Quality Assurance Specialist III

Job overview

The Quality Assurance Specialist III role is onsite in La Porte, TX. Compensation is not specified. AMPAC Fine Chemicals manufactures active pharmaceutical ingredients and registered intermediates for pharmaceutical customers. The role provides quality assurance support across programs and quality systems, helping ensure production and product release follow approved procedures. It coordinates QA input with cross-functional teams and customers and supports compliant, timely manufacturing and release activities.

What you'll do

• Communicate QA item status, including batch release and investigation status, to the IPT team
• provide guidance on approved systems and procedures for GMP production and release
• plan and execute production and product-release action items
• perform document control and production record reviews
• manage product releases and change controls
• review or conduct production and testing deviation investigations
• ensure validation and qualification requirements are documented in approved protocols and reports
• conduct facility audits at campaign start and periodically during long-running campaigns.

What we're looking for

Skills & competencies

quality assurance

pharmaceutical manufacturing

gmp

la porte tx

ampac fine chemicals

full-time

batch release

change control

deviation investigations

process validation

facility audits

production records

Work arrangement

• Weekend coverage required

Why this role

Supports multiple programs or coordination of quality systems; some guidance may be needed outside the typical working schedule. Typically requires 5–8 years of related experience with a bachelor's degree, or 3–6 years with a master's degree or equivalent experience.

About the employer

AMPAC Fine Chemicals is hiring for this role. Industry: Medicinal and Botanical Manufacturing. Sector: 32.