Quality Assurance Associate – Pfizerย
Pfizer is currently hiring a Quality Assurance Associate for its Bothell, Washington, facility. This full-time, on-premise role plays a vital part in ensuring the delivery of safe, compliant, and high-quality pharmaceutical products. If you are passionate about quality systems, documentation control, and supporting GMP operations, this QA Role at Pfizer Careers offers the opportunity to contribute directly to patient safety and global healthcare outcomes. Join for the QA Jobs.
Job Details:
- Position: Quality Assurance Associate
- Location: Bothell, Washington, United States
- Employment Type: Full Time
- Work Model: On-Premise
- Job Requisition ID: 4945952
- Posted: 2 Days Ago
- Salary Range: $66,500 โ $110,900 annually
- Bonus Eligibility: Yes (7.5% of base salary under Pfizerโs Global Performance Plan)
- Benefits: 401(k) with matching, Pfizer retirement contributions, paid leave (vacation, holidays, medical, parental), medical/dental/vision coverage, and more.
About the Company:
Pfizer is a global leader in pharmaceuticals, recognized for developing innovative medicines and vaccines that improve lives worldwide. The companyโs strong commitment to quality, scientific excellence, and risk-based compliance drives its mission to deliver safe and effective products to patients. Working at Pfizer means contributing directly to healthcare advancements and global patient well-being.
Educational Requirements for the QA Role:
You must meet one of the following:
- Bachelorโs degree in Life Science
- Associate degree + 3 years of relevant experience
- High school diploma or equivalent + 6 years of relevant experience
Preferred:
- Experience working at a pharmaceutical manufacturing site
- Experience in deviations, change control, CAPA, and batch record management
Key Responsibilities of the QA Role:
- Execute established procedures, work instructions, and templates
- Process documents in the electronic Document Management System
- Issue and reconcile batch records, logbooks, and forms
- Manage controlled documents and distribute them as required
- Support Records Management functions, including receiving, logging, cataloging, filing, and retrieving GMP records
- Work cross-functionally to improve GMP records systems and processes
- Support audits and inspections by ensuring timely record retrieval
- Scan and digitize GMP records and verify accuracy
- Collect and assist with reporting relevant system metrics
- Coordinate with off-site storage facilities for compliant record handling
- Participate in continuous improvement and process optimization initiatives
Skills Required for the QA Role:
Minimum Requirements:
- Knowledge of pharmaceutical industry quality systems
- Understanding of current Good Manufacturing Practices (cGMP/GxP)
- Strong communication skills (written and verbal)
- Ability to work effectively within and across teams
Preferred Skills:
- Batch record issuance and reconciliation
- Non-conformance investigation and root cause analysis
- Change control and CAPA management
- Strong problem-solving ability
- Time management and multitasking proficiency
- Ability to work independently
How to Apply for the QA Jobs?
To apply for this QA role, visit the official Pfizer careers portal. Ensure you have an updated resume and relevant experience documents ready. Applicants are encouraged to register on the site for job alerts and updates regarding similar opportunities.
