Work Flexibility: Remote or Hybrid or Onsite Join our team as a Senior Regulatory Affairs Specialist! This person will for a key part of our Regulatory Affairs function, servicing the GSA region and will be exposed to a broad range of Stryker products. Do you have a strong understanding of regulatory framewrok? Are you looking for a challenging role that will push your knowledge in this sector? Apply today! Key Areas of Responsibility: Executes post-market surveillance activities with focus on Complaint Handling, Product Field Actions (PFA/FSCA), Commercial Holds and related Post Market activities (PMS) activities. Coordinates the intake, processing, follow-up and closure of product complaints and ensures complete and timely documentation in applicable quality systems. Coordinates local execution of Product Field Actions, recalls and Commercial Holds, including assessment of local impact, containment, customer communication, reconciliation, product return/destruction and closure activities. Reviews product scope, distribution and inventory information and coordinates required actions with relevant local, regional and divisional stakeholders. Acts as an operational interface between RAQA, Central/Regional PMS, Legal Manufacturers/Divisions, Customer Service, Sales, Supply Chain, Distribution/Warehouse and other relevant stakeholders. Proactively coordinates and follows up on outstanding actions, clarifies responsibilities, and escalates delays, gaps or compliance risks as appropriate. Supports communication with Competent Authorities and other external stakeholders on post-market surveillance matters. Maintains systems to track, manage and report product complaints, field actions, Commercial Holds and other product-associated events. Monitors assigned cases, timelines and execution status and ensures activities are completed in line with applicable procedures and defined timelines. Supports complaint trending Monitors the post-market environment, including applicable regulations, guidance and other relevant information. Supports the development, implementation and continuous improvement of PMS procedures, SOPs, work instructions and training materials. Provides PMS process guidance and operational support to internal stakeholders and promotes awareness and understanding of Complaint Handling and PFA/HOLD processes. Supports preparation for regulatory inspections, internal and external audits and other PMS-related assessments. Prepares and monitors RAQA/PMS metrics and KPIs and supports identification of trends, backlogs and opportunities for continuous improvement Identifies opportunities to improve the effectiveness and efficiency of PMS processes and supports implementation of improvement activities across RAQA. Education / Work Experience: BSc in Engineering, Science, Regulatory Affairs, Quality Management, Business Administration or related degree; equivalent relevant professional experience may be considered. 2+ years’ relevant experience in Regulatory Affairs, Quality Assurance, Post-Market Surveillance, Complaint Handling or another regulated medical-device environment. Experience working in a cross-functional and international matrix organization preferred. Knowledge / Competencies: Good understanding of Post-Market Surveillance, Complaint Handling, Vigilance, Product Field Actions/FSCA, recalls and Commercial Holds within the medical-device environment. Strong project, time and priority management skills, with the ability to independently manage multiple parallel PMS activities and deadlines. Resilient and comfortable working in an environment with changing priorities, urgent activities and competing deadlines. Strong problem-solving skills and ability to exercise sound judgement when dealing with incomplete or changing information. Demonstrates ownership and drives assigned activities from initiation through follow-up and completion with minimal supervision. Strong coordination and stakeholder-management skills with the ability to work effectively across functions, countries, divisions and organizational levels. Clearly and confidently communicates regulatory and quality requirements to internal and external stakeholders. Proactively follows up on outstanding information and actions and appropriately escalates delays, unclear responsibilities or compliance risks. Ability to create structure and direction in complex situations involving multiple stakeholders and changing priorities. Ability to review and interpret product, complaint, distribution and quality information and translate requirements into practical execution activities. Communicates and advises other departments and business units on post-market surveillance requirements and processes. Engages with Competent Authorities and other key stakeholders on routine and more complex matters with appropriate support. Supports preparation of briefings, regulatory correspondence and other PMS documentation. High attention to detail, process consciousness and strong documentation skills. Ability to identify process inefficiencies and actively contribute to continuous improvement and standardization. Strong interpersonal skills and ability to build effective working relationships within a complex matrix organization. Strong IT skills, including Microsoft Office; experience with quality systems such as TrackWise and reporting tools is advantageous. Fluent in German and English; additional languages are beneficial. Germany Pay Ranges: Freiburg/Stetten 35Std: €4.211 - €7.049 EUR Monthly Schonkirchen/Kiel 35Std: €4.562 - €7.637 EUR Monthly Freiburg/Stetten 39Std: €4.692 - €7.855 EUR Monthly Tuttlingen 40Std: €4.813 - €8.056 EUR Monthly Berlin/Duisburg/Waghäusel/field-based 40Std: €63.000 - €104.900 EUR Annual At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package. If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process. Travel Percentage: 10% Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

Senior Regulatory Affairs Specialist.

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