Sr. Spec, Restrictions Mgmt & Automation

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: Cairo, Egypt Job Description: DePuy Synthes is recruiting for a(n) Sr. Spec, Restrictions Mgmt & Automation , this Hybrid position will be in Warsaw, Poland. Alternate Hybrid locations may be considered at New Cairo, Egypt and Diegem, Belgium. Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): Warsaw, Poland - Requisition Number: 097945 New Cairo, Egypt - Requisition Number: 100001 Diegem, Belgium - Requisition Number: 097945 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission. Job Overview This role sits within QARA International and plays a critical part in enabling compliant, efficient global product availability. The Sr. Specialist, Restrictions Management & Automation leads the execution and continuous improvement of restriction controls, digital workflows, and automation solutions that support regulatory compliance, market access, and supply continuity across international markets. The role partners closely with Regulatory Affairs, Quality, Supply Chain, IT/Digital, and regional teams to reduce manual effort, increase transparency, and strengthen governance through scalable, automated solutions. Key Responsibilities Own and manage global and regional restrictions management processes, ensuring accurate interpretation, documentation, and execution of regulatory and quality ‑ driven restrictions. Design, implement, and optimize automation and digital solutions (e.g., workflows, dashboards, rule ‑ based controls) to improve efficiency, accuracy, and compliance. Partner with QARA, Supply Chain, and Commercial stakeholders to assess restriction impacts on product availability and market access, and support risk ‑ based decision making. Lead data governance activities related to restrictions, including master data quality, documentation standards, and audit readiness. Monitor regulatory and quality changes globally and assess implications for existing restriction logic and automated controls. Drive continuous improvement initiatives using structured problem ‑ solving and process optimization methodologies. Provide subject matter expertise and training to regional teams on restrictions management tools and processes. Support internal and external audits and inspections by preparing documentation and responding to inquiries related to restrictions and automation controls. Qualifications Education: Bachelor’s degree required (e.g., Life Sciences, Engineering, Information Systems, Regulatory Affairs, or related field). Advanced degree or relevant postgraduate certification preferred. Experience and Skills: Required: Typically 6–8 years of professional experience in Quality, Regulatory Affairs, Compliance, Supply Chain, or related regulated ‑ industry environment, consistent with a senior specialist level. Demonstrated experience managing regulatory or quality ‑ driven restrictions across multiple markets. Strong experience with process automation, digital tools, or systems opt