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Millipore Quality Control Inspector in Allentown, Pennsylvania

The Quality Control Inspector at MilliporeSigma is Allentown, PA is responsible for the quality control incoming inspection of finished good products from contracted manufacturers. Post-inspection processing will include releasing products through inventory software, Oracle or SAP, and filing associated quality records. Position responsibilities to include: Conducting incoming visual inspections of finished good products in accordance with documented specifications and inspection cardsAssisting in processing vendor's documentation (certificates of analysis) to the website for finished good product releasesReleasing finished goods products in Oracle or SAPInitial evaluation of customer returned products to approved purchase specifications and drawingsSupporting inventory evaluation requests and reworking product, as neededAssisting QA/QC/RA teams with the ongoing training of quality procedures, techniques and concepts in accordance with the MilliporeSigma Quality SystemsWorking with in-house personnel and contract manufacturers to resolve quality issues through techniques and evaluation criteria for processes and productsPeriodic cleaning and maintenance of QC Inspection area to ensure desks, workstations and room remain clean, organized and presentable for planned or unplanned tours, visits and audits; this includes developing and maintaining the quality record filing system for ease of identification and retrieval. Periodic preparation, storage and retrieval of quality records is neededAdditional responsibilities may include calibration management, Dock-to-Stock (DTS) periodic reviews, and multi-site QC Hold release supportOther duties as assigned

Physical Attributes:

Sit at a computer for long periods of time (up to 3 hours) Ability to lift 25 lbs.Ability to physically inspect products in a warehouse setting

Who You Are:

Minimum Qualifications:

High School Diploma or GED and 1+ year of Quality Control Inspection experience in a chemical manufacturing or processing environment, or at a medical device or pharmaceutical company

Preferred Qualifications:

Excellent computer skills; experience with Oracle or SAP (particularly the Quality Module) and Microsoft Word, Excel and OutlookSelf-motivated and detail oriented with a focus on continuous improvementKnowledge of ISO 9001, cGMP, QSR and Responsible Care Ability to interact in a positive and effective manner with other company departments to solve problems and create more effective processes and procedures Excellent communication skills, both verbal and written, and good mathematics skills

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