QA In-Process Specialist - Sterile 503B Manufacturing

Aveva Drug Delivery Systems; Florida; On-site; USD 50,000 - 60,000; Full time

Job summary

Aveva Drug Delivery Systems in Tamarac, FL seeks a Quality Assurance In-Process (QAIP) specialist to support upcoming 503B operations. The role focuses on real-time quality oversight of aseptic manufacturing and continuous process improvements.

You will work closely with Manufacturing to maintain cGMP compliance, review batch records, perform in-process inspections, and assist with deviation investigations and environmental controls. Strong collaboration and attention to detail are essential.

Qualifications

• B.A. or B.S. degree with 1–3 years related experience in pharma manufacturing.
• Strong knowledge of cGMP regulations and quality systems.
• Experience with aseptic processing, documentation, and QA walkthroughs.
• Proficiency in MS Office (Word, Excel, PowerPoint, Outlook).
• Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

• Provide dedicated QA oversight for 503B operations and aseptic processing.
• Perform in-process inspections and review batch records in real time.
• Collaborate with Manufacturing to ensure cGMP compliance and immediate quality assessments.
• Support deviation investigations and environmental/cleanroom monitoring.

Skills

cGMP knowledge

Quality systems

Aseptic processing

Documentation

MS Office

Interpersonal collaboration

Procedural interpretation

Education

B.A./B.S. degree

Job description

Aveva Drug Delivery Systems in Tamarac, FL seeks a Quality Assurance In-Process (QAIP) specialist to support upcoming 503B operations. The role focuses on real-time quality oversight of aseptic manufacturing and continuous process improvements.

You will work closely with Manufacturing to maintain cGMP compliance, review batch records, perform in-process inspections, and assist with deviation investigations and environmental controls. Strong collaboration and attention to detail are essential.