Document Control & Quality Data Coordinator

Bionostics, Inc.; Harvard (MA); On-site; USD 29,000 - 40,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401k with ESPP

HSAs and FSAs

Tuition reimbursement and training

Career development opportunities

Job summary

Bio-Techne in Massachusetts is seeking a detail-oriented Document Control/QA support associate to perform routine duties within the Document Management System, process and file documents, and assist multiple departments with document requests.

The role emphasizes accuracy, adherence to cGMP and GDP standards, strong computer skills, and the ability to manage competing priorities. Training and opportunities for growth are provided in a collaborative environment.

Qualifications

• Education and Experience: High school diploma with 3 years' experience in labeling/packaging operations in lieu of a diploma.
• Knowledge of cGMP requirements, GDP, and good documentation practices.
• Proficient computer skills and strong organizational abilities.

Responsibilities

• Complete basic tasks in the Document Management System (DMS).
• Upload and process documents, route within the DMS or databases.
• File and organize documents; maintain the shared data folder.
• Enter and verify lot information for OEM and Bionostics products.
• Configure and verify label files and barcodes for printing.
• Support continuous improvement of processes and standards.
• Perform all other duties as assigned.
• Adhere to safety guidelines and company policies.

Skills

Attention to detail

cGMP knowledge

GDP knowledge

Computer proficiency

Multitasking

Written and verbal communication

10-key typing

Electronic records

Interpersonal skills

Education

High school diploma

Job description

Bio-Techne in Massachusetts is seeking a detail-oriented Document Control/QA support associate to perform routine duties within the Document Management System, process and file documents, and assist multiple departments with document requests.

The role emphasizes accuracy, adherence to cGMP and GDP standards, strong computer skills, and the ability to manage competing priorities. Training and opportunities for growth are provided in a collaborative environment.