Senior Regulatory Compliance Specialist

**Job Function**:Legal & Compliance**Job Sub Function**:Enterprise Compliance**Job Category**:Professional**All Job Posting Locations**:Ciudad Juarez, Chihuahua, Mexico**About MedTech**Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.**About Cardiovascular**Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.Are you passionate about improving and expanding the possibilities of Cardiovascular?Ready to join a team that's reimagining how we heal?Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.**We are searching for the best talent for**Senior Regulatory Compliance Specialist** to be in Cd.Juarez, in plant Salvarcar.****Purpose**:Conducts audits— planned and unplanned — to verify compliance with government regulations and applicable standards, in addition to company policies and procedures.Give guidance or advice to the organization as it relates to compliance, when required.**You will be responsible for**:Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:- Ensures that Quality System Audits comply with the requirements of QSR/GMP and ISO Standards- Conducts internal audits of the Quality System for the purpose of verifying compliance with government regulations and applicable standards, in addition to company policies and procedures.Conducts good laboratory practice (GLP) audits as required.- Gives guidance or advice as it relates to compliance with applicable standards and regulations.- Performs re-audits to deficient aspects and to implement corrective and preventive actions as necessary and required.- Assigns classifications to internal audit observations and documents audit results in written reports that can be distributed and reviewed by appropriate management.- Monitors the effectiveness of corrective actions documented in observation responses.- He/She can be the lead auditor of a team of auditors, technical experts, auditors-in-training, and/or volunteer auditors.- Reviews ownership of responses to audit observations, also acts as an advisor to other areas that are not being audited by him/her, giving advice on audit observation responses.- Maintains audit report files, re-audit files and responses to audits carried out.- Accompanies external auditors, representatives of government agencies or those required by management during the execution of an applicable audit.- Conducts audits at other J&J sites when required by management.- Prepares, reviews and ensures compliance related metrics; communicates them to site management and Franchise.Prepares information for Management review meetings and/or other forums as required (QSMR, DRB, QPR, Quality Metrics).- Keeps abreast of government regulations and applicable standards changes through publications, participation in seminars or through collaboration with organizations.- Participates in the formulation of Regulatory Policies and Procedures in compliance with applicable local, state and federal standards and regulations through the development of Franchise Documents.- Responsible for communicating business related issues or opportunities to next management level- Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.- For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures- Performs other duties assigned as needed**Qualifications / Requirements**:- BS in science, engineering, or business.- MBA or Master's in Science, preferably.- Minimum 3 years of experience in Quality, Regulatory Compliance, or related activities and demonstrated performance.- Experience in Medical Devices field or in Pharmaceuticals (preferably)- Lead Auditor Certification by an accredited organization preferred.- Effective communication skills - oral and written - (English and Spanish).- Analytical skills to interpret scientific and technical publications and legal documents.- Ability to select, manage and lead a team during an audit.- Ability to respond to questions or complaints from clients, regulatory agencies or members of the business community.- Skills to present information effectiv