# Sr. Specialist, MDRIM & Document Mgmt. at Johnson & Johnson

Johnson & Johnson is hiring a Sr. Specialist, MDRIM & Document Mgmt. in Warsaw, Poland. It pays PLN 191k-PLN 308k a year and Level rates it Little AI ●○○○; you can [apply on Johnson & Johnson](https://jobsbylevel.com/go/66a5c76c-1e93-41a1-a9dc-955bb69586d5?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Warsaw, Masovian, Poland.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Warsaw, Masovian, Poland
- Salary: PLN 191k-PLN 308k
- Posted: October 5, 2026
- Apply: https://jobsbylevel.com/go/66a5c76c-1e93-41a1-a9dc-955bb69586d5?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=sr-specialist-mdrim-document-mgmt-at-johnson-johnson-2c2fdd

## Prepare for this job

The job page lists 4 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/sr-specialist-mdrim-document-mgmt-at-johnson-johnson-2c2fdd

## Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Regulatory Affairs Group Job Sub Function: Regulatory Affairs Job Category: Professional All Job Posting Locations: Warsaw, Masovian, Poland Job Description: DePuy Synthes is recruiting for a(n)Sr. Specialist, MDRIM & Document Mgmt., located in Warsaw, Poland. Job Overview The Sr. Specialist, MDRIM & Document Management is responsible for supporting the management, maintenance, and governance of regulatory information and controlled documentation within QARA International. This role serves as a subject matter expert for MDRIM and document management processes, ensuring regulatory data integrity, document compliance, and adherence to global quality and regulatory requirements. The Sr. Specialist partners closely with Regulatory Affairs, Quality, R&D, Manufacturing, and other cross-functional stakeholders to support regulatory submissions, product lifecycle activities, inspections, and continuous process improvements. This role contributes to operational excellence by ensuring accurate, compliant, and efficient management of regulatory information and documentation across international markets. Key Responsibilities Manage and maintain MDRIM and controlled document management activities in accordance with established quality systems, regulatory requirements, and internal procedures. Ensure the accuracy, completeness, and integrity of regulatory information, metadata, and controlled documents within applicable systems and repositories. Support the creation, review, processing, approval, and maintenance of quality and regulatory documentation throughout the product lifecycle. Collaborate with Regulatory Affairs, Quality, R&D, Manufacturing, and other stakeholders to ensure documentation and regulatory information requirements are met. Provide subject matter expertise on document management processes, data governance standards, workflows, and system requirements. Monitor document and data quality metrics, identify discrepancies, and drive timely resolution of documentation and regulatory information issues. Support regulatory submission and registration activities by ensuring required documentation and data are maintained and readily accessible. Contribute to inspection, audit, and compliance readiness efforts through effective document control and regulatory information management practices. Participate in continuous improvement initiatives to enhance MDRIM and document management processes, standardization, efficiency, and compliance. Assist with user training, process guidance, and procedural updates related to MDRIM and document management activities. Maintain documentation records, reports, and dashboards to support operational reviews and management decision-making. Apply DePuy Synthes quality principles and Johnson & Johnson Credo values in all activities. Qualifications Education Bachelor's degree required in Life Sciences, Engineering, Quality, Regulatory Affairs, Information Management, or a related discipline. Master's degree preferred. Experience and Skills Required 4-6 years of relevant experience in regulatory affairs, quality systems, document management, MDRIM, or related functions within a

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/sr-specialist-mdrim-document-mgmt-at-johnson-johnson-2c2fdd

Source: https://jobsbylevel.com/jobs/sr-specialist-mdrim-document-mgmt-at-johnson-johnson-2c2fdd

## Cite this page

Level. https://jobsbylevel.com/jobs/sr-specialist-mdrim-document-mgmt-at-johnson-johnson-2c2fdd.

Get job alerts: https://jobsbylevel.com/newsletter