Formulation Technician II
About The Position
The Plainville, MA Drug Product organization supports sterile pharmaceutical manufacturing operations, including visual inspection, formulation support, aseptic processing, and related GMP activities. Colleagues work in a highly regulated cGMP environment focused on quality, compliance, patient safety, and operational excellence. The Formulation Technician II performs all Band 1 responsibilities and independently executes sterile manufacturing operations, including Formulation, Filtration, and Aseptic Filling. The role applies technical expertise to support safe, compliant, and efficient production.
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 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.
- Ability to communicate effectively in English, both written and verbal.
Nice To Haves
- Associate degree in a technical, scientific, or related discipline.
- Relevant GMP manufacturing experience.
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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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
