Formulation Technician II

Indotronix International Corporation•Plainville, MA
•Onsite

About The Position

The Formulation Technician II supports sterile pharmaceutical manufacturing operations in the Plainville, Massachusetts Drug Product organization. The role works in a highly regulated cGMP environment focused on quality, compliance, patient safety, and operational excellence. The technician performs all Band 1 responsibilities and independently executes sterile manufacturing operations, including formulation, filtration, and aseptic filling, applying technical expertise to support safe, compliant, and efficient production. The position routinely takes place in GMP manufacturing and controlled cleanroom environments. It requires use of personal protective equipment, gowning and working in classified manufacturing areas according to site procedures, and the ability to support operations during non-standard hours as business needs require. A color blindness test is required during the compliance check process.

Requirements

  • High school diploma or GED required.
  • At least 2 years of GMP manufacturing or related technical experience.
  • Working knowledge of GMP manufacturing operations.
  • Ability to operate and troubleshoot manufacturing equipment.
  • Strong documentation and problem-solving skills.
  • Ability to support multiple manufacturing processes.
  • Ability to communicate effectively in English, both written and verbal.
  • Ability to gown and work in classified manufacturing areas in accordance with site procedures.
  • Ability to lift up to 25 pounds occasionally.
  • Visual acuity sufficient to review documentation and perform quality inspections.
  • A color blindness test is required during the compliance check process.

Nice To Haves

  • Associate degree in a technical, scientific, or related discipline desired.
  • Relevant GMP manufacturing experience preferred.

Responsibilities

  • Perform all responsibilities of Formulation Technician I.
  • Execute material handling, line clearance, equipment preparation, and manufacturing support activities.
  • Execute sterile filtration, aseptic filling, and related manufacturing operations according to approved procedures.
  • Operate, monitor, and troubleshoot manufacturing equipment and automated systems.
  • Perform weight and dispense, solution preparation, autoclave operations, visual inspection, material transactions, and manufacturing support functions.
  • Ensure compliance with cGMP requirements, Good Documentation Practices, and data integrity standards.
  • Monitor manufacturing processes and identify opportunities to improve safety, quality, and efficiency.
  • Support investigations, deviations, change controls, and corrective actions as required.
  • Assist with equipment qualification, validation, and continuous improvement initiatives.
  • Cross-train across multiple manufacturing areas to support operational flexibility.
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