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Bio-Techne

Purified proteins and reagents supplier

Quality Assurance Technician

Inspection & Test +1Confirmed live in the last 24 hours
Full-timeDevens, MA, USA$23.20 - $31.90In-person

About the Job

Requirements

  • A high school diploma is required.
  • Three years of experience in labeling and packaging operations is required.
  • Demonstrate strong attention to detail; accurately review data, perform basic calculations, and apply statistical sampling methods.
  • Have knowledge of current Good Manufacturing Practice (cGMP) requirements, Quality Systems, and Good Documentation Practices (GDP).
  • Ensure labeling, packaging, and documentation activities comply with quality standards and customer requirements.
  • Be proficient in computer applications and demonstrate organizational and time management skills.
  • Manage multiple priorities, meet deadlines, and adapt to changing schedules and business needs.
  • Communicate effectively in writing and verbally.
  • Type efficiently using a keyboard and 10-key keypad.
  • Collaborate effectively across all levels of the organization.
  • Work authorization must not now or in the future require visa sponsorship in the United States.

Responsibilities

  • Conduct periodic on-line in-process inspections of assemblies and device history records, final device history-record reviews, Certificate of Conformance generation, non-conformance generation as applicable, review and releasing of in-house printed labels, and ERP reporting of finished goods and retains.
  • Support customer-specific reports and programs and assist the documentation group as required.
  • 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, standard operating procedures (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.

About the Company

Bio-Techne

Purified proteins and reagents supplier

Bio-Techne develops and manufactures life-science products such as purified proteins, cytokines, antibodies, immunoassays, and reagent solutions. It serves academic labs, biotechnology firms, and pharmaceutical companies, and markets ProteinSimple-branded protein analysis tools along with cell and gene therapy workflow technologies. The company differentiates itself by offering a broad, integrated portfolio that spans from raw biomolecules to analytical solutions, enabling end-to-end research support. Its goal is to be a leading provider of life-science tools that accelerate discovery and development in life sciences and healthcare.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Minneapolis, MN
Founded
1981

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