1st Shift Manufacturing Operations Supervisor – Quality Leader

Quva; Sugar Land (TX); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Health, dental, vision

401k with company match

Paid time off

Career advancement opportunities

Stable full-time schedule

Job summary

Quva is seeking a Supervisor, Manufacturing Operations (ILP) in Sugar Land, TX for a 1st shift (Mon–Fri, 6:00 AM–2:30 PM). You will supervise staff across Inspection, Labeling, Packaging, and Label Printing operations, ensuring strict adherence to cGMP and safety standards to deliver high-quality, compliant products for patients.

The role emphasizes regulatory readiness, continuous improvement, and personnel development.

Qualifications

• Minimum requirements include a high school diploma or GED.
• 2-3 years of prior experience in a cGMP/FDA regulated environment.
• 1 year of supervisory or management experience required.
• Awareness of CGMPs and quality requirements in 503B pharmaceutical settings.

Responsibilities

• Supervise staff in daily work and ensure SOP, cGMP, and safety compliance.
• Oversee label printing activities and production scheduling.
• Prepare and review daily/weekly/monthly reports and metrics.
• Maintain cooperative cross-functional relationships with Quality and other operations.
• Lead safety initiatives and maintain a safe manufacturing environment.
• Assist in training front line leaders and developing career paths.
• Support regulatory inspections (DEA/FDA) as needed.
• Drive CAPA, deviations, and change control tasks to closure.
• Review batch records and logs for accuracy and compliance.

Skills

cGMP

Supervisory

FDA regs

Education

High school Diploma

Bachelor’s Degree in Life Science

Job description

Quva is seeking a Supervisor, Manufacturing Operations (ILP) in Sugar Land, TX for a 1st shift (Mon–Fri, 6:00 AM–2:30 PM). You will supervise staff across Inspection, Labeling, Packaging, and Label Printing operations, ensuring strict adherence to cGMP and safety standards to deliver high-quality, compliant products for patients.

The role emphasizes regulatory readiness, continuous improvement, and personnel development.