Quality Assurance Technician

Bio-Techne•Devens, MA
•$23 - $32

About The Position

The Quality Assurance Technician conducts periodic on-line inspections of assemblies and device history records, reviews final device history records, generates Certificates of Conformance, creates non-conformance records as applicable, reviews and releases in-house printed labels, and reports finished goods and retains in the ERP system. The role also supports customer-specific reports and programs and assists the documentation group as needed. Packaging QC duties include checking lot-specific labels, packaging materials, and printed information; inspecting labeling and packaging operations; performing finished-goods inspections using AQL standards; reviewing production and packaging documentation; maintaining product retains; and preparing Certificates of Conformance. The technician identifies and escalates quality issues, initiates Nonconforming Material Reports when required, and supports investigations, corrective actions, continuous improvement, UDI barcode verification, and OEM quality activities. Documentation support includes processing work order packets, generating and verifying lot assignment records, maintaining label files and specifications, supporting document control and production records, and recommending improvements to procedures and documentation. The technician follows company policies, SOPs, safety requirements, and cGMP regulations, and adapts to changing priorities while supporting team objectives.

Requirements

  • High school diploma.
  • Three years of experience in labeling and packaging operations.
  • Strong attention to detail and ability to accurately review data, perform basic calculations, and apply statistical sampling methods.
  • Knowledge of cGMP requirements, Quality Systems, and Good Documentation Practices (GDP).
  • Ability to ensure labeling, packaging, and documentation activities comply with quality standards and customer requirements.
  • Proficiency in computer applications, with strong organizational and time-management skills.
  • Ability to manage multiple priorities, meet deadlines, and adapt to changing schedules and business needs.
  • Effective written and verbal communication skills.
  • Efficiency with keyboard and 10-key typing.
  • Strong interpersonal skills and ability to collaborate effectively across all levels of the organization.

Responsibilities

  • Inspect and approve lot-specific labels, packaging materials, and printed information for accuracy and compliance.
  • Perform in-process inspections of labeling and packaging operations to verify product quality, component accuracy, and packaging requirements.
  • Conduct finished-goods inspections using AQL standards and support timely product release.
  • Review device history records, packaging documentation, and production records for completeness and accuracy.
  • Collect and maintain product retains and prepare Certificates of Conformance (COCs).
  • Identify, document, and escalate quality issues; initiate Nonconforming Material Reports (NCMRs) as required.
  • Support investigations, corrective actions (CAPA), and continuous improvement activities.
  • Perform UDI barcode verification and OEM-specific quality support activities, including customer sample submissions.
  • Process and maintain work order packets to support manufacturing operations.
  • Generate, enter, and verify lot assignment records (LAR/eLAR) and related product information.
  • Configure, verify, and maintain label files, barcodes, and imprinting specifications using approved software systems.
  • Ensure documentation is accurate, complete, and compliant with record management requirements.
  • Support document control activities, including Certificates of Analysis (COAs), Certificates of Conformance (COCs), infocards, and document packet updates.
  • Distribute and maintain production and labeling records as required.
  • Review procedures and recommend process, system, and documentation improvements.
  • Adhere to company policies, SOPs, safety requirements, and cGMP regulations.
  • Adapt to changing business priorities, manage workload effectively, and support team objectives.
  • Perform additional duties and projects as assigned.

Benefits

  • Competitive insurance benefits starting on day one, including medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield coverage.
  • 401(k) plans.
  • Employee stock purchase plan (ESPP).
  • Health Savings Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • Mentorship, promotional opportunities, training and development, tuition reimbursement, and internship programs.
  • Employee resource groups, paid volunteer time off, employee events, and charity drives.
  • Accrued leave policy with paid holidays, paid time off, and paid parental leave.
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