Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Quality Assurance Specialist

Job

GL Staffing

Boca Raton, FL (In Person)

$77,500 Salary, Full-Time

Posted 4 days ago (Updated 18 hours ago) • Actively hiring

Expires 7/9/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
61
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Quality Assurance Specialist at GL Staffing Quality Assurance Specialist at GL Staffing in Boca Raton, Florida Posted in about 20 hours ago.
Type:
full-time
Job Description:
Job description:
Job Title:
Quality Assurance (QA) Specialist - QMS / Investigations (Injectables)
Location:
Boca Raton Salary:
$70,000 - $80,000 per year
Experience Required:
Minimum 10 years
Industry:
Pharmaceutical / Biotech (Injectables)
Job Summary:
We are seeking an experienced Quality Assurance (QA) Specialist with strong expertise in Quality Management Systems (QMS) and pharmaceutical manufacturing, specifically within injectables. The ideal candidate will have extensive experience handling deviations, investigations, change control, and quality documentation while ensuring compliance with regulatory standards.
Key Responsibilities:
Manage and oversee Change Control processes to ensure compliance with internal procedures and regulatory requirements. Conduct and review compliant investigations, including OOS (Out of Specification) and OOT (Out of Trend) events. Review and support quality investigations related to manufacturing and laboratory activities. Maintain and review material specifications, SOPs, and batch documentation. Perform batch record review and batch release activities. Ensure adherence to GMP regulations and company Quality Management System (QMS). Collaborate with cross-functional teams including Manufacturing, QC, and Regulatory Affairs. Support audits and regulatory inspections as needed.
Qualifications:
Minimum 10 years of Quality Assurance experience in the pharmaceutical or biotech industry. Strong experience with injectable products. Proven expertise in QMS, Change Control, Deviations, OOS/OOT investigations. Experience reviewing SOPs, material specifications, and batch release documentation. Solid knowledge of GMP regulations and regulatory compliance. Strong analytical, documentation, and problem-solving skills. Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field preferred.
Compensation & Benefits:
Salary range: $70,000 - $85,000 Competitive benefits package Opportunity to work with a growing pharmaceutical organization