Quality Control Inspector (m/f/d)

West Pharmaceutical Services, Inc; Eschweiler; Vor Ort; EUR 43.000 - 53.000; Vollzeit

Zusammenfassung

West Pharmaceutical Services, Inc in Eschweiler, Germany invites applications for a Quality Control Inspector (m/f/d). You will inspect raw rubber mixtures, perform visual and dimensional inspections, and document test data in SAP and on the batch card.

We require at least 2 years of cGMP experience, technical training or lab training, and good computer skills. This onsite, fulltime role includes shift work and a 1-year fixed-term contract with a base salary of €48,000 per year.

Qualifikationen

• Minimum 2 years of cGMP experience preferred, ideally in quality.
• Completed technical training or laboratory training as listed.
• Strong computer skills including SAP, Excel, Word and Outlook.

Aufgaben

• Inspect raw rubber mixtures and conduct visual and dimensional inspections.
• Document test data in SAP and on the batch card.
• Block or release batches according to SAP specifications.
• Verify batch card documentation.
• Calibrate and maintain testing equipment.
• Adhere to GMP and ISO guidelines.
• Support production with quality issues.

Kenntnisse

Quality testing

GMP familiarity

MS Office

English desirable

Ausbildung

Technical training / lab training

Tools

SAP

Excel

Word

Outlook

Jobbeschreibung

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Title: Quality Control Inspector (m/f/d)

Requisition ID: 75203

Date: Jul 28, 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.

Job Summary

In this role you will inspect raw rubber mixtures (mixing control) as well as conduct visual and dimensional inspections (in-process control or final control). You will also document test data in SAP and on the batch card.

Contract Details:fulltime, fixed term for 1 year

To be filled:asap

No relocation is provided for this opportunity.

This is an onsite position requiring the team member to be onsite.

Essential Duties and Responsibilities

• Analytical inspection of raw rubber mixtures (mixing control) as well as conducting visual and dimensional inspections (in-process control or final control)
• Documentation of test data in SAP and on the batch card
• Blocking or releasing batches according to specifications in SAP
• Verification of batch card documentation
• Performing special inspections
• Calibration and maintenance of testing equipment
• Adherence to GMP and ISO guidelines
• Supporting production with quality issues
• Forwarding of laboratory samples

Additional Responsibilities

• Cooperative interaction with internal customers within the scope of your responsibilities and adherence to quality standards
• Maintenance of a safe working environment
• Compliance with all relevant regulations, guidelines, work procedures, instructions, and safety rules

Education

• Completed technical training (e.g. Machine and plant operator) or lab training (e.g., CTA, chemical laboratory technician)

Work Experience

• Minimum 2 years of cGMP experience preferred, preferrablywithin a quality field

Preferred Knowledge, Skills and Abilities

• High quality and safety awareness
• A high degree of conscientiousness, reliability, and sense of responsibility
• Experience in quality testing/quality assurance
• Good computer skills (Word, Excel, Outlook, SAP)
• English knowledge desirable
• Assertiveness and decision-making competence
• Willingness to work flexible and ready to work overtime

Shift

• Willingness for shift work in multi-shift operation, including continuous shift systems

Pay Transparency:

The annual base salary for this position is €48,000.00. 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.

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