Detail-Driven Document Control Specialist

Bio-Techne; Massachusetts; On-site; USD 29,000 - 40,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Life and disability insurance

401k & ESPP plans

HSA / FSA options

Paid holidays and PTO

Job summary

Bio-Techne is seeking a detail-oriented Document Control/QA support specialist in Massachusetts. You will perform routine duties to maintain document control programs, upload documents in the DMS, and route files across departments to support manufacturing and purchasing.

Responsibilities include verifying lot information for OEM and Bionostics products, configuring label files and barcodes, and contributing to continuous improvement while adhering to GDP and cGMP requirements.

Qualifications

• High school diploma or 3 years labeling/packaging experience.
• Attention to detail with data review and basic calculations.
• Knowledge of cGMP, GDP, and quality systems.

Responsibilities

• Process documents in the DMS and upload packets.
• Route and organize documents across departments.
• Enter and verify lot information for OEM/Bionostics products.
• Configure and verify label files and barcodes for production.
• Support Continuous Improvement and maintain safety policies.
• Perform other duties as assigned.

Skills

Attention to detail

GDP knowledge

Time management

Written & verbal communication

Interpersonal skills

Typing (10-key)

Education

High school diploma

Tools

Document Management System (DMS)

Job description

Bio-Techne is seeking a detail-oriented Document Control/QA support specialist in Massachusetts. You will perform routine duties to maintain document control programs, upload documents in the DMS, and route files across departments to support manufacturing and purchasing.

Responsibilities include verifying lot information for OEM and Bionostics products, configuring label files and barcodes, and contributing to continuous improvement while adhering to GDP and cGMP requirements.