Quality Control Inspector Position Available In Pinellas, Florida
Tallo's Job Summary: The Quality Control Inspector position at SMP Nutra in Largo, FL involves monitoring product quality and ensuring compliance with FDA regulations and GMP standards. Responsibilities include inspections, testing, documentation, and collaboration with production teams. The role requires a high school diploma, 2 years of quality control experience, and proficiency in FDA regulations and measurement tools. The pay is $18.00 per hour with benefits and a Monday-Friday schedule.
Job Description
Quality Control Inspector SMP Nutra Largo, FL 33773
Job Title:
Quality Control (QC)
Inspector Position Summary:
The Quality Control (QC) Inspector is responsible for monitoring and ensuring that all products, materials, and processes comply with FDA regulations, GMP (Good Manufacturing Practices), and company quality standards in a dietary supplement manufacturing facility. This role conducts inspections, tests, and documentation reviews to ensure the production of safe, high-quality products. The QC Inspector works closely with production, packaging, and other teams to identify and address quality issues and maintain compliance.
Key Responsibilities:
Responsibilities include but are not limited to:
Product and Process Inspections:
Perform routine inspections of raw materials, in-process products, and finished goods to ensure compliance with specifications. Conduct visual and physical inspections on packaging components, including seals, labels, and overall integrity. Verify that manufacturing and packaging processes are conducted in accordance with approved batch records, work instructions, and GMP standards. Monitor production and packaging areas for adherence to cleanliness and hygiene standards.
Testing and Verification:
Utilize calibrated tools and equipment to perform measurements and tests, such as weight, dimensions, and other product-specific parameters. Verify proper setup and operation of manufacturing and packaging equipment before and during production. Conduct in-process checks at specified intervals to ensure consistency and quality.
Compliance and Documentation:
Review and verify accuracy and completeness of batch records, logbooks, and other production documentation. Record and report inspection findings accurately, identifying non-conformities or deviations promptly. Ensure compliance with FDA, GMP, and company standards during audits and inspections. Maintain accurate records of inspections, test results, and corrective actions in compliance with company policies.
Deviation and Non-Conformance Management:
Identify and document non-conforming products or processes and work with the Quality Assurance team to investigate and resolve issues. Assist in root cause analysis and recommend corrective and preventive actions (CAPAs). Quarantine and segregate non-conforming materials or products to prevent unintended use.
Collaboration and Communication:
Work closely with production and packaging teams to resolve quality issues in real-time. Provide feedback to operators and supervisors to ensure adherence to quality and safety protocols. Support quality training initiatives for production staff, as needed.
Continuous Improvement:
Participate in quality improvement projects aimed at enhancing product quality and process efficiency. Provide suggestions to improve inspection methods, testing protocols, and quality systems.
Qualifications:
Education and Experience:
High school diploma or equivalent required; Associate’s or Bachelor’s degree in a science-related field preferred. Minimum of 2 years of experience in a manufacturing quality control role, preferably in a GMP-regulated industry (dietary supplements, pharmaceuticals, or food manufacturing).
Skills and Abilities:
Strong knowledge of FDA regulations, GMP standards, and quality control principles. Proficiency in using inspection and measurement tools, such as calipers, scales, and micrometers. Excellent attention to detail with the ability to identify inconsistencies and deviations. Effective written and verbal communication skills for reporting findings and collaborating with cross-functional teams. Proficient in Microsoft 365 Office Suite (Word, Excel, Outlook) for documentation and reporting.
Physical Requirements:
Ability to stand, walk, and perform repetitive tasks for extended periods. Must be able to lift and move up to 30 pounds occasionally. Comfortable working in a manufacturing environment with varying temperatures and noise levels.
Core Competencies:
Attention to
Detail:
Ensures thorough and accurate inspection and documentation.
Analytical Thinking:
Identifies and resolves quality issues systematically.
Communication:
Clearly conveys findings and collaborates effectively with teams.
Adaptability:
Thrives in a dynamic, fast-paced manufacturing environment.
Compliance Focus:
Demonstrates a strong understanding of regulatory and company quality standards.
Pay:
$18.00 per hour
Hours:
Monday – Friday 7AM-3:30PM with a 30-minute lunch break
Benefits:
Paid Time Off Sick Time Paid Holidays Health Insurance 401(k) 1-4 Company Events per calendar year
Work Location:
Largo, FL (In-person) Ability to commute and/or relocate prior to starting work (Required).
Job Type:
Full-time Pay:
From $18.00 per hour
Benefits:
401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Life insurance Paid time off Vision insurance
Schedule:
8 hour shift Monday to
Friday Work Location:
In person