Overview
Quality Assurance Specialist Jobs in Virginia, United States at Integrated Resources, Inc ( IRI )
Title: Quality Assurance Specialist
Company: Integrated Resources, Inc ( IRI )
Location: Virginia, United States
Job Title: Entry-Level Technical Specialist – Vaccine, Biologics, and Sterile Manufacturing Support
Location: Onsite
Shifts Available (Please specify availability):
First Shift: 8:00 AM – 5:00 PM
Second Shift: 2:30 PM – 10:30 PM (occasionally 8:00 AM – 5:00 PM)
Rotating 12-Hour Shift: 2:00 PM – 2:00 AM or 6:00 AM – 6:00 PM (7-day coverage)
Role Overview:
This role provides hands-on technical support in a cGMP-regulated vaccine and biologics manufacturing environment. The individual will be responsible for supporting floor operations, conducting investigations, and driving process improvement initiatives across both equipment and documentation. A blend of floor support (50%) and desk-based work (50%) is expected, with a strong emphasis on mechanical understanding and effective communication.
Key Responsibilities:
Provide technical troubleshooting and data analysis for sterile manufacturing processes
Conduct technical investigations and recommend/implement CAPAs
Support implementation of change controls and continuous improvement initiatives
Assist with writing, reviewing, and improving SOPs and operational procedures
Participate in equipment and process safety reviews
Perform on-shift support as required, including working alongside union operators, engineers, and maintenance staff
Maintain cGMP compliance and support reduction of atypical events
Required Qualifications & Skills:
B.S. or M.S. in Biology, Biochemistry, Biomedical/Chemical Engineering, Computer Science, Integrated Science, or related disciplines
0–3 years of relevant industry experience
No known Beta Lactam allergy (mandatory)
Excellent academic record and strong communication skills
Mechanically inclined with a hands-on approach to troubleshooting
Strong problem-solving ability with a field-first mindset
Ethical, self-driven, and a collaborative team player
Willingness to learn new systems and processes in a dynamic environment
Preferred Experience:
Internship, co-op, or work experience in a cGMP environment
Prior exposure to equipment operations, manufacturing floor support, and documentation (SOPs, reports)
