Quality Associate (Biotech/Pharma)

Job Description

As a Quality Associate, you will ensure data is accurately reviewed, scanned from physical records and tracked. Your contributions will support data reviews, data retention, and inspection readiness. This is an entry level 6-month contract with on-site office hours. This contract may be extended to a part-time position. This role will report to Vice President, Quality.

What you'll do

Conduct GMP reviews of test records, logbooks, and manufacturing records.

Organize, scan, and accurately track documents.

Ensuring all scanned documents are complete, and accurate.

Prepare spreadsheets, and other administrative materials as needed.

Assist in analytical sample inventory tracking

Qualifications

College degree (preferably in Biology, chemistry or equivalent.)

1-3 years’ previous experience in a pharmaceutical or related industry, particularly in GMP record review.

Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices)

Skilled in organization, communication, record-keeping, and attention to detail.

Ability to work independently and in a team.

Commitment to quality of work,

Proficient in Word and Excel.Company Description

The Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire & Contract Consultants) and Retained Executive Search.