Quality Inspector (m/f/d) Incoming Inspection

West Pharmaceutical Services, Inc; Eschweiler; On-site; EUR 45,000 - 57,000; Full time

Job summary

West Pharmaceutical Services, Inc. invites applications for a Quality Inspector (m/f/d) Incoming Inspection at our Eschweiler site. This onsite role within the Quality department starts immediately and requires GMP experience, technical training, and familiarity with SAP and MS Office.

The candidate will perform sampling, material inspections, documentation, and data analyses. A driving license (Class B) is preferred.

Qualifications

• Successful completion of technical training.
• Professional experience in a comparable position, preferably in the pharmaceutical sector or with GMP experience.
• Experience in quality assurance.

Responsibilities

• Sampling according to the sampling plan.
• Forwarding samples to relevant department.
• Inspecting bags and films (dimensions, tensile strength, etc.).
• Conducting color and reactivity testing of raw materials.
• Documentation and filing of test results.
• Posting and releasing raw materials and monitoring testing equipment.

Skills

English (written and spoken)

Independent work

Organizational skills

Education

Technical training

Tools

SAP

Microsoft Word

Microsoft Excel

Job description

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Title: Quality Inspector (m/f/d) Incoming Inspection

Requisition ID: 75956

Date: Sep 30, 2026

Location:

Eschweiler, NW, 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.

Contract Terms: Full-time

Start Date: Immediately

No relocation is provided for this opportunity.

This is an onsite position.

Essential Duties and Responsibilities

• Sampling in accordance with the sampling plan
• Forwarding samples of raw materials, auxiliary materials, and operating supplies to the relevant department
• Inspection of bags and films (dimensions, tensile strength, etc.)
• Color and reactivity testing of raw materials
• Documentation and filing of test results
• Posting and release of raw materials as well as monitoring of testing/measuring equipment
• Handling supplier complaints
• Processing OOS cases, deviations, and process changes
• Preparation of data analyses

Education

• Successfully completed technical training

Work Experience

• Professional experience in a comparable position, preferably in the pharmaceutical sector or with GMP experience
• Experience in quality assurance

Preferred Knowledge, Skills and Abilities

• Proficiency in using Microsoft Office applications (Word, Excel) and SAP
• Independent, structured, and responsible way of working
• Knowledge of GMP-compliant working methods and DIN ISO 9001
• Good written and spoken English skills
• Strong organizational skills and a very precise and careful approach to work
• Class B driver’s license

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

Pay Transparency:

The annual base salary range for this position is€44,700.00 - €56,800.00. 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.

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.