West Pharmaceutical Services in Eschweiler sucht einen engagierten Quality Engineer (m/w/d) zur Verstärkung des Teams. Der Fokus der Stelle liegt auf der Leitung und Unterstützung von Qualitätsverbesserungsprojekten, der Analyse von Daten und der Einführung von Qualitätssicherungswerkzeugen. Enge Zusammenarbeit mit produktionsnahen Bereichen sowie die Durchführung interner Audits gehören ebenfalls zu den Aufgaben. Wenn Sie über Kenntnisse im pharmazeutischen Umfeld und Erfahrung im Qualitätsmanagement verfügen, bietet West eine inklusive Arbeitsumgebung mit vielfältigen Entwicklungsmöglichkeiten.
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Essential Duties and Responsibilities
- Drive and support quality enhancement projects leveraging established project management tools.
- Analyze and interpret data, generating documentation and reports on quality-relevant process data, identifying corrective and preventive actions.
- Facilitate problem and error analysis, and oversee the planning and execution of experiments.
- Manage and refine production and testing processes through close collaboration with production-related areas.
- Implement quality assurance tools (e.g., FMEA, A3, 8D, Kaizen), including employee training programs.
- Spearhead and support Six Sigma and Lean initiatives, implementing CAPA (Corrective and Preventive Actions).
- Support change control processes and manage process deviation reports.
- Execute and support internal audits.
Education
- Successfully completed studies in engineering or natural sciences.
Work Experience
- Experience in the pharmaceutical environment or in quality-related fields, including knowledge of cGMP (current Good Manufacturing Practices).
Preferred Knowledge, Skills and Abilities
- Proficient in MS Office applications and SAP.
- Six Sigma training (Green/Black Belt) and certification as a Quality Management Representative (QMR) or auditor are advantageous.
- Exceptional project management skills.
- Strong communication and networking abilities.
- Independent and solution-driven work ethic, with assertiveness.
- Excellent German and English language proficiency, both spoken and written.
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.
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