Manager, GD Quality Management

pAt Johnson Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 h3Job Function /h3 pQuality /p h3Job Sub Function /h3 pBusiness Process Quality /p h3Job Category /h3 pProfessional /p h3All Job Posting Locations: /h3 pZug, Switzerland /p h3Job Description /h3 h3Manager, Process Personnel Qualification Management Expert /h3 h3Join Johnson Johnson's RD Quality Team! /h3 pAre you eager to learn, collaborate, and make a positive impact? As a Manager in Process Personnel Qualification Management, you will drive compliance and quality excellence in the pharmaceutical industry. In this role, you will lead process improvement projects and use the latest digital tools to support the transformation from traditional processes and training into a data centric content and qualification management system. /p h3What You'll Do /h3 ul liYou will lead process and training related projects, including process development, mapping, and training development/qualification and delivery. /li liYou will be a vital quality partner for Global Development, promoting collaboration and serving as a link between business partners, quality groups, and governance. This role ensures that our GxP Quality Framework effectively adapts to both business and regulatory changes in a proactive manner. /li liYour ability to manage tasks, timelines, and deliverables will be crucial for achieving successful project outcomes. Additionally, you will address issues, managing risks, and providing timely updates to management and business owners regarding project progress. /li liYou will support the implementation of our digital transformation roadmap, driving our evolution towards data-centric content and a robust qualification management system. /li liYou may support or lead additional projects, meetings, audits/inspections, etc. as directed. /li /ul h3Qualifications And Required Knowledge /h3 ul liEducation: At a minimum a Bachelor’s degree in Science or Business is required (Masters degree is preferred). /li liExperience: A minimum of 5 years in a medium to large-scale matrix organization, with at least 5 years focused on pharmaceutical/device compliance. Preferred experience includes process design and training design. /li liCommunication Skills: Exceptional proficiency in both oral and written English communication, with a talent for articulating complex ideas in a clear and effective manner. /li liRegulatory Knowledge: Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations and guidelines, coupled with experience in the life sciences industry's regulatory framework. /li liProject Management Skills: Demonstrated expertise in managing intricate projects and fostering collaboration among diverse teams and departments. /li liAnalytical Skills: Keen attention to detail and robust analytical thinking abilities to evaluate business processes and implement improvements. /li liLeadership and Networking: Established track record in personal leadership, building relationships, working autonomously, and cultivating an inclusive work atmosphere that values diversity. /li /ul h3Preferred Skills: /h3 ul liBusiness Process Management (BPM) /li liBusiness Requirements Analysis /li liCoaching /li liCompliance Management /li liCross-Functional Collaboration /li liData Savvy /li liFact-Based Decision Making /li liISO 9001 /li liLeverages Information /li liProcess Governance /li liProcess Improvements /li liProcess Optimization /li liQuality Control (QC) /li liQuality Standards /li liQuality Validation /li liStakeholder Engagement /li liStandard Operating Procedure (SOP) /li liTactical Thinking /li liTechnical Credibility /li /ul #J-18808-Ljbffr