Quality Engineer Incoming Inspection (m/f/d)

West Pharmaceutical Services; Eschweiler; Vor Ort; EUR 60.000 - 76.000; Vollzeit

Zusammenfassung

West Pharmaceutical Services in Germany seeks a Quality Management professional to strengthen our local quality program. This onsite role focuses on materials quality, supplier management, and audits in a GMP environment.

You will lead lean improvements, support ISO and customer audits, and collaborate across departments to ensure compliant processes. Fluent German and English are essential, as is a technical degree and 3+ years of pharma quality experience.

Qualifikationen

• Degree in a technical field.
• Lean management or project management training is desirable.
• At least 3 years of quality management experience (pharma/GMP preferred).

Aufgaben

• Execute local optimization projects on raw materials and packaging.
• Represent local interests in global projects.
• Lead supplier meetings.
• Prepare for and support audits (customer and ISO).
• Implement actions from audits with stakeholders.
• Analyze and restructure internal workflows via lean management.
• Collaborate with other departments to drive quality initiatives.
• Manage approved suppliers and approve/block local suppliers.
• Collect and trend quality metrics for other departments.
• Prepare complaints and quality notifications in English and German.
• Support OOS related actions with reports.
• Execute and follow up on internal quality audits.
• Prepare deviations and process changes with trend analysis.

Kenntnisse

German language

English language

Communication skills

Teamwork

Assertiveness

Conflict management

Ausbildung

Technical degree

Lean/project management training

Tools

MS Office

SAP

Jobbeschreibung

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?

Description

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.

No relocation is provided for this opportunity.

This is an onsite position, requiring the team member to be onsite 5 days a week.

Essential Duties And Responsibilities

• Execution of local optimization projects related to raw materials and packaging materials
• Representation of local interests in global projects
• Participation in / leadership of meetings with suppliers
• Preparation for and support of customer and ISO audits
• Implementation of actions resulting from audit processes with internal and external stakeholders
• Analysis and restructuring of internal workflows from a lean management perspective
• Collaboration with other departments to drive quality initiatives, systems, and methods to achieve quality objectives
• Responsible for the system-based management of approved suppliers, including approval / blocking of local suppliers
• Collection, analysis, evaluation, and trending of quality‑relevant metrics for other departments
• Preparation of complaints and quality notifications in English and German
• Support for actions within the scope of Out‑Of‑Specification (OOS) cases related to raw materials and packaging materials, including preparation of necessary reports and documentation
• Execution, documentation, evaluation, and follow‑up of actions resulting from internal quality audits
• Preparation of deviations, OOS cases, and process changes, including trend analysis and initiation of improvement measures in the area of raw materials and packaging materials

Education

• Successfully completed degree in a technical field
• Training in lean management and/or project management is desirable

Work Experience

• At least 3 years of professional experience in quality management, preferably in the pharmaceutical sector or with GMP experience

Preferred Knowledge, Skills And Abilities

• Very good written and spoken German and English skills
• Solid knowledge of MS Office
• Knowledge of statistical methods and SAP is desirable
• Strong communication and teamwork skills
• Very strong assertiveness and conflict management skills

License and Certifications

• Certification as a Quality Management Representative (QMR) is desirable, or willingness to obtain it

Pay Transparency

The annual base salary range for this position is €60,016.00 – €76,384.00. Total target compensation is determined using objective and gender‑neutral criteria, including relevant experience, qualifications, skills, market benchmarks, geographic location, and the scope and responsibilities of the role. This position may be eligible for variable compensation and other incentive programs in accordance with the terms of the applicable plans within the country of employment. In addition, team members are eligible to participate in the company’s benefits and total rewards programs applicable to their location and employment status.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [e-mail] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.