Quality Control Inspector (m/f/d)

West Pharmaceutical Services; Eschweiler; Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A leading healthcare solutions provider is looking for a Quality Control Inspector in Eschweiler, Germany. This full-time, on-site position involves inspecting raw rubber mixtures and conducting quality inspections to ensure adherence to GMP and ISO guidelines. The ideal candidate should have completed technical training, preferably possess 2 years of cGMP experience, and demonstrate strong quality awareness. Join a dedicated team committed to improving patient lives while enjoying opportunities for professional growth.

Qualifikationen

• Minimum 2 years of cGMP experience preferred, preferably within a quality field.
• English knowledge desirable.

Aufgaben

• Inspect raw rubber mixtures and conduct visual and dimensional inspections.
• Document test data in SAP and on the batch card.
• Verify and block or release batches according to specifications.

Kenntnisse

High quality and safety awareness

Good computer skills (Word, Excel, Outlook, SAP)

Experience in quality testing/quality assurance

Assertiveness and decision-making competence

Willingness to work flexible hours

Ausbildung

Completed technical training (e.g. Machine and plant operator)

Tools

SAP

Jobbeschreibung

No relocation is provided for this opportunity.

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

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 Details: fulltime, fixed term for 1 year

To be filled: asap

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.

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, preferrably within 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

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 and/or a pre‑employment drug screening.