Aseptic Manufacturing Technician

Trident Consulting; Indianapolis (IN); Vor Ort; USD 25.000 - 34.000; Vollzeit

Zusammenfassung

Trident Consulting is seeking a Production Technician II for a role in Indianapolis, IN. The position is 100% onsite with a pay rate of $21.50/hr W2 and a Monday–Friday shift from 7:00 AM to 3:30 PM, with overtime potential.

The role focuses on aseptic pharmaceutical manufacturing, cGMP compliance, packaging, vial washing, capping, and product inspection. Strong attention to detail and ability to lift up to 50 lbs are required.

Qualifikationen

• Aseptic manufacturing experience in a cGMP facility.
• Working knowledge of GMP regulations and SOPs.
• Ability to lift up to 50 lbs and work onsite.

Aufgaben

• Perform vial washing, capping, component preparation, packaging, and inspections.
• Set up equipment and replenish production supplies.
• Follow batch records, SOPs, and cGMP requirements.
• Verify scale calibration and inspect products for quality.
• Handle and dispose of hazardous chemicals safely.
• Operate production equipment with minimal supervision.

Kenntnisse

Aseptic manufacturing experience

GMP knowledge

SOP adherence

Attention to detail

Communication skills

Ausbildung

High school diploma or equivalent

Jobbeschreibung

Trident Consulting is seeking a " Production Technician II" for one of our clients in "Indianapolis, IN” a global leader in business and technology services.

Location: Indianapolis, IN 46268

Pay Rate: $21.50/hr w2

Shift: Monday–Friday, 7:00 AM–3:30 PM (Overtime possible)

Work Mode: 100% Onsite

Job Summary

Seeking a Production Technician II with experience in aseptic pharmaceutical manufacturing, cGMP compliance, packaging, and product inspection. Vial washing and capping experience are preferred.

Key Responsibilities

• Perform vial washing, capping, component preparation, packaging, and inspections.
• Set up equipment and replenish production supplies.
• Follow batch records, SOPs, and cGMP requirements.
• Verify scale calibration and inspect products for quality.
• Handle and dispose of hazardous chemicals safely.
• Operate production equipment with minimal supervision.

Required Qualifications

• High school diploma or equivalent.
• 2+ years of aseptic manufacturing experience in a cGMP pharmaceutical facility.
• Working knowledge of GMP regulations and SOPs.
• Strong communication and attention to detail.
• Ability to lift up to 50 lbs and work onsite.

Preferred: Vial washing, capping, packaging, inspection, and Microsoft Word/Excel experience.