Quality Supervisor – GMP/FDA Manufacturing

About the role

We’re partnering with a manufacturer in Howell Township that’s hiring a Quality Control Supervisor to lead daily QC operations on the production floor. This is a hands-on role for someone coming from a GMP/FDA-regulated environment who can train teams, tighten processes, and drive quality results.

Responsibilities

• Train and coach QC Inspectors and plant operators on inspection procedures and quality expectations
• Ensure inspection coverage across production lines and daily operations
• Maintain training records and support SOP/GMP/GDP training
• Review batch records quickly and accurately to ensure compliance
• Manage the hold/release process and communicate status to site leadership
• Support customer complaint investigations with required quality data
• Maintain sample flow to the Quality Lab and support OOS investigations
• Maintain retain samples and related documentation
• Escalate defects to management and enforce SOPs/GMP standards
• Lead and develop the QC team while reducing defects and customer complaints

Requirements

• 2+ years in a GMP and/or FDA-regulated manufacturing environment
• Prior leadership/lead experience (supervising, training, or owning QC execution)
• Strong attention to detail and comfort enforcing standards on the floor
• Experience with batch record review and documentation compliance
• Proficiency in Microsoft Office; ERP experience is a plus
• Bachelor’s degree in Food Science or related field preferred (not required with strong experience)
• Familiarity with regulated standards is a plus (ex: 21 CFR 111, HACCP)

Qualifications

• Not specified

Skills

• Not specified

Benefits

• Not specified

Pay

$100,000–$110,000 salary

Schedule

100% Onsite | Mon–Thurs | 5:00 AM – 3:30 PM (1st Shift)