PeopleShare has an opening for a QA Analyst/Process Inspector in Camden, NJ and we are looking for candidates with a background in manufacturing, quality assurance, and working with Microsoft Excel.
Title: QA Analyst/Process Inspector
Location: Camden, NJ 08105
Schedule: Monday-Friday 6:30 AM - 3:00 PM
Salary: Full-time, $20/hr
Overview:
The QA Analyst/Process Inspector is responsible for conducting inspections of materials, subassemblies and finished product, as well as, evaluating quality data collected throughout the manufacturing process and the field to determine root cause, trends, failure rate, etc. Conducting incoming, in-process and final QA inspections to verify product meets specifications. Evaluations include visual and physical examination, functional testing, data analysis and dimensional analysis using a variety of equipment, software and gauges.
Responsibilities:
- Analyze manufacturing and field data to determine trends, product conformance, costs of nonconformance, failure rate and on-time delivery.
- Drive corrective & preventive actions to resolution.
- Work as team member to continually improve quality management system.
- Must be able to accurately read/interpret engineering drawings and other similar specifications.
- Identify procedural deficiencies & Update quality system procedures as needed.
- Conduct and document process & material inspections in accordance with specifications.
- Samples product and labels according to established sampling plans and documented instructions.
- Identifies and segregates nonconforming materials in accordance with documented instructions
- Accurate and timely completion of inspection reports, NC reports, logs and other records is required.
- Works in an organized manner at all times, to ensure lot traceability and to prevent mix-ups.
- Adheres to all regulations, safety rules/practices and organizational policies and procedures.
- Project and/or responsibility tasks oriented to assist engineering with continuous improvement activities.
Secondary Responsibilities:
- Project responsibilities, to be defined by management, to meet business needs; tasks to assist manufacturing, engineering and other personnel with D&D projects, validation, verification, etc.
Requirements:
- Associates degree or technical certification desired.
- A minimum of 3 years’ experience working in a manufacturing or similar is required.
- Must have computer skills, including MS Word, MS Outlook, Excel, and PowerPoint. Access skills desired. Excel skills required include formula creation/modification, filters, sorting, data validation and conditional formatting.
- Medical device/pharma/ISO experience highly desired.
- Good oral and writing skills required. Must be able to speak, read and write the English language and perform basic mathematical calculations.
- Competent with inspection techniques and common inspection equipment and gauges, including calipers, micrometers, scales, multi-meters, and pressure gauges, is required. Precision/Vision measurement system experience desired.
Physical Requirements:
- Must be able to lift up to 50 lbs.
- Must be able to stand or sit for an extended period of time.
- Must be able to push/pull carts loaded with boxes/products for evaluation/inspection.
- Vision: Must be able to distinguish colors and have close visual acuity to perform activities such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving
small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication parts at distances close to the eyes.
Work Environment:
- Office, lab, production and warehouse setting.
