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Quality Control Inspector (m / f / d)

Quality Control Inspector (m / f / d)

West Pharmaceutical ServicesEschweiler, North Rhine-Westphalia, DE
Vor 20 Tagen
Stellenbeschreibung

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

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

  • Completed technical training (e.g. Machine and plant operator) or lab training (e.g., CTA, chemical laboratory technician)
  • 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)
  • Assertiveness and decision-making competence
  • Willingness to work flexible and ready to work overtime
  • Willingness for shift work in multi-shift operation, including continuous shift systems
  • English knowledge desirable
  • Work Experience

  • Minimum 2 years of cGMP experience preferred, preferrably 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. #LI-KS1

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