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Form of workWork Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
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 cards
- Assisting in processing vendor's documentation (certificates of analysis) to the website for finished good product releases
- Releasing finished goods products in Oracle or SAP
- Initial evaluation of customer returned products to approved purchase specifications and drawings
- Supporting inventory evaluation requests and reworking product, as needed
- Assisting QA/QC/RA teams with the ongoing training of quality procedures, techniques and concepts in accordance with the MilliporeSigma Quality Systems
- Working with in-house personnel and contract manufacturers to resolve quality issues through techniques and evaluation criteria for processes and products
- Periodic 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 needed
- Additional responsibilities may include calibration management, Dock-to-Stock (DTS) periodic reviews, and multi-site QC Hold release support
- Other 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 Outlook
- Self-motivated and detail oriented with a focus on continuous improvement
- Knowledge 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
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html
