Specialist, Quality Systems & Compliance

Job Description

Must be able to work 12 hour night shift 6:00 pm to 6:00 am; 2-2-3 schedule.

Our Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored, and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

The Quality Assurance Associate Specialist provides Quality support to both laboratory and manufacturing operations. The successful candidate will have the opportunity to apply their enthusiasm and skills as a member of a multidisciplinary team supporting the operation of vaccine product manufacturing facilities. The successful candidate must be able to examine issues from various perspectives, provide a hands‑on approach to problem solving, and be self‑motivated to identify and initiate process improvement projects.

The Quality Assurance Specialist provides support to vaccine, biologic, and sterile manufacturing processes through collaboration with Technical Operations.

• Perform review of batch records, laboratory records and associated documentation.
• Provide quality guidance and assistance in deviation identification and initiation.
• Perform data review and run reconciliation activities as required (i.e., UV and FIT testing).
• Learn new processes and procedures.
• Perform shift work as required.
• Support housekeeping and self‑inspections.
• Perform Quality retain sample management activities, if applicable.

High School Diploma or equivalent.

• Minimum two (2) years' experience in Manufacturing, Maintenance, Military environments, or relative industry experience.
• Must be able to work 12 hour night shift 6:00 pm to 6:00 am; 2-2-3 schedule.

• Good interpersonal skills including flexibility and collaboration.
• Demonstrated analytical aptitude, critical thinking skills, and problem solving.
• Good verbal and written communication skills.

Analytical Problem Solving, Analytical Problem Solving, Aseptic Filling, cGMP Compliance, Communication, Complaint Management, Decision Making, Deviation Management, Global Manufacturing, Good Manufacturing Practices (GMP), Manufacturing, Oral Communications, Performance Improvement Plans, Problem Solving, Process Improvement Projects, Process Improvements, Quality Assurance (QA), Quality Auditing, Quality Management, Quality Management Standards, Quality Management Systems (QMS), Quality Standards, Quality Support, Root Cause Analysis (RCA), Sterile Procedures {+ 1 more}

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights, EEOC GINA Supplement, Learn more about your rights, including under California, Colorado and other US State Acts.

$71,900.00 - $

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at

07/4/2026