QUALITY INSPECTOR (for incoming RAW Materials & Finished Product) MUST have experience with tes[...]

Palisades Dental, LLC - Impact Air 45; Englewood (NJ); Sur place; USD 45 000 - 65 000; Plein temps

Avantages offerts par ce poste

Medical Benefits package

Confidential information handling

Résumé du poste

Palisades Dental, LLC - Impact Air 45 is seeking a Quality Inspector based in Englewood, NJ. The role involves inspecting incoming raw materials and finished products using various testing equipment.

Candidates must have experience with inspection tools and relevant quality experience, along with knowledge of cGMP and FDA compliance. The position offers a medical benefits package and a Monday to Friday schedule from 7:30 AM to 4:00 PM.

Qualifications

• 2 years of relevant quality experience preferred.
• Experience with FDA compliance regulations is a plus.

Responsabilités

• Inspect all incoming raw materials and finished products.
• Report and trend quality data for inspection results.
• Ensure compliance with cGMP practices.

Connaissances

Quality inspection

Testing equipment

cGMP procedures

FDA compliance

Outils

Calipers

Micrometers

Optical comparator

Gauges

Description du poste

QUALITY INSPECTOR (for incoming RAW Materials & Finished Product) MUST have experience with testing equipment!

• Full-time

Palisades Dental, LLC is a Medical Device Manufacturer and Distributor located in Englewood, NJ with products available across the US.

The Quality INSPECTOR position will be responsible for inspection of all incoming raw materials and finished products. Tasks will require use of calipers, micrometers, gauges, optical comparator, drawing comparisons and other inspection tools - candidate MUST have experience with relevant equipment.

Report, analyze and trend quality data (e.g. non-conforming material and inspection results). Work directly with suppliers to address quality concerns and assess performance. Responsible for specific quality programs as assigned, other related responsibilities as follows:

• Ensures company standard practices and cGMP procedures are followed.
• Issue Batch Records to production and Finished Good inspection records to Operations
• Maintains SOP binders and updates such through approved Change Controls.
• Participate in internal and external audit process
• Inspect and evaluate all incoming components and labeling
• Inspection and testing of finished goods
• Authorize release of Quarantined components for production use
• Responsible for calibration schedules for testing and production equipment
• PROVIDE SALARY HISTORY TO BE CONSIDERED

Relevant quality experience along with cGMP and 2 years experience preferred.

Experience with FDA compliance regulations a plus

To be considered you MUST provide the following:

• Current resume
• Full Salary History

Salary & Benefits

• Salary will be based on experience
• Medical Benefits package available
• Schedule – F/T Monday to Friday 7:30 to 4:00 pm

All your information will be kept confidential according to EEO guidelines.