Pharma Production Tech I - Prep (1st Shift)

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

Benefits offered by this job

Set schedule

Health benefits

401k with match

Paid time off (PTO)

Overtime opportunities with notice

Career advancement

Job summary

Quva is seeking a Production Technician I – Prep in Bloomsbury, NJ for a full-time, 1st shift role (Mon–Fri, 6:00 AM–2:30 PM). You will support CSP manufacturing processes, cleanrooms, labeling, and GDP-compliant documentation, ensuring quality and safety in sterile pharmaceutical production.

The job requires a HS diploma, ability to lift 50 lbs, familiarity with mobile devices, and US work authorization. On-site position with potential overtime and safety-sensitive conditions.

Qualifications

• High school diploma or GED from a recognized institution.
• Able to successfully complete a background check.
• 18+ years of age.
• Able to walk, stoop, stand, bend, and lift up to 50 lbs. throughout shift.
• Familiarity with and comfortable using mobile devices.
• Authorized to work in the United States on a full-time basis; no visa sponsorship.

Responsibilities

• Support cleanrooms, formulations, ILP, and compounding.
• Assist in preparation, transportation, labeling, production, and processing of materials.
• Daily/weekly/monthly cleaning of rooms and equipment while adhering to standards.
• Maintain aseptic gowning qualified to support cleaning.
• Complete necessary documents for accountability and traceability of product following GDPs.
• Manage FEFO of chemicals, pulling expired ones monthly.
• Complete documentation of activities in accordance with established procedures.
• Perform sterile filter integrity testing as required.

Skills

Active listening

Team collaboration

Customer oriented

Initiative

Education

High School Diploma or GED

Job description

Quva is seeking a Production Technician I – Prep in Bloomsbury, NJ for a full-time, 1st shift role (Mon–Fri, 6:00 AM–2:30 PM). You will support CSP manufacturing processes, cleanrooms, labeling, and GDP-compliant documentation, ensuring quality and safety in sterile pharmaceutical production.

The job requires a HS diploma, ability to lift 50 lbs, familiarity with mobile devices, and US work authorization. On-site position with potential overtime and safety-sensitive conditions.