create and maintain product and packaging labeling content.
• Support onboarding and use of documentation systems and tools.

Knowledge/ Skills / Experiencie

• Administrative or technical degree (Industrial engineer, or bachelor in business administration) combined with 3–5 years of experience in documentation, project coordination, or a related role.
• Experience managing documentation within engineering or product-related projects (e.g., maintenance, quality improvement, regulatory compliance). Experience in the regulated industry is a plus.
• Strong project planning and organizational skills, with the ability to manage timelines and priorities.

• Proficiency in Microsoft Office tools for document creation, formatting, and management.
• Ability to learn and effectively use enterprise systems such as ERP, PLM/PDM, and labeling software.
• Experience working with product and packaging labeling content and documentation processes.

• Understanding of documentation requirements in regulated environments (e.g., medical device, automotive, aerospace) is an asset.
• Strong attention to detail to ensure accuracy, consistency, and compliance of documentation.
• Good communication and collaboration skills to work effectively across departments.

• Proficiency in English (written and verbal) in a professional environment.
• Professional certifications in quality (e.g., ASQ CQIA, CSSGB) are preferred but not mandatory.

• This job wll be based at Bajos de Haina, San Cristóbal, República Dominicana.

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About Arjo

At Arjo, we believe that empowering movement within healthcare environments is essential to quality care. Our products and solutions are designed to promote a safe and dignified experience through patient handling, medical beds, personal hygiene, disinfection, diagnostics, and the prevention of pressure injuries and venous thromboembolism. With over 6500 people worldwide and 65 years caring for patients and healthcare professionals, we are committed to driving healthier outcomes for people facing mobility challenges.

For more information about Arjo visit www.arjo.com