Quality Assurance Lead

15 hours ago

Tampa, Florida, United States SUN-PAC MANUFACTURING, INC. Full time
Job Overview

Position Summary: The Quality Control Supervisor is responsible for overseeing the quality assurance processes within the manufacturing environment, ensuring compliance with industry standards and internal protocols.

Key Responsibilities:

  • Conduct in-process evaluations of production methodologies and quality controls.
  • Accurately document findings in batch records while reviewing the visual processes of manufacturing personnel.
  • Verify that all components, raw materials, and in-process materials align with batch record specifications.
  • Execute line clearances and shift verifications to maintain a controlled processing environment.
  • Document and verify inspection outcomes as required in the batch records.
  • Perform visual and statistical sampling, ensuring compliance with approved specifications.
  • Manage the documentation for retains and storage of in-process materials and finished products.
  • Review batch production records for precision and thoroughness.
  • Conduct final compliance reviews and approvals of all batch documentation.
  • Identify and report non-conformances promptly.
  • Collect and retain samples for Quality Analysis in the laboratory.
  • Conduct swab tests and other assessments to ensure product compliance.
  • Ensure adherence to special instructions as necessary.
  • Document any quality issues accurately.
  • Identify and control any products with potential issues, managing quarantined items effectively.
  • Perform daily scale verifications and visual inspections of assigned areas for cleanliness and safety.
  • Ensure logbooks in all areas are completed and reviewed.
  • Provide On-the-Job Training (OJT) for quality processes as needed.
  • Collaborate closely with Quality Control Management to address deviations promptly, minimizing production downtime.
  • Enforce strict adherence to Good Manufacturing Practices (GMP), current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and regulatory standards.
  • Complete any additional duties as assigned.

Qualifications:

  • Education: Associate degree or equivalent experience.
  • Experience: 1-3 years in Quality Control within the pharmaceutical or dietary supplement industry preferred; 5+ years in a manufacturing/production setting.
  • Skills: Proficient in spreadsheet and word processing software (Excel and Word). Strong time management and communication skills are essential for effective interaction with production personnel and management.
  • Ability to perform calculations and utilize measuring instruments.
  • Excellent interpersonal skills and the ability to work collaboratively within a team.
  • Independent thinking and operational capability are required.
  • Language: Must be proficient in reading, writing, and speaking English; bilingual in English and Spanish is a plus.

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