Receiving Inspector II
Spectraforce
Newark, Delaware
8 days ago
Job Description
Position Title: Receiving Inspector II
Work Location: Newark DE 19702
Assignment Duration: 6 Months
Work Schedule: M-F; 7:00AM to 4:00PM (Possible OT)
Work Arrangement: Onsite
Position Summary:
Performs inspection of purchased parts, materials, components, and equipment as materials are received from vendors or subcontractors. Determines or assists in determining methods, sequences and procedures necessary for inspection. Works from drawings, sketches and specifications. Adapts inspection measuring devices and procedures where necessary.
Works on assignments that are semi routine in nature but recognizes the need for occasional deviation from accepted practice.
Background & Context:
Supports material receipt, verification, and quality documentation processes in a manufacturing environment that operates under FDA-regulated medical device standards.
Key Responsibilities:
• Receive incoming material and perform necessary verifications such as visual and dimensional inspections, quantity verifications and comparing parts against purchase orders, Bills of Material (BOM), component specifications and inspection checklists.
• Perform supplier documentation review for accuracy and completions. Verify requirements including certifications and specifications.
• Document the acceptability conditions of incoming material in the PLM (Product Lifecycle Management) system.
• Generate NCE’s and participate in the MRB process.
• Communicate with internal customers and suppliers to resolve inspection discrepancies.
• Responsible for effective material status control at all times.
• Understand and ensure daily inspection priorities are met. Otherwise maintain and execute FIFO within work area. Move materials as required using standard material handling equipment. Release product in ERP system to released location.
• Perform first article inspections.
• Review quality alerts, corrective actions, and containment activities.
• Complete all training requirements in a timely manner and maintain accurate training records.
• Regular and punctual attendance. Ability to adhere to standardized production schedule for position and ability to work overtime to support production needs as necessary.
Qualification & Experience:
• Preferred Minimum Non-Technical Degree: High School (H.S./GED) or Associate Degree
• Preferred Minimum Non-Technical Degree: 1-2 Years
• Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial.
• Experience in FDA regulated medical device environment is beneficial.
• Strong understanding and working knowledge of Microsoft Office programs including Excel, Work, SharePoint and OneDrive, data entry and ERP Systems
• Ability to read, understand, and follow all written procedures.
• Strong effective communication skills, both written and verbal
• Ability to work both independently and as a member of a team.
• High-level of attention to detail and focus on quality.
• Detail oriented and accurate.
• Ability to use quality control tools such as measuring tapes, calipers, micrometers, scales, gauges, microscopes, etc.
• Knowledge of product specifications
• Ability to read and interpret basic schematics, blueprints, part lists and other technical data.
• Quality assurance experience in a manufacturing environment
• Understanding of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices)
• Ability to operate a forklift and other material handling equipment.
• Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) is beneficial.
• ASQ Certified Quality Inspector is beneficial.
Working Conditions & Physical Demands:
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety Shoes with Impact and Compression Protection Must be worn in designated areas.
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 22.40/hr.
Work Location: Newark DE 19702
Assignment Duration: 6 Months
Work Schedule: M-F; 7:00AM to 4:00PM (Possible OT)
Work Arrangement: Onsite
Position Summary:
Performs inspection of purchased parts, materials, components, and equipment as materials are received from vendors or subcontractors. Determines or assists in determining methods, sequences and procedures necessary for inspection. Works from drawings, sketches and specifications. Adapts inspection measuring devices and procedures where necessary.
Works on assignments that are semi routine in nature but recognizes the need for occasional deviation from accepted practice.
Background & Context:
Supports material receipt, verification, and quality documentation processes in a manufacturing environment that operates under FDA-regulated medical device standards.
Key Responsibilities:
• Receive incoming material and perform necessary verifications such as visual and dimensional inspections, quantity verifications and comparing parts against purchase orders, Bills of Material (BOM), component specifications and inspection checklists.
• Perform supplier documentation review for accuracy and completions. Verify requirements including certifications and specifications.
• Document the acceptability conditions of incoming material in the PLM (Product Lifecycle Management) system.
• Generate NCE’s and participate in the MRB process.
• Communicate with internal customers and suppliers to resolve inspection discrepancies.
• Responsible for effective material status control at all times.
• Understand and ensure daily inspection priorities are met. Otherwise maintain and execute FIFO within work area. Move materials as required using standard material handling equipment. Release product in ERP system to released location.
• Perform first article inspections.
• Review quality alerts, corrective actions, and containment activities.
• Complete all training requirements in a timely manner and maintain accurate training records.
• Regular and punctual attendance. Ability to adhere to standardized production schedule for position and ability to work overtime to support production needs as necessary.
Qualification & Experience:
• Preferred Minimum Non-Technical Degree: High School (H.S./GED) or Associate Degree
• Preferred Minimum Non-Technical Degree: 1-2 Years
• Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial.
• Experience in FDA regulated medical device environment is beneficial.
• Strong understanding and working knowledge of Microsoft Office programs including Excel, Work, SharePoint and OneDrive, data entry and ERP Systems
• Ability to read, understand, and follow all written procedures.
• Strong effective communication skills, both written and verbal
• Ability to work both independently and as a member of a team.
• High-level of attention to detail and focus on quality.
• Detail oriented and accurate.
• Ability to use quality control tools such as measuring tapes, calipers, micrometers, scales, gauges, microscopes, etc.
• Knowledge of product specifications
• Ability to read and interpret basic schematics, blueprints, part lists and other technical data.
• Quality assurance experience in a manufacturing environment
• Understanding of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices)
• Ability to operate a forklift and other material handling equipment.
• Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) is beneficial.
• ASQ Certified Quality Inspector is beneficial.
Working Conditions & Physical Demands:
The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
• Sit; use hands to finger, handle or feel objects, tools, or controls.
• Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts, vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety Shoes with Impact and Compression Protection Must be worn in designated areas.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 22.40/hr.