Quality Assurance Associate
Core
Perform in-process document auditing, final product release auditing, and finished product blister inspection to ensure compliance with cGMP and SOPs in pharmaceutical manufacturing.
Role type
Quality Assurance Associate (Manufacturing)
Builds
Pharmaceutical dosage forms (fast-dissolve oral dosage forms)
Domain
Pharmaceutical manufacturing / cGMP
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP knowledge, document auditing, deviation investigation, SOP writing/revising, batch release auditing, manual dexterity, close vision
Preferred skills
manufacturing experience, pharmaceutical/GMP facility experience, analytical problem-solving, coaching/leadership
Technologies
None stated
Responsibilities
Perform in-process document auditing and product quality checks; Conduct final release auditing of batch documentation; Assist in investigating manufacturing issues and deviations; Perform weekly compliance audits; Act as QA representative on shift for decision-making; Assist in writing and revising SOPs; Perform finished product blister inspection
Seniority
Entry-level, no previous experience required
