Requisition ID: 70341
Date: Jul 10, 2025
Location:Eschweiler, North Rhine-Westphalia, DE
Department: Quality
Description:
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.

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

• Good knowledge of MS Office applications and SAP.
• Six Sigma training (Green/Black Belt) and training as a Quality Management Representative (QMR) or auditor would be desirable.
• Excellent project management skills.
• Excellent communication and networking skills.
• Independent and solution-oriented work style, assertiveness.
• Good German and English skills, 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.

• Lead and support quality improvement projects using established project management tools.
• Analyze and interpret data, as well as create documentation and reports on quality-relevant process data, identifying corrective and preventive actions.
• Facilitate problem and error analysis, as well as the planning and execution of experiments.
• Manage and improve production and testing processes in close collaboration with production-related areas.
• Responsible for the introduction of quality assurance tools (e.g., FMEA, A3, 8D, Kaizen), including employee training.
• Lead and support Six Sigma and Lean projects, implementing CAPA (Corrective and Preventive Actions).
• Support change control processes and handle process deviation reports.
• Conduct and support internal audits.