Quality Systems Supervisor Position Available In Broward, Florida

Quality Systems Supervisor BioXtek LLC Pompano Beach, FL Job Details Full-time $70,000 – $80,000 a year 1 day ago Benefits Health insurance Dental insurance Paid time off Vision insurance Qualifications Six Sigma Certification 5 years Bachelor of Science Quality management

ISO 9001

Supervising experience Quality assurance Bachelor’s degree Continuous improvement Lean Six Sigma Quality systems Senior level Leadership Communication skills

ISO 13485 FDA

regulations Full Job Description Position Summary We are seeking a Quality Systems Supervisor to lead and manage critical elements of our Quality Management System (QMS). This role is responsible for ensuring the effective implementation, maintenance, and continuous improvement of quality systems that support GxP compliance, including document control, training, CAPA, deviation management, and audits. The ideal candidate will have strong knowledge of regulatory requirements (FDA, AATB, ISO), experience with electronic quality systems, and a hands-on leadership approach. Key Responsibilities Supervise and support day-to-day operations of core quality systems: Document control Training management Deviations and investigations CAPA Change control Internal/external audits Create and revise standard operating procedures and protocols. Investigate environmental monitoring quality events and determine primary root cause of organism introduction into the cleanrooms. Ensure timely closure of quality records in accordance with internal procedures and regulatory expectations. Partner with cross-functional departments (Manufacturing, QC, Regulatory) to drive quality initiatives and resolve compliance issues. Train, mentor, and develop QA associates supporting quality systems activities. Monitor QMS metrics and provide periodic reports to QA Management. Support inspection readiness and participate in regulatory inspections and audits. Contribute to continuous improvement initiatives to optimize quality system performance and compliance.

Qualifications Required:

Bachelor’s degree in life sciences, engineering, or related field. 5+ years of quality assurance experience in a GxP-regulated industry. 1-2 years in a leadership or supervisory role. Strong understanding of quality system elements under

FDA 21 CFR

Part 1271, 210/211, 820. Excellent technical writing, organizational, analytical, and interpersonal communication skills.

Preferred:

Knowledge of ISO 13485 and

ISO 9001.

Lean Six Sigma or continuous improvement certification a plus. Experience with electronic QMS platforms (e.g., Dot Compliance). Join our team as a Quality Assurance Manager where you can make a significant impact on product excellence and safety!

Job Type:

Full-time Pay:

$70,000.00 – $80,000.00 per year

Benefits:

Dental insurance Health insurance Paid time off Vision insurance

Schedule:

10 hour shift 8 hour shift Monday to

Friday Work Location:

In person