Senior Regulatory Affairs Specialist (Hybrid) - Stryker : Job Details

Senior Regulatory Affairs Specialist (Hybrid) page is loaded Senior Regulatory Affairs Specialist (Hybrid) Apply locations Redmond, Washington time type Full time posted on Posted 3 Days Ago job requisition id R546368 Work Flexibility: Hybrid We are currently seeking a Senior Regulatory Affairs Specialist to join our Medical Division to be based Hybrid Monday through Wednesday in Redmond, Washington.What you will doAs part of the Medical Regulatory Affairs team, you will work with the team to maintain medical devices on the market and ensure ongoing compliance.Support R&D, Marketing and Manufacturing teams with regulatory assessments of proposed changes or product transfersIdentify regulatory and market access requirements, including federal, state/provincial, reimbursement, and purchasing group considerationsDevelop and update regulatory strategiesin response to evolving regulations and product development needsEvaluate product classification and jurisdiction, and determine appropriate regulatory pathways and compliance requirements (local, national, international)Prepare and submit regulatory submissions(electronic and paper) in accordance with applicable guidelines and maintain communication with regulatory authorities throughout the review processProvide regulatory guidance throughout the product lifecycle, including development, planning, labeling, and claims, while maintaining current product registrationsAssess proposed pre-clinical, clinical, and manufacturing changesfor regulatory impact and recommend filing strategies or alternatives when submissions are not requiredBuild relationships and interface with cross-functional teams (Engineering, International RA, Manufacturing, Marketing, etc.) to ensure accurate, complete, and timely submission preparationWhat you needRequiredBachelor's degree in an Engineering, Science, or equivalent fieldMinimum of 2 years of experience in an FDA or highly regulated industryMinimum of 1 year in a Regulatory Affairs rolePreferredRAC certification or Advanced Degree (Masters in Regulatory Affairs)Previous experience with Class II/III medical devicesExperience authoring regulatory submissions for product approvalExperience interacting with regulatory agencies$88,000.00 - $142,300.00 salary plus bonus eligible + benefits.Individual pay is based on skills, experience, and other relevant factors.Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.#J-18808-Ljbffr