Quality Control Inspector II

Job Description

Position Title:

Quality Control Inspector II

Work Location:

Newark

DE 19702

Assignment Duration:

6 Months

Work Schedule:

M-F; 2nd

SHIFT:

2:30 PM to 11:00 PM (Initial training required on first shift for approximately the first 3 to 4 weeks; First shift training hours are approximately 6:00 AM to 2:30 PM)

Work Arrangement:

100%

Onsite Position Summary:

Performs inspections, testing, and sampling procedures for product manufacturing. Includes packaging line and incoming material checks. Reviews and releases Device History Records. May assist with validation or troubleshooting of testing methods.

• Routine assignments with limited judgment
• Acquires job skills and follows company procedures
• Works under moderate supervision

Background & Context:

QC Inspector II role within a regulated medical device manufacturing environment. Work is 100 percent on site. Responsibilities include device history record review, documentation verification, physical inspection, and final quality signoff. Three total openings. Contingent staff augmentation assignment.

Key Responsibilities:

• Maintain and promote a safe work environment
• Conduct inspections of in-process and finished goods
• Record and maintain quality control documentation
• Support investigations into non-conforming products
• Support process audits for SOP and WI adherence
• Initiate Non-Conforming Events (NCEs)
• Review device history records and sales orders
• Participate in Kaizen and continuous improvement initiatives
• Complete training requirements and maintain records
• Regular, punctual attendance and ability to work overtime

Qualification & Experience:

• High school diploma or GED
• Ability to lift and move up to 40 pounds
• Prior manufacturing or quality experience appropriate for a Level II role
• Strong attention to detail
• Ability to follow SOPs and controlled documentation
• Reliability and consistent attendance
• Willingness and ability to work second shift
• 1-2 years preferred
• Quality or manufacturing experience
• Medical device industry experience
• GDP and GMP experience
• Experience in other regulated industries such as aerospace or pharmaceutical
• Basic Microsoft Office (Excel, Word, SharePoint, OneDrive)
• Ability to follow written procedures
• Effective written and verbal communication
• Teamwork and independent work capability
• High attention to detail
• Ability to read schematics and blueprints
• Familiarity with GMP and GDP
• Associate Degree preferred
• Familiarity with Oracle ERP or Agile PLM beneficial Working Conditions & Physical Demands (If Applicable):
• Sit, stand, walk, reach, stoop, kneel, crouch, crawl
• Lift/move up to 40 pounds
• Exposure to mechanical parts, vibration, moderate noise
• Safety shoes required in designated areas
• May work with high voltage electronics, radiation, clean rooms, controlled environments, or dark rooms Additional Information (If Applicable): PPE and Dress Code - Standard manufacturing and quality PPE as required on site.

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: $25.00/hr.