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Aseptic Manufacturing Technician

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Trident Consulting
Full Time position
Listed on 2026-10-12
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Production Associate / Production Line
  • Pharmaceutical
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 27 - 30 USD Hourly USD 27.00 30.00 HOUR
Job Description & How to Apply Below
Location: Indianapolis

Trident Consulting is seeking a "Aseptic Manufacturing Technician" for one of our clients in "Indianapolis, IN" A global leader in business and technology services.

Location: Indianapolis, IN

Contract: 09/18/2026 – 09/17/2027

Schedule: 1st Shift, Monday–Friday, 7:00 AM–3:30 PM

Pay: $27–$30/hr w2

Interview: Virtual or Onsite

Position Overview

Mid-level role supporting aseptic pharmaceutical manufacturing in a controlled cGMP/GMP cleanroom environment
. Isolator experience is preferred but not mandatory
. Pharmaceutical manufacturing experience is required; food-industry experience does not qualify.

Key Responsibilities
  • Perform aseptic filling operations using SOPs and batch records
    .
  • Support cleanroom entry, sanitization, equipment setup, and supply replenishment.
  • Perform component preparation, filling, capping, and related manufacturing activities.
  • Operate and clean/prepare manufacturing equipment.
  • Verify equipment calibration and maintain GMP compliance.
  • Work independently with minimal supervision.
  • Train new team members and provide floor leadership when needed.
  • Follow safety procedures when handling/disposing of hazardous chemicals.
  • Work with SIP
    100
    and required PPE.
Required Qualifications
  • 3–5 years of relevant aseptic filling experience in a cGMP pharmaceutical manufacturing facility.
  • Strong knowledge of GMP/cGMP compliance
    .
  • Hands-on experience with aseptic filling, equipment cleaning, preparation, and assembly
    .
  • Stopper preparation, capping, and packaging experience preferred.
  • Ability to follow detailed SOPs and GMP documentation.
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