×
Register Here to Apply for Jobs or Post Jobs. X

Quality Control Manager - Manufacturing​/Dietary Supplements

Job in Tampa, Hillsborough County, Florida, 33602, USA
Listing for: Express Employment Professionals
Full Time position
Listed on 2026-09-03
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Production QC/QA
Salary/Wage Range or Industry Benchmark: 72800 USD Yearly USD 72800.00 YEAR
Job Description & How to Apply Below

Quality Control Manager - Manufacturing/Dietary Supplements

Location:

Tampa, FL 33634

Schedule:

M-F 7:30am-4pm

Pay: $72,800 annual salary, $35/HR

General Purpose

The QA Manager is responsible for ensuring the quality of in-process and finished products, overseeing documentation, data integrity, label control, and maintaining substantial compliance with cGMP (21 CFR Part 111).

Key Responsibilities
  • Manage QC personnel performing verification, inspection, and testing of materials, products, packaging, and labeling
  • Oversee quality processes including specifications, forms, label control, batch record issuance, and equipment records
  • Review, approve, and release batch records
  • Maintain and improve quality systems; collect and analyze quality data
  • Manage calibration programs and coordinate activities with external labs
  • Audit laboratory results and maintain Certificates of Analysis
  • Communicate essential quality information across departments
  • Support production and shipping timelines through cross-department collaboration
  • Coordinate reserve sample storage
  • Prepare, revise, review, and approve SOPs and controlled documents
  • Conduct training as needed
  • Perform all other duties assigned by management
Minimum Qualifications Education
  • Bachelor's degree in Engineering, Life Sciences, or related field (or equivalent experience)
Experience
  • 5+ years in a cGMP environment (Dietary Supplements, Drugs, Cosmetics, or Medical Devices)
  • 3+ years of supervisory experience
Knowledge, Skills & Abilities
  • Strong understanding of cGMP, 21 CFR 111, SOPs, and Batch Records
  • Knowledge of 21 CFR 210/211 preferred
  • Team leadership and development skills
  • Proficient in Word, Excel, PowerPoint, Outlook
  • Strong writing, proofreading, and communication skills
  • Detail-oriented with strong interpersonal skills
  • Quality system management knowledge
Certifications
  • ASQ certifications (CQE, CQA, etc.) preferred
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary