Aseptic Manufacturing Technician

Trident Consulting; Indianapolis (IN); On-site; USD 37,000 - 41,000; Full time

Job summary

Trident Consulting is seeking a mid-level Aseptic Manufacturing Technician for a contract in Indianapolis, IN. The role centers on aseptic pharmaceutical manufacturing within a controlled cGMP/GMP cleanroom environment; isolator experience is preferred but not mandatory.

Responsibilities include aseptic filling, equipment setup, sanitization, and GMP documentation, with 1st shift, Monday–Friday, 7:00 AM–3:30 PM. Pay is $27–$30/hr W-2, with virtual or onsite interview options.

Qualifications

• 3–5 years of aseptic filling experience in a cGMP pharmaceutical facility.
• Hands-on experience with aseptic filling, equipment cleaning, preparation, and assembly.
• Strong knowledge of GMP/cGMP compliance and SOPs.

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 hazardous chemicals.
• Work with SIP100 and required PPE.

Skills

Aseptic filling

GMP/cGMP compliance

SOP documentation

Equipment cleaning

Batch records

Tools

SIP100

Job description

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 SIP100 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.