1st Shift Pharma Manufacturing Supervisor

RXinsider LTD.; Sugar Land (TX); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Health and wellness benefits

401k retirement program with company a

Paid time off

Job summary

Quva in Sugar Land, TX is seeking a Supervisor, Manufacturing Operations (ILP) to coordinate daily operations in Inspection, Labeling and Packaging and Label Printing. You will supervise staff, enforce SOPs and cGMP standards, and drive continuous improvement through data-driven metrics.

The role is full-time on first shift (Mon–Fri, 6:00 AM–2:30 PM) on site. Candidates should have prior supervisory experience in a 503B/pharma setting and be able to pass safety and vision tests.

Qualifications

• High school Diploma or GED required.
• 2-3 years prior experience in cGMP / FDA regulated industry.
• 1 year of supervisory or management experience required.
• Will be required to undergo color perception and vision exams.

Responsibilities

• Supervises staff in daily work; ensures SOPs, cGMP and safety compliance.
• Oversees label printing activities as needed.
• Manages ILP schedule per production plan and customer demand.
• Prepares daily/weekly/monthly reports and metrics for improvement.
• Maintains cross-functional relationships with Quality and other operations.
• Drives CAPA, Deviation, Change Control, and GMP tasks to close on time.
• Reviews batch records and logs for compliance and accuracy.
• Develops training programs and conducts training.

Skills

Supervisory experience

cGMP compliance

FDA regulated industry

Safety awareness

Education

High school Diploma or GED

Bachelor’s Degree in Life Science

Job description

Quva in Sugar Land, TX is seeking a Supervisor, Manufacturing Operations (ILP) to coordinate daily operations in Inspection, Labeling and Packaging and Label Printing. You will supervise staff, enforce SOPs and cGMP standards, and drive continuous improvement through data-driven metrics.

The role is full-time on first shift (Mon–Fri, 6:00 AM–2:30 PM) on site. Candidates should have prior supervisory experience in a 503B/pharma setting and be able to pass safety and vision tests.