Quality Assurance Associate, Pharmaceutical Manufacturing

Job overview

The Quality Assurance Associate works onsite in Winchester, KY; compensation is not specified. The role contributes to the production of high-quality pharmaceutical products. The associate supports manufacturing quality and compliance by reviewing batch records, monitoring production areas, conducting testing and environmental monitoring, and helping investigate deviations and complaints. The work helps maintain site compliance with standard operating procedures, current good manufacturing practices, and safety requirements.

What you'll do

• Recommend and review SOP and batch record changes
• audit batch records for accuracy and compliance
• perform room and equipment clearances and microbial swabbing
• test in-process and finished-product samples
• monitor production areas for SOP, cGMP, and safety compliance
• manage deviation reports and material quality status
• support investigations and process improvements
• train and coach manufacturing staff.

What we're looking for

Skills & competencies

quality assurance associate

pharmaceutical manufacturing

quality assurance

batch records

cgmp

sop compliance

trackwise

environmental monitoring

winchester ky

onsite

quality testing

Work arrangement

• Weekend coverage required

Why this role

Education may be a bachelor’s degree, an associate’s degree with one year of related experience, or a high school diploma/GED with two years of related experience. Temporary-to-permanent transition may be possible after six months.

About the employer

Abacus Service Corporation is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.