Überblick über die Statistik des Gehaltsniveaus für "CAPA Investigator in Deutschland"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, Pharmacology, Pharmacovigilance, Pharmacy, Phase I, pipetting, PMP, Policy, Post Marketing, Postdoctoral research, Post-marketing, Preclinical, Pricing & Reimbursement, Pricing and Reimbursement, PROC, Process Excellence, Procurement, Product Management, Project Leadership, Project Management, PromoMats, Protein Characterisation, protocol development, Protocol writing, PSURs, Public Affairs, publishing, Purchasing, QP, Qualification Visit, Quality Assurance, Quality Control, Quality Management, Quality Management System, Radiology, Randomisation, Randomization, Rave, Reactovigilance, Real World Evidence, Recruitment, Regional Monitoring, Regulatory, Regulatory Operations, Regulatory submissions, Regulatory Systems Management, remote monitoring, RFI, Risk Management, risk-based monitoring, RMA, RMP, SAE, SAE reporting, Sales Inventory, Sample size estimation, Samples, SAS, Scrum, SDS-PAGE, SDTM, Serialisation, Shipments, shipping, Simoa, Site contracts, Site Engagement, site payments, SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary: Responsible for study oversight and delivery management (time, budget, quality) at country level from start-up to closure. Serves as the main point of contact at a country level for internal and external stakeholders. Position Responsibilities: Coordinates country cross functional teams and acts as the main point of contact for a Country with the protocol manager and other global study team members Coordinates with other internal roles in country and site feasibility process, including proposal and validation of country study targets Develops country level patient recruitment strategy & risk mitigation. Coordinates and ensures country level study enrolment targets and timelines are met Leads problem solving and resolution efforts including management of risk, contingencies, issue resolution and escalation to the appropriate stakeholder/s Assessment and set up the of vendors during study start up period (locally) Investigator Meeting participation and preparation Ensures data entered in Clinical Trial Managements Systems is current and complete and access to eDC and vendor systems is available for the Country and clinical trial site personnel Validation of study related materials (i.e. protocol, ICF, patient material) Responsible for preparing country specific documents (e.g. global country specific amendment) Prepares materials for Site Initiation Visits Responsible for verifying and confirming with local team eTMF completeness (Country and Site level) Reviews Site Monitoring visit reports, takes action within the timelines specified and escalates issues and ensures appropriate documentation of issues. Coordination of database locks and query follow up. Ensures timelines are met. Ensure inspection readiness of assigned trials within country. Provide support to Health Authority inspection and pre-inspection activities Coordinates, develops and writes the Corrective Actions / Preventive Actions (CAPA) and ensures implementation for Country audit level findings. Drives CAPA review, implementation and completion. Lead study team meetings locally Reviewing and approving payments (based on GOA) and manage patient compensation claims (if applicable) Management of Site relationships (includes CRO related issues) May conduct Pre-Study Evaluation Visits (PSEVs) and Site Initiation Visits (SIVs) May perform site closure activities, including post-close out May act as point of contact for Sites May support preparing submissions to and obtaining approval from local Health Authorities, Ethics Committees and other relevant instances. Depending on the experience and previous knowledge of the specific candidate, the position may be adjusted to the Senior Level. Senior Level Expectations: Engage with Protocol Manager, line management and/or Head of Clinical Operations to assist in the resolution of complex issues both locally and/or globally Serve as a key resource for colleagues, by providing guidance, leading training and mentoring to other team members through a mentoring process using informal and/or formal presentations (Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned) Position Requirements: Degree Requirements: Bachelors or Masters degree required. Field of study within life sciences or equivalent Experience Requirements: Clinical Trial Manager: Minimum of 4 years' industry related experience Senior Clinical Trial Manager: At least 6 years of industry related experience Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives Key Competency Requirements: Thorough understanding of GCP, ICH Guidelines and Country regulatory environment In depth knowledge and understanding of clinical research processes, regulations and methodology Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management Demonstrated organizational and planning skills and independent decision-making ability Strong organization and time management skills and ability to effectively manage multiple competing priorities Ability of critical thinking and risk analysis. Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels Skilled in the use of technology Good verbal and written communication skills (both in English and local language). Software that must be used independently and without assistance (e.g., Microsoft Suite): Microsoft Suite Clinical Trial Management Systems (CTMS) Electronic Data Capture Systems (eDC) Electronic Trial Master File (eTMF) Based on your function, department or individual position, you will have the opportunity to discuss with your Manager the option to work remotely up to 50% of the time, over a two-week period, with the flexibility to choose the days that align with your collaboration needs. This fixed-term role is meant as maternity cover until 30.06.2025. #LI-Hybrid If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **********. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:0044 BMS GmbH&Co.KGaA Germany

Über HuFriedyGroup:Die HuFriedyGroup ist mit insgesamt über 177 Jahren Erfahrung in der Dentalindustrie weltweit führend in den Bereichen Infektionsprävention, Instrumentenherstellung und Wiederaufbereitung von Instrumenten. Die HuFriedyGroup hilft Zahnärzten dabei, „Best in Practice“ zu sein, indem sie einen geschlossenen „Circle of Protection“ in der Praxis bereitstellt und erstklassige Produkte, Dienstleistungen, Weiterbildungen und Netzwerke bietet, die zu erstklassigen klinischen Leistungen und Ergebnissen führen und auch die Sicherheit für Behandler und Patienten gewährleistet.Als Teil der STERIS Gruppe, mit mehr als 18.000 Mitarbeitenden weltweit, bieten wir zusammen umfassende Produkte und Dienstleistungen für die Gesundheitsbranche. Unsere Aufgabe bei STERIS ist es, unseren Kunden dabei zu helfen, die Welt gesünder und sicherer zu machen.Werde Teil von STERIS! Für unser starkes Team am Standort Emmingen-Liptingen suchen wir eine analytische, kommunikationsstarke Persönlichkeit alsQualitätsingenieur (m/w/d) MedizintechnikDu verantwortest die Aufrechterhaltung, (Weiter-) Entwicklung und kontinuierliche Verbesserung (KVP) unserer Qualitätssysteme gemäß ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR etc. zur Steigerung unserer Produkt- und Servicequalität. Parallel dazu kümmerst Du Dich um die Qualifizierung von Produktionsanlagen und die Prozessvalidierung für drei Standorte (Deutschland, Griechenland, Italien) und arbeitest an Untersuchungen von Beschwerden / CAPAs und der Qualitätsoptimierung bei Lieferanten mit.Deine Aufgaben:Entwickeln und Umsetzen statistisch valider Stichproben- und Versuchspläne, Machbarkeitsstudien, SPC und TrendanalysenDurchführen von Audits des Qualitätssystems, Prüfen gesammelter Daten sowie Erheben statistischer Analysen rund um qualitätssteigernde Prozess- und ProduktanpassungenMonitoring und Bericht der Leistungskennzahlen sowie Initiieren von und / oder Teilnahme an Prozess- und ProduktkorrekturmaßnahmenErstellen, Dokumentieren und Aktualisieren von Arbeitsanweisungen inklusive Unterweisung der Teams in puncto Qualitätsgrundsätze, Korrekturmaßnahmen und gültige statistische TechnikenEnge interdisziplinäre Zusammenarbeit mit verschiedenen Bereichen bei qualitätsbezogenen FragenAufrechterhaltung der Produktintegrität und -qualität, z. B. durch die Bewertung und Disposition nicht konformer Materialien Dein Profil: Technisches oder betriebswirtschaftliches Studium, gern mit relevanten Weiterbildungen rund um QS und QMErfahrung im Projekt- und / oder Qualitätsmanagement, sicherer Umgang mit grundlegenden Qualitätstechniken und -planungen sowie Kenntnisse gültiger Normen, wie ISO 9001 und IATF 16949Gutes Deutsch und Englisch (Wort / Schrift) sowie routinierter Umgang mit MS Office20 % ReisebereitschaftWir bieten Dir:Sicherer Job im KundenserviceEinen unbefristeten und langfristigen Arbeitsplatz in einem globalen UnternehmenAttraktive Vergütung und GleitzeitJährlicher erfolgsbasierter Bonus30 Urlaubstage (plus Sonderurlaubstage)Betriebliche AltersvorsorgeModern WorkplaceErgonomische Arbeitsplätze und moderne ITKostenfreie GetränkeRegelmäßige Team- und Firmenevents (z. B. Weihnachtsfeier, Grillen, Frühlingsfest, Herbstfest, Eisessen)Onboarding & PersonalentwicklungBei uns gehörst Du vom ersten Tag an ins Team, wirst eigenverantwortlich arbeiten und das in einem Team, das sich gegenseitig unterstütztDu erhältst eine umfangreiche EinarbeitungDurch regelmäßige Mitarbeitergespräche und individuelle Personalentwicklungsmaßnahmen wird Deine Entwicklung gefördertJährliche Mitarbeiterumfrage und WeiterbildungenWir bieten Dir eine E-Learning-Plattform, Sprachkurse und vieles mehr Standort Hu-Friedy Mfg. Co., LLC., Villingen-Schwenningen

Über HuFriedyGroup:Die HuFriedyGroup ist mit insgesamt über 177 Jahren Erfahrung in der Dentalindustrie weltweit führend in den Bereichen Infektionsprävention, Instrumentenherstellung und Wiederaufbereitung von Instrumenten. Die HuFriedyGroup hilft Zahnärzten dabei, „Best in Practice“ zu sein, indem sie einen geschlossenen „Circle of Protection“ in der Praxis bereitstellt und erstklassige Produkte, Dienstleistungen, Weiterbildungen und Netzwerke bietet, die zu erstklassigen klinischen Leistungen und Ergebnissen führen und auch die Sicherheit für Behandler und Patienten gewährleistet.Als Teil der STERIS Gruppe, mit mehr als 18.000 Mitarbeitenden weltweit, bieten wir zusammen umfassende Produkte und Dienstleistungen für die Gesundheitsbranche. Unsere Aufgabe bei STERIS ist es, unseren Kunden dabei zu helfen, die Welt gesünder und sicherer zu machen.Werde Teil von STERIS! Für unser starkes Team am Standort Emmingen-Liptingen suchen wir eine analytische, kommunikationsstarke Persönlichkeit alsQualitätsingenieur (m/w/d) MedizintechnikDu verantwortest die Aufrechterhaltung, (Weiter-) Entwicklung und kontinuierliche Verbesserung (KVP) unserer Qualitätssysteme gemäß ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR etc. zur Steigerung unserer Produkt- und Servicequalität. Parallel dazu kümmerst Du Dich um die Qualifizierung von Produktionsanlagen und die Prozessvalidierung für drei Standorte (Deutschland, Griechenland, Italien) und arbeitest an Untersuchungen von Beschwerden / CAPAs und der Qualitätsoptimierung bei Lieferanten mit.Deine Aufgaben:Entwickeln und Umsetzen statistisch valider Stichproben- und Versuchspläne, Machbarkeitsstudien, SPC und TrendanalysenDurchführen von Audits des Qualitätssystems, Prüfen gesammelter Daten sowie Erheben statistischer Analysen rund um qualitätssteigernde Prozess- und ProduktanpassungenMonitoring und Bericht der Leistungskennzahlen sowie Initiieren von und / oder Teilnahme an Prozess- und ProduktkorrekturmaßnahmenErstellen, Dokumentieren und Aktualisieren von Arbeitsanweisungen inklusive Unterweisung der Teams in puncto Qualitätsgrundsätze, Korrekturmaßnahmen und gültige statistische TechnikenEnge interdisziplinäre Zusammenarbeit mit verschiedenen Bereichen bei qualitätsbezogenen FragenAufrechterhaltung der Produktintegrität und -qualität, z. B. durch die Bewertung und Disposition nicht konformer Materialien Dein Profil: Technisches oder betriebswirtschaftliches Studium, gern mit relevanten Weiterbildungen rund um QS und QMErfahrung im Projekt- und / oder Qualitätsmanagement, sicherer Umgang mit grundlegenden Qualitätstechniken und -planungen sowie Kenntnisse gültiger Normen, wie ISO 9001 und IATF 16949Gutes Deutsch und Englisch (Wort / Schrift) sowie routinierter Umgang mit MS Office20 % ReisebereitschaftWir bieten Dir:Sicherer Job im KundenserviceEinen unbefristeten und langfristigen Arbeitsplatz in einem globalen UnternehmenAttraktive Vergütung und GleitzeitJährlicher erfolgsbasierter Bonus30 Urlaubstage (plus Sonderurlaubstage)Betriebliche AltersvorsorgeModern WorkplaceErgonomische Arbeitsplätze und moderne ITKostenfreie GetränkeRegelmäßige Team- und Firmenevents (z. B. Weihnachtsfeier, Grillen, Frühlingsfest, Herbstfest, Eisessen)Onboarding & PersonalentwicklungBei uns gehörst Du vom ersten Tag an ins Team, wirst eigenverantwortlich arbeiten und das in einem Team, das sich gegenseitig unterstütztDu erhältst eine umfangreiche EinarbeitungDurch regelmäßige Mitarbeitergespräche und individuelle Personalentwicklungsmaßnahmen wird Deine Entwicklung gefördertJährliche Mitarbeiterumfrage und WeiterbildungenWir bieten Dir eine E-Learning-Plattform, Sprachkurse und vieles mehr Standort Hu-Friedy Mfg. Co., LLC., Konstanz