Job Description

TITLE : Quality Control Inspector II

LOCATION: Marlborough, MA

DURATION: 6 months + extension

INTERVIEW PROCESS: First round - 30-minute Teams interview / Second round - Onsite panel interview with tour.

MANAGER NOTES from Intake call – please pay attention to these –

• Perform inspections and reviews of raw goods.
• 3 month push on first article inspection completions for new product coming onboard Small close-knit team

Ability to adapt, flexibility

• Looking for actual inspectors , NOT warehouse/picker/receivers. Need a background in quality inspection rather than warehouse inspection.
• Day to day - Med device Manufacturing environment
• Performing inspections and supporting other inspectors Document review
• BG performing inspections in a regulated manufacturing environment is required (med device, auto, aerospace)
• Need General computer skills & Comfortable performing inspections

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.

Responsibilities :

The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.

• Support the receiving of incoming materials including offloading and organizing material, performing visual and dimensional inspections, and quantity verifications.

• Document the acceptability conditions of incoming materials in PLM (Product Lifecycle Management) system.

• Generate NCE’s for any non-conforming material identified during the inspection process.

• Identify and recommend disposition on nonconforming materials.

• Assure adequate and effective material status control at all times.

• Maintain and execute FIFO within work area. Move materials as required using standard material handling equipment. Release product in ERP system to released location.

• Maintain and promote a safe work environment at all times. Identify, address, and react to any unsafe or hazardous situation.

• 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.

Education

• High School or General Education Degree, May have Associate’s Degree

Experience

• 2-5 Years experience required

• Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial.

• Previous quality assurance or manufacturing experience is beneficial.

• Experience in FDA regulated medical device environment is beneficial.

Skills

• Ability to use Microsoft Office programs including Excel, Work, SharePoint and OneDrive, data entry and ERP systems.

• Ability to read, understand, and follow all written procedures. Ability to communicate effectively, both written and verbally. 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.

• Ability to operate material handling equipment.

• Familiarity with product specifications, blueprints and schematics is beneficial.

• Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) is beneficial.

Thanks!

Ritika Aithmian

Lead Recruiter

Ritika.aithmian@mastechdigital.com

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