Find & Apply For Quality Control Analyst Jobs in Fort Lauderdale, Florida

Job Requirements:

• Ability to perform visual and dimensional inspections on components and finished products
• Ability to read and interpret blueprints, engineering drawings, and inspection instructions
• Basic understanding of quality control and inspection processes
• Ability to use precision measuring instruments (calipers, micrometers, gauges, rulers, etc.)
• Strong attention to detail and commitment to product quality
• Basic computer skills with the ability to enter and maintain inspection records
• Ability to perform ERP system transactions related to inspections and product release
• Ability to review and maintain accurate quality documentation
• Ability to identify, document, and segregate nonconforming materials
• Ability to follow Standard Operating Procedures (SOPs) and work instructions
• Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) preferred
• Ability to perform First Article Inspections (FAI) and verify inspection results is a plus
• Strong organizational, analytical, and problem-solving skills
• Effective verbal and written communication skills
• Ability to work independently and as part of a team
• Ability to meet quality, productivity, and safety goals in a fast-paced manufacturing environment
• Experience working in a regulated industry (medical device, pharmaceutical, aerospace, or electronics) preferred
• Ability to maintain accurate records and support compliance with regulatory requirements
• Flexibility to support changing production priorities and business needs

Job Summary:

• Perform visual, dimensional, and functional inspections of medical device components, subassemblies, and finished products.
• Ensure products meet quality standards, engineering specifications, and regulatory requirements.
• Inspect parts using blueprints, drawings, inspection guides, and precision measuring equipment.
• Conduct incoming, in-process, and final inspections to verify product conformity.
• Perform First Article Inspections (FAI) and verify inspection data when required.
• Review Device History Records (DHRs) and quality documentation for accuracy and compliance.
• Process inspection results, product release activities, and quality transactions within the ERP system.
• Identify, document, and quarantine nonconforming materials while initiating nonconformance reports as needed.
• Maintain compliance with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and company quality procedures.
• Support departmental quality, productivity, and Key Performance Indicator (KPI) goals.
• Maintain accurate inspection records and documentation to ensure product traceability.
• Work collaboratively with Manufacturing, Engineering, and Quality teams to resolve quality issues and support continuous improvement initiatives.
• Follow established procedures and work instructions while maintaining a safe and organized work environment.
• This is an entry-level opportunity with training provided for candidates looking to build a career in Quality Assurance and Medical Device Manufacturing.
• Only those lawfully authorized to work in the designated country associated with the position will be considered.
• Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.