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Quality Inspector

avantorsciences.com Logo

Avantor

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Location:
United States , Devens

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Category:
Quality Control

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Contract Type:
Not provided

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Salary:

45500.00 - 79500.00 USD / Year
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Job Description:

Avantor is looking for a Quality Inspector to ensure quality standards are met in a biopharma production environment. This role will be a full-time position based out of our Devens, MA office. Work Schedule: Monday-Friday, 7:30am-4:00pm.

Job Responsibility:

  • Perform Quality Inspection on incoming raw material components from suppliers
  • Evaluate all incoming documentation (packing list, Certificates of Conformance, Calibration Certificates, etc.) for compliance
  • Perform inspection disposition into ERP system
  • Follow AQL sampling plan
  • Comply with company policies, procedures, work instructions, and training requirements focusing on customer service, production, and quality
  • Ensure documentation and physical product segregation and containment of non-conforming material
  • Review production documentation for accuracy, completeness, and GDP compliance
  • Communicate issues / concerns to area owner and direct manager
  • Ensure that the area is in a state of “audit readiness” at all times
  • Perform inspection tasks by following established work instructions and procedures, by using required tools and methods and, when applicable, equipment, to determine acceptability of product, components and required documentation
  • Perform thorough inspections of raw materials, in-process samples, intermediate products, and final biopharmaceutical products to verify compliance with specifications and quality standards
  • Alert management when a non-conformance (NCM) is observed and follows appropriate NCM procedures
  • Document any deviations or non-conformances, following Avantor procedures and WI, encountered during inspections or routine activities
  • Ensure cleanliness of work areas
  • Perform other duties as assigned by Manager
  • Follow applicable safety procedures

Requirements:

  • High School completion or equivalent (GED) required
  • Minimum of 1 year related experience and/or training in a regulated industry is required
  • Experience in a Quality role within the medical device, biotech, or pharmaceutical industry is preferred
  • Good communication and interpersonal skills
  • Good attention to detail
  • Ability to read, understand, and follow procedures
  • Ability to escalate non-conforming material issues according to established procedures
  • Familiarity with QMS
  • GMP knowledge is preferred
  • Self-motivated and ability to work independently and with a team
  • Good mathematics skills
  • Knowledge of inspection tools and techniques

Nice to have:

  • Experience in a Quality role within the medical device, biotech, or pharmaceutical industry is preferred
  • GMP knowledge is preferred

Additional Information:

Job Posted:
January 15, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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