Quality Control Inspector (m/f/d)

West Pharmaceutical Services; Eschweiler; Vor Ort; EUR 35.000 - 55.000; Vollzeit

Zusammenfassung

An established industry player is seeking a dedicated Quality Control Inspector to ensure the highest standards in raw rubber inspections. In this role, you'll be vital in conducting thorough inspections, documenting data accurately, and supporting production quality. Your attention to detail and commitment to safety will help maintain compliance with GMP and ISO guidelines. Join a diverse and inclusive team that values your contributions and offers opportunities for growth and development. If you're passionate about quality assurance and ready to make a difference, this position is an excellent fit for you.

Qualifikationen

• Completed technical or lab training with a focus on quality assurance.
• Minimum 2 years of cGMP experience preferred in a quality field.

Aufgaben

• Inspect raw rubber mixtures and conduct visual inspections.
• Document test data in SAP and manage batch documentation.
• Support production with quality issues and maintain testing equipment.

Kenntnisse

Analytical Inspection

Quality Testing

Documentation Skills

Attention to Detail

Customer Service

Problem-Solving

Ausbildung

Technical Training (Machine and Plant Operator)

Lab Training (CTA, Chemical Laboratory Technician)

Tools

SAP

Microsoft Word

Microsoft Excel

Microsoft Outlook

Jobbeschreibung

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.

Essential Duties and Responsibilities

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

Additional Responsibilities

1. Provide a “Customer Service” attitude when interacting with internal customers while accomplishing work, production, and achieving quality standards.
2. Maintain a clean, orderly, and safe workstation and environment at all times.
3. Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
4. Keep current with new GMP compliance guidance and internal QA procedures

Education

1. Completed technical training (e.g. Machine and plant operator) or lab training (e.g., CTA, chemical laboratory technician)
2. High quality and safety awareness
3. A high degree of conscientiousness, reliability, and sense of responsibility
4. Experience in quality testing/quality assurance
5. Good computer skills (Word, Excel, Outlook, SAP)
6. Assertiveness and decision-making competence
7. Willingness to work flexible and ready to work overtime
8. Willingness for shift work in multi-shift operation, including continuous shift systems
9. English knowledge desirable

Work Experience

1. Minimum 2 years of cGMP experience preferred, preferably within a quality field

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.