招聘

Quality Engineer EU Operational Programs (m/f/d)
Aachen, North Rhine-Westphalia, Germany
·
On-site
·
Full-time
·
1mo ago
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 Med Tech, 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.As 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.
Job Function: Environmental Health, Safety (EH&S) and Facilities Services (FS)Job Sub Function: Facilities Management & Planning Job Category:Professional All Job Posting Locations:Aachen, North Rhine-Westphalia, Germany Job Description:GERMANStellenbeschreibung – Quality Engineer EU Operational Programs (m/w/d)Überblick der Rolle Derdie Quality Engineer EU Operational Programs (m/w/d) ist verantwortlich für die Schnittstelle zwischen den Abteilungen im Bereich EU Operational Programs und die Abteilung Quality Management.
Zu diesem Bereich gehören die Abteilungen Facility Management, Infrastruktur Projekte und Arbeitssicherheit, Gesundheit und Umwelt (EHS).
Die Rolle kombiniert technisches Verständnis mit Qualitäts- und Sicherheitskompetenz, um Compliance und kontinuierliche Verbesserung sicherzustellen.
Hauptaufgaben & Verantwortlichkeiten1.
Sicherung von Qualitäts-Compliance in den Abteilungen Facility Management, Infrastruktur- und Bauprojekten und EHS (Environment, Health & Safety):Qualitäts- und Compliance‑Begleitung technischer Betriebsprozesse (Versorgungstechnik, HLK, Reinräume, Druckluft, technische Gase, etc…).Sicherstellung der Dokumentation und Nachverfolgung von Wartungs‑, Prüf‑ und Kalibrieraktivitäten gemäß interne SOPs und regulatorischen Anforderungen.
Bewertung technischer Störungen und Ableitung von CAPA‑Maßnahmen gemeinsam mit Quality, Engineering und Operations.
Sicherstellen, dass alle Facilities, Bau‑, Umbau‑ und Infrastrukturmaßnahmen den Qualitäts‑, GMP-, ISO- und internen Standards entsprechen.
Qualitätsanforderungen in Projektplanungen, Designspezifikationen und technischen Konzepten definieren und prüfen.
Unterstützung bei Audits und Behördeninspektionen.2.
Dokumentation, Compliance & Prozessmanagement:Erstellung und Pflege qualitätsrelevanter Dokumentationen (Quality Notes, Deviations, Non-Conformances, CAPAs, ….).Erstellung, Pflege und kontinuierliche Verbesserung von SOPs, technischen Leitlinien, und Prüfplänen.
Sicherstellen der Einhaltung interner Standards, globaler Richtlinien und externer Vorschriften.
Mitwirkung an kontinuierlichen Verbesserungsprozessen und Lean‑/Six‑Sigma‑Aktivitäten.3.
Untersuchungen & CAPA-Management Durchführung technischer Root‑Cause‑Analysen bei Mängeln oder Störungen im Facility-, Bau- oder EHS‑Kontext.
Erstellen, Tracken und Bewerten von CAPAs sowie deren Wirksamkeitsprüfung.
Durchführen oder Begleiten von qualitätsbezogene Risikoanalysen und Gefährdungsbeurteilungen.Förderung der Zuverlässigkeit durch systematische Lessons‑Learned‑Prozesse.4.
Schnittstellenmanagement Enge Zusammenarbeit mit Engineering, Facility Management, EHS, Produktion, externen Partnern und globalen Qualitätsfunktionen.
Sicherstellen einer klaren Kommunikation und eines strukturierten Informationsflusses in multidisziplinären Teams.
Qualifikationen & Anforderungen Fachlich Abgeschlossenes Studium im Bereich Ingenieurwesen (z. B.
Versorgungstechnik, Gebäudetechnik, Umwelttechnik, Maschinenbau, Elektrotechnik) oder vergleichbare Qualifikation.
Erfahrung im Qualitätsmanagement, idealerweise in regulierten Industrien (Med Tech, Pharma, Biotech, High-Tech).Kenntnisse im Facility Management, Bauprojekten, technischer Gebäudeausrüstung oder Reinraumumgebung von Vorteil.ausgeprägtes technisches Verständnis Verständnis relevanter Normen/Regulatorien (z. B. ISO 9001, ISO 14001, ISO 45001, GMP).Erfahrung mit CAPA, RCA, Change Control, Audits und Dokumentationssystemen.
Persönlich Analytische Denkweise und ausgeprägte Problemlösungsfähigkeiten.
Starke Kommunikations- und Koordinationsfähigkeiten in interdisziplinären Teams.
Strukturierte Arbeitsweise, hohe Qualitätsorientierung und Verantwortungsbewusstsein.Fähigkeit, technische Prozesse kritisch zu hinterfragen und nachhaltig zu verbessern.
Hohe Flexibilität und ausgeprägte Teamfähigkeit Die erwartete Basisvergütung für diese Position beträgt 62.500 EUR bis 97.865 EUR.ENGLISHJob Description – Quality Engineer EU Operational Programs (m/f/d)Role Overview The Quality Engineer EU Operational Programs (m/f/d) is responsible for the interface between the departments within EU Operational Programs and the Quality Management department.
This includes Facility Management, Infrastructure Projects, and Environment, Health & Safety (EHS).
The role combines technical understanding with quality and safety expertise to ensure compliance and continuous improvement.
Main Tasks & Responsibilities1.
Ensuring Quality Compliance in Facility Management, Infrastructure/Construction Projects, and EHSQuality and compliance support for technical operational processes (utilities, HVAC, cleanrooms, compressed air, technical gases, etc.).Ensuring documentation and follow-up of maintenance, inspection, and calibration activities in accordance with internal SOPs and regulatory requirements.
Assessment of technical malfunctions and derivation of CAPA measures together with Quality, Engineering, and Operations.
Ensuring that all facilities, construction, renovation, and infrastructure measures comply with quality, GMP, ISO, and internal standards.
Defining and reviewing quality requirements in project planning, design specifications, and technical concepts.
Supporting audits and regulatory inspections.2.
Documentation, Compliance & Process Management Creating and maintaining quality-relevant documentation (Quality Notes, Deviations, Non-Conformances, CAPAs, etc.).Creating, maintaining, and continuously improving SOPs, technical guidelines, and test plans.
Ensuring compliance with internal standards, global guidelines, and external regulations.
Participation in continuous improvement processes and Lean/Six Sigma activities.3.
Investigations & CAPA Management Conducting technical root cause analyses for deficiencies or malfunctions in Facility, Construction, or EHS contexts.
Creating, tracking, and evaluating CAPAs, including effectiveness checks.
Conducting or supporting quality-related risk analyses and hazard assessments.
Promoting reliability through systematic lessons-learned processes.4.
Interface Management Close collaboration with Engineering, Facility Management, EHS, Production, external partners, and global quality functions.
Ensuring clear communication and structured information flow within multidisciplinary teams.
Qualifications & Requirements Technical Completed degree in engineering (e.g., building services engineering, facility engineering, environmental engineering, mechanical engineering, electrical engineering) or equivalent qualification.
Experience in quality management, ideally in regulated industries (Med Tech, pharma, biotech, high-tech).Knowledge in facility management, construction projects, technical building equipment, or cleanroom environments is an advantage.
Strong technical understanding.
Understanding of relevant standards/regulations (e.g., ISO 9001, ISO 14001, ISO 45001, GMP).Experience with CAPA, RCA, Change Control, audits, and documentation systems.
Personal Analytical mindset and strong problem-solving skills.
Strong communication and coordination skills in interdisciplinary teams.
Structured working style, high quality orientation, and sense of responsibility.
Ability to critically question and sustainably improve technical processes.
High flexibility and strong team orientation.
The anticipated base pay range for this position is 62.500 EUR to 97.865 EUR.
Required Skills:
Preferred Skills:Access Control (AC), Business Behavior, Conflict Resolution, Data-Driven Decision Making, Disruptive Innovations, Facility Management, Facility Management Software, Organizing, Premises Management, Proactive Behavior, Problem Solving, Project Reporting, Security Planning, Service Excellence, Standard Operating Procedure (SOP), Subject Matter Experts (SME) Collaboration
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关于Johnson & Johnson

Johnson & Johnson
PublicJohnson & Johnson (J&J) is an American multinational pharmaceutical, biotechnology, and medical technologies corporation headquartered in New Brunswick, New Jersey, and publicly traded on the New York Stock Exchange.
10,001+
员工数
New Brunswick
总部位置
$400B
企业估值
评价
4.0
10条评价
工作生活平衡
3.8
薪酬
4.2
企业文化
4.1
职业发展
3.5
管理层
4.3
75%
推荐给朋友
优点
Supportive and approachable management
Excellent benefits and compensation
Flexible work arrangements and work-life balance
缺点
High-pressure and demanding work environment
Slow bureaucratic processes
Heavy workload and high expectations
薪资范围
2,250个数据点
Junior/L3
Senior/L5
Junior/L3 · Analyst
177份报告
$93,472
年薪总额
基本工资
$85,723
股票
-
奖金
$7,749
$59,968
$146,648
面试经验
7次面试
难度
3.0
/ 5
时长
14-28周
面试流程
1
Application Review
2
HR Screen
3
Pre-recorded/Video Interview
4
Technical/Panel Interview
5
Final Interview
6
Offer
常见问题
Behavioral/STAR
Technical Knowledge
Past Experience
Culture Fit
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