PQV Combination Product Analyst IV

pAt Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. /p pAs guided by Our Credo, Johnson Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. /p pbJob Function: /b Quality /p pbJob Sub Function: /b Quality Assurance /p pbJob Category: /b Professional /p pbAll Job Posting Locations: /b Beerse, Antwerp, Belgium, Little Island, Cork, Ireland, Schaffhausen, Switzerland /p pThe PQV Combination Product Analyst 4 will be responsible for handling high-volume E2E product quality complaint activities and adverse events, including performing Medical Device Reporting (MDR) assessments. Additionally, the Analyst IV Combination Products will provide instruction and feedback to the group as needed and ensure completeness and consistency of complaint and MDR documentation. The position manages and collaborates with business partners and stakeholders (Out Sourced Management Team, Clinical, PV, IT, Local Operating Companies, ESIQ, Call Centers, Brand Protection, External Manufacturing Sites, Internal/External Manufacturing Sites, QA, Business Quality, Medical Safety and RD) to deliver effective change management, drive process improvements and identify opportunities to improve the accuracy, efficiency and timeliness of the complaint and MDR processes. /p pThis may include risk assessing the impact of proposed changes to the complaint handling/MDR process within and across functional/regional areas and supporting the global change management effectively. The Analyst IV must have the ability to lead projects and communicate effectively with all levels of management as part of stakeholder engagement and change management roll out. /p h3Position duties responsibilities: /h3 ul liPerform high-volume end-to-end complaint handling activities, including, but not limited to: Intake, triage and review of the event reported, determination of MDR reportability, recovery of field samples for evaluation, determination of Priority/Non-Priority, and QP notification to LOC. Additional activities include due diligence to be performed with the complainant/intake centers/LOC, trend analysis, defect coding, risk criticality assessment, ensuring accurate/holistic investigation, and review and closure. /li liEvaluate complaints to determine if the QTL’s or ULC’s have been exceeded, assess the level of investigation required, and assign to the applicable site for investigation. /li liGovernance and oversight for daily thru put of complaints and MDR decisions to ensure prioritization and KPI are met. /li liPerform MDR evaluations and document written justification to support reportable and non-reportable regulatory decisions. /li liMonitor complaints for new malfunction events that may require inclusion in the malfunction description list (MDL). /li liServe as a PQV point person for post market and complaint handling regulatory/MDR questions and inquiries; provides guidance and direction to subordinate Analyst roles and other PQV functions. /li liEvaluate information from a technical perspective to ensure appropriate analysis and investigations/ MDR’s are accurately assessed for risk prioritization and performed per procedures, standards, and regulations. /li liBack-up Product Quality Vigilance Investigation Support (PQVIS) personnel to support increased volume of complaints. /li liStrong collaboration with Global Medical Safety, manufacturing sites, and LOC/BQ for effective complaint handling/MDR assessments and adverse events with potential product quality issues. /li liUse technical and product knowledge to provide accurate feedback for escalation/awareness of issues and for current product enhancements/future product development, if applicable. /li liEnsure that uniform and timely management of complaint records and regulatory reporting occurs per procedures, standards, and regulations. /li liCompile and analyze data, metrics, and trends associated with the complaint handling processes. /li liSupport internal and external audits and inspections; ability to communicate regulatory and process positions as an SME during regulatory inspections and provide follow-up support as required. /li liMay interact with regulatory authorities, other JJ operating companies, and JJ global councils to interpret and influence emerging quality systems regulatory trends. /li liProvide product workflow leadership to PQV peers to ensure consistent and fully understood End-to-End complaint management process. /li liOversee the PQC complaint monitoring process and analyze the outcome of complaint monitoring. /li liFor compliance risk events, coordinate and lead the root cause identification, ensuring effective corrective actions for mitigations are captured within QMS documentation (eg CAPA/QI). /li liCoordinate and lead the process mapping and change for the development, revision, and/or maintenance of applicable department SOP’s, job aids, and WI’s. /li liWorks independently, challenges the status quo, identifies gaps, and drives process improvements using Process Excellence tools. Participates and/or leads special projects. /li liExecutes statistical/data-driven processes and documentation to support controlled risk management and decision making. Exhibits strong ability to collaborate and influence Business Partners to ensure appropriate complaint handling and improved complaint management processes. /li liLeads remediation activities and generates the write up and execution of protocols documenting results and report approvals. /li liParticipates and/or leads special projects. Develop and deliver appropriate training (i.e. process, complaint handling, regulatory reporting) to complaint management system end users. /li liFacilitate, lead and collaborate with PQV Reporting and Surveillance on New Product Introduction Processes. /li liInteraction with IT partners and application vendors as required. /li /ul h3Professional experience requirements: /h3 ul li5+ years of related experience including Quality Assurance and/or Quality Control, including experience working in pharmaceutical and/or Medical Device or other related highly regulated industry /li liKnowledge of medical safety environment and regulation /li liPossesses strong organization skills supporting the ability to prioritize and manage workload and meet performance expectations. /li liStrong knowledge of analytical, process mapping, investigation root cause and risk assessment tools /li liGlobal mindset and demonstrated ability to lead change initiatives, project management and develop strong relationships /li liWorking knowledge of and experience with the following regulatory requirements: 21 CFR parts 4, 820, 803, 806, 210, 211, 314, ICH Q10, GDP, GMP, GVP, ISO 13485:2003, ISO 14971:2007/2012, MEDEV 2.12, CMDR and the Medical Device Directive 93/42/EEC /li /ul h3Educational requirements: /h3 pBachelor’s degree or Master’s degree (preferred) in technical, scientific, or engineering disciplines required. Biomedical Engineer, Registered Nurse, Physician Assistant or similar healthcare provider/science license/certification/degree preferred. /p h3Other requirements: /h3 pLocation of Role: EMEA /p pTravel Requirements: This position may require up to 5-10% travel domestically and internationally. /p pbRequired Skills: /b /p pbPreferred Skills: /b /p pBusiness Alignment, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, Human-Centered Design, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP) /p #J-18808-Ljbffr