Formulation Technician II- Plainville MA 02762

Job Description

Job Description

Job Title: Formulation Technician II
Location: Plainville MA 02762
Duration: 12 Months
Pay rate: $30/hr.

Training will be Monday to Friday 7am 3:30pm (Roughly two to three months). After training the schedule will be 2-2-3 schedule. 2-2-3 starts at 7am and end at 7pm.

Job Description:

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.

Purpose:
Performs all Band 1 responsibilities and independently executes sterile manufacturing operations, including Formulation, Filtration, and Aseptic Filling. Applies technical expertise to support safe, compliant, and efficient production.

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 activities including 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.

Education :
Associate degree or Bachelor's degree in Life Sciences, Engineering, or a related field PREFERRED. Will consider applicants with experience in lieu of a degree.

Relevant GMP manufacturing experience preferred.

Experience:
2+ years GMP manufacturing or related technical experience.

Knowledge Skills, and Abilities:

·       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

Physical Environment:

·       Routine presence in GMP manufacturing and controlled cleanroom environments.

·       Required use of personal protective equipment (PPE).

·       Ability to gown and work in classified manufacturing areas in accordance with site procedures.

·       Frequent standing, walking, bending, and computer-based work.

·       Ability to lift up to 25 pounds occasionally.

·       Visual acuity sufficient to review documentation and perform quality inspections.

·       Ability to support operations during non-standard hours as business needs require.

·       Ability to communicate effectively in English, both written and verbal. (PPE).