QA Operations Associate, GMP Manufacturing

Job overview

The QA Operations Associate, GMP Manufacturing role is onsite in Fort Lauderdale, FL. Compensation is not specified. The associate supports Goodwin Biotechnology’s manufacturing operations through on-floor quality assurance oversight. The role helps ensure manufacturing activities follow GMP requirements and aseptic practices by providing real-time quality review, supporting investigations, and escalating risks. This work contributes to compliant production records, inspection readiness, and controlled manufacturing operations.

What you'll do

• Provide real-time QA oversight in classified manufacturing areas
• conduct GMP walkthroughs
• serve as QA point of contact during manufacturing
• make independent GMP decisions and escalate or stop operations when required
• support deviation investigations
• review batch records, logbooks, and cleaning documentation
• support media fills, line clearances, and room/equipment release
• review SOPs, batch records, and specifications
• support audits and inspections
• coordinate record archiving
• support electronic environmental and NetSuite systems.

What we're looking for

Skills & competencies

qa operations associate

quality assurance

gmp

cgmp

aseptic manufacturing

batch records

deviation investigations

inspection readiness

biotechnology

fort lauderdale fl

goodwin biotechnology

Work arrangement

• Weekend coverage required

Why this role

The posting requires a high school diploma at minimum, knowledge of cGMP, aseptic manufacturing, and data integrity, and 1+ year of GMP experience. An associate or bachelor’s degree is preferred.

About the employer

Goodwin Biotechnology Inc is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.