First-Shift Manufacturing Operations Supervisor (ILP)

QuVa Pharma; Sugar Land (TX); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health benefits

401k retirement plan

Paid time off - 22 days + 8 holidays

Job summary

Quva Pharma is seeking a Supervisor, Manufacturing Operations (ILP) for Sugar Land, TX. This full-time role on 1st shift (6:00 AM–2:30 PM) will coordinate daily operations across Inspection, Labeling, and Packaging and Label Printing.

The position emphasizes cGMP adherence, safety, and quality to ensure compliant production. You will supervise a team, manage schedules, track performance metrics, and support regulatory inspections while fostering cross-functional collaboration and continuous

Qualifications

• High school Diploma or GED required.
• 2–3 years in cGMP/FDA regulated industry.
• 1 year of supervisory/management experience.
• Understanding of CGMP, quality requirements and problem solving.
• Color and vision exams may be required for applicants.

Responsibilities

• Supervise staff in daily work and ensure SOPs, cGMP, and safety requirements are met.
• Oversee label printing activities and ILP scheduling.
• Prepare and submit production and metrics reports; identify continuous improvement opportunities.
• Maintain cross-functional relationships with Quality and other manufacturing operations teams.
• Lead in maintaining a safe manufacturing environment and ensure regulatory compliance.

Skills

Technical writing

Supervisory experience

Process improvement

Time management

Regulatory familiarity

Computerized tracking tools

Adult learning techniques

Education

High school diploma or GED

Bachelor's degree in Life Science or related field

Tools

Computerized tracking tools

Job description

Quva Pharma is seeking a Supervisor, Manufacturing Operations (ILP) for Sugar Land, TX. This full-time role on 1st shift (6:00 AM–2:30 PM) will coordinate daily operations across Inspection, Labeling, and Packaging and Label Printing.

The position emphasizes cGMP adherence, safety, and quality to ensure compliant production. You will supervise a team, manage schedules, track performance metrics, and support regulatory inspections while fostering cross-functional collaboration and continuous