PpbJoin Our Team at HuFriedyGroup – Innovating Excellence in Dental Instrument Manufacturing /b /ppHuFriedyGroup is a leading manufacturer of dental instruments and infection prevention products. Our 10,000-plus products, hand-crafted by highly skilled artisans, are known for their precision, performance, longevity, reliability, and quality. To help dental professionals be The Best in Practice, HuFriedyGroup provides a unique combination of world class products, value-added services, clinical education, and dental community platforms that bresult /b in superior clinician performance and enhanced safety for dental professionals and their patients. Working at HuFriedyGroup is so much more than a job, as every employee has a part in driving and supporting the organization’s inspirational vision to be a global force in advancing dental performance through Best-In-Practice dentistry that improves lives around the world. /ph3Job Purpose /h3pThe Regulatory Affairs Specialist is responsible for regulatory affairs and compliance activities for HuFriedy Group global markets. Execute regulatory affairs tasks to support achievement of business objectives. Determine regulatory pathway and requirements for new and revised products. Determine and define regulatory requirements for stakeholders throughout the company. Plan, develop, prepare and execute regulatory submissions to regulatory agencies worldwide. Facilitate achievement of business objectives while ensuring compliant operation within the flexibility of the regulations. Operate in matrix organization and collaborate with HuFriedy Group corporate regulatory affairs team to achieve corporate and enterprise business objectives. /ppFacilitate HuFriedy Group organizational cohesiveness and compliance consistency and integration of businesses. Responsible for both pre-market regulatory and product development activities, international submission and post-market regulatory activities. Facilitate and manage in close collaboration with quality and compliance personnel inspections and audits by applicable regulatory agencies including FDA, MDD, MDR, and EU Notified Bodies. /ph3Essential Duties and Responsibilities /h3ulliExecute regulatory affairs and compliance activities for HuFriedy Group product lines in worldwide markets. /liliEnsure company products, manufacturing operations, and analytical laboratory practices comply with applicable regulatory and standard requirements including US-FDA cGMP, EU Medical Device Directives and Regulation, and ISO 13485 requirements. /liliPlan, develop, prepare and execute regulatory submissions to regulatory agencies worldwide. Collaborate closely with HuFriedy Group corporate regulatory affairs team to achieve corporate and enterprise business objectives. /liliParticipation in ensuring design and process validations, and test methods analysis comply with applicable regulations and industry standards, such as US-FDA 21 cfr Part 820, EU MDR 2017/745 and ISO 13485. /liliReview and determine regulatory implications of product, labeling, and/or other documentation or design changes. /liliPlan, develop and supervise product packaging/labeling creation and maintenance in collaboration with Marketing/Sales/Purchasing departments and in compliance with the identified applicable regulatory requirements. /liliParticipate on project teams to provided regulatory leadership and input. Provide recommendations for how to overcome regulatory barriers and resolve any disputes within teams as to the need and importance of regulatory requirements. /liliCollaborate with management in establishing departmental goals, strategies, and procedures in support of business objectives /liliParticipation in pre and post market regulatory and product development activities, international product registrations. /liliFacilitate, manage, and collaborate with quality and compliance personnel during establishment inspections and audits by Notified Bodies and Competent Authorities; /liliMust be able to travel up to 10% locally and internationally. /li /ulh3Knowledge, Skills and Ability /h3ulliDegree in pharmaceutical chemistry or similar science or related technical discipline. /lili3-5 years of regulatory experience within US-FDA – European Medical Device regulated industry. /liliExperience in planning and preparing US-FDA 510K, MDD/MDR Technical Files, and international submissions is required. /liliGood English language skills. /liliDemonstrated history of successful regulatory affairs and compliance outcomes to support business objectives. /liliKnowledge of US-FDA Medical Device regulations, EU Medical Device Regulation, and ISO 13485. Familiarity with sterile packaged device requirements is a plus. /liliStrong written and verbal communication skills, especially when dealing with governmental agencies. /liliAbility to explain and resolve differences between and within regulations. /liliDemonstrated experience in developmental and execution of regulatory strategy. /li /ul /p #J-18808-Ljbffr