ILP Production Technician I (1st Shift)

Quva-Pharma; Bloomsbury (NJ); On-site; USD 25,000 - 29,000; Full time

Benefits offered by this job

Health insurance

401k with company match

Paid time off

Overtime opportunities with notice

Career advancement opportunities

Job summary

Quva Pharma in Bloomsbury, NJ is hiring a Production Technician I – ILP to support visual inspection, labeling, and packaging at our site in Bloomsbury. You will follow established processes to ensure product safety, quality, and regulatory compliance.

This is a full‑time 1st shift role (Wednesday–Saturday, 4:30 AM–3:00 PM) on site. The position emphasizes accuracy, GDPs, cGMPs, and ISO standards; opportunities exist for growth and adherence to strict quality controls.

Qualifications

• High school diploma or GED required.
• Must pass color and vision exams and background check.
• Authorized to work in the United States on a full‑time basis; no visa sponsorship.
• Experience with cGMPs, GDPs, and ISO standards is preferred.

Responsibilities

• Assist preparation of inspection and packaging materials.
• Labeling and processing of production materials.
• Daily/bi-weekly/monthly cleaning and preventive maintenance documentation.
• Complete line and room clearances and accountability records.
• Document activities per established procedures; notify management of deviations.
• Assist with other areas as needed (cleaning, non-sterile filling, kitting).
• Labeling of products and final packaging; perform visual inspection.
• Support audits and maintain inspection-ready environment.

Skills

Attention to detail

Communication

Regulatory compliance

Quality assurance

Education

High school Diploma or GED

Job description

Quva Pharma in Bloomsbury, NJ is hiring a Production Technician I – ILP to support visual inspection, labeling, and packaging at our site in Bloomsbury. You will follow established processes to ensure product safety, quality, and regulatory compliance.

This is a full‑time 1st shift role (Wednesday–Saturday, 4:30 AM–3:00 PM) on site. The position emphasizes accuracy, GDPs, cGMPs, and ISO standards; opportunities exist for growth and adherence to strict quality controls.