.Johnson & Johnson is currently seeking a Quality Systems Analyst to join our manufacturing team located in Selzach, Switzerland.At 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 Johnson & Johnson .Are you interested in making a difference in a growing company thriving on a diverse culture, celebrating the uniqueness of our employees, and committed to inclusion?
Apply today for this phenomenal opportunity!What you will be doing: RIM management.Document archiving and electronic recording CAPA/NC responsibility and tracking of relevant activities in ETQ, creating reports.Document management system: creating and changing process descriptions, creating change requests, periodic reviews.Audits: Organizing and accompanying internal and external audits, tracking follow-up measures and documenting them.Processing deviations and supporting team members.Gemba Walks & Audit Readiness: Regular production walks in preparation for audits, tracking of follow-up measures and their documentation.QPR/QSMR: Preparation of management reports per quarter and half-year.Qualifications We would love to hear from YOU if you have the following essential requirements:University/Bachelor's Degree or equivalent experience and supporting education (e.G., Technical Qualification with Further Education).Minimum of two (2) years of experience or equivalent combination of education and experience is required.Related experience in Medical Device or Pharmaceutical environment is preferred.Advanced use of computer and software applications is required, particularly Microsoft PowerPoint, Excel, Word, SharePoint, Outlook, and Teams.Experience with training or coaching others is required.Experience in working in a manufacturing/operations environment is preferred.Knowledge of ISO standards or QS regulations is preferred.Experience in notified body and/or health authority audits is preferred.Experience with root cause investigation, technical writing, change management, and/or risk management is preferred.Experience in Quality Systems process development or enhancement is preferred.Experience in project management is preferred.A certification in process excellence is preferred.REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS Strong verbal and written communication, influencing, and leadership skills; ability to communicate at all levels of the organization, and to interact with and influence cross-functional and cross-business teams to drive results is required