Sr. Spec, Restrictions Mgmt & Automation

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Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Affairs

Job Category:
Professional

All Job Posting Locations:
Diegem, Flemish Brabant, Belgium, New Cairo, Cairo, Egypt, Warsaw, Masovian, Poland

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 optimization   (e.g., workflow tools, data management platforms).

- Solid understanding of global regulatory frameworks   applicable to medical devices.

- Proven ability to analyze complex data,   identify   risks, and translate requirements into scalable solutions.

Preferred:

- Experience within medical devices   or other highly regulated healthcare industries.

- Hands ‑ on   experience with automation, RPA, or   low ‑ code / no ‑ code   platforms.

- Familiarity with SAP, regulatory information management (RIM), or master data systems.

- Experience supporting audits and inspections at a regional or global level.\

- Strong stakeholder management, communication, and documentation skills in a matrixed, international environment.

Other:

- Languages:   Fluency in English   required ;   additional   European languages preferred.

- Travel:   Limited; Up to ~10% international travel may be   required .

- Certifications:   Regulatory Affairs, Quality, Lean, Six Sigma, or   automation ‑ related   certifications preferred.

For more information on how we support the whole health of our employees throughout their wellness,   career   and life journey, please visit   www.careers.jnj.com .

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

#DePuySynthesCareers

Required Skills:

Preferred Skills:
Analytical Reasoning, Business Behavior, Business Writing, Communication, Confidentiality, Data Reporting, Detail-Oriented, Legal Support, Medicines and Device Development and Regulation, Problem Solving, Product Licensing, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments, Teamwork

The anticipated base pay range for this position is:
zł145,800.00 - zł234,600.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.