Document Control & Quality Assurance Coordinator

Bio-Techne; Harvard (MA); On-site; USD 29,000 - 40,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Long-term disability

401k plans

Employee stock purchase plan (ESPP)

Health Savings Account (HSA)

Job summary

Bio-Techne is seeking a detail-oriented Document Control/QA support role in Massachusetts. You will perform routine duties to maintain document control programs, manage documents in the DMS, and support multiple departments with scanning, filing, and uploading materials.

You will also verify lot information, configure label files and barcodes, and contribute to continuous improvement while following SOPs and safety guidelines. On-site work is expected with a collaborative team environment.

Qualifications

• Knowledge of cGMP requirements and GDP practices.
• Experience with document management systems and electronic records.
• Ability to manage multiple priorities and meet deadlines.
• Proficient in standard computer applications and data entry.

Responsibilities

• Complete basic tasks within the Document Management System (DMS).
• Upload documents and process packets.
• Route documents within the DMS and organize data.
• Maintain shared department data folders and scan/upload documents.
• Enter and verify lot information for OEM/Bionostics products.
• Configure and verify label files and barcodes for production printing.
• Contribute to continuous improvement of processes.
• Follow safety guidelines and company policies.

Skills

Attention to detail

GDP knowledge

Written and verbal communication

Time management

Electronic records experience

Interpersonal skills

10-key typing

Proficient with computers

Education

High school diploma

3 years' labeling/packaging operations experience in lieu of a diploma

Job description

Bio-Techne is seeking a detail-oriented Document Control/QA support role in Massachusetts. You will perform routine duties to maintain document control programs, manage documents in the DMS, and support multiple departments with scanning, filing, and uploading materials.

You will also verify lot information, configure label files and barcodes, and contribute to continuous improvement while following SOPs and safety guidelines. On-site work is expected with a collaborative team environment.