Quality Assurance Specialist Job Openings at ALS | Apply Now
Step into a rewarding role that merges precision, compliance, and scientific excellence. The Clinical Quality Assurance Specialist position at ALS is ideal for professionals seeking a meaningful impact in clinical research and quality systems. As one of the top Life Science Jobs among Jobs in USA, this opportunity empowers you to ensure data integrity, regulatory compliance, and high-quality clinical operations across a global organization.
About the Company
ALS is one of the worldโs largest providers of testing and technical services with operations in over 350 global locations. As an international leader supporting life sciences, pharmaceuticals, food, and minerals sectors, ALS offers competitive benefits, diverse work environments, and career development opportunities. Professionals joining ALS gain access to one of the most respected organizations offering Jobs in USA, especially for those pursuing careers as a quality assurance specialist.
Job Details:
- Job Title: Clinical Quality Assurance Specialist
- Location: Phoenix, AZ
- Schedule: Full-time, onsite, MondayโFriday, 8:00 a.m.โ5:00 p.m.
- Reports to: Quality Assurance Director
Position Summary
The Clinical Quality Assurance Specialist supports QA activities related to data review, report approval, controlled document management, and audit support within the Clinical Department. The role ensures studies comply with SOPs and Good Clinical Practice (GCP) guidelines and works closely with the QA Director and Clinical Director on routine and special projects.
Key Responsibilities of Quality Assurance Specialist
- Review raw data and clinical reports for accuracy and compliance.
- Perform final report review and QA release.
- Support management of the controlled document system (SOPs, protocols, forms, supporting documents).
- Maintain archives of completed notebooks, study files, and master documents; coordinate with external storage facilities as needed.
- Assist with onboarding/setup of new employees.
- Review and approve Deviations, CAPAs, and other quality-related requests.
- Assist with internal audits and follow-up on corrective actions.
- Ensure compliance with all Clinical Operations SOPs.
- Complete all tasks per current SOPs and GCP requirements.
- Support QA Management with special projects.
Qualifications
- Bachelorโs degree in a Life Science (Biology).
- Minimum 2 years of clinical or quality experience in an FDA-regulated industry.
- Experience with GMP and GCP.
- Strong reliability, quality focus, and attention to detail.
- Organized, responsible, and able to multitask effectively.
- Strong communication and technical writing skills.
Benefits of Quality Assurance Specialist Job
- Health Benefits: Medical, Dental, Vision
- Retirement: 401(k) and Roth with company match after 6 months
- Paid Time Off & Vacation
- Company-Paid Life Insurance
- Company-Paid Short- and Long-Term Disability
- Additional ancillary benefits.
