Technician, R&D Formulation

Role Overview

The Formulation Technician is responsible for supporting the formulation and manufacturing processes by accurately weighing, mixing, and processing raw materials in accordance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (cGMP), and batch documentation requirements. This role involves hands‑on operation and maintenance of various pharmaceutical production equipment and requires close adherence to quality, safety, and regulatory standards.

Date: 10/2025

Location:

1200 Airport Road, North Brunswick NJ

Title:

Technician, R&D Formulation

Department:
Research & Development

Reports to:

Director, Research & Development

FLSA (Exempt or Non-Exempt):
Non‑Exempt

The Formulation Technician is responsible for supporting the formulation and manufacturing processes by accurately weighing, mixing, and processing raw materials in accordance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (cGMP), and batch documentation requirements. This role involves hands‑on operation and maintenance of various pharmaceutical production equipment and requires close adherence to quality, safety, and regulatory standards.

Works under close supervision; learns formulation procedures, documentation, and equipment operation.

Works independently on complex formulation and scale‑up activities; may train junior staff.

Operates with minimal supervision; recognized technical expert and mentor within the R&D team. Develops and updates SOPs, batch records, and training materials. Oversees equipment readiness, preventive maintenance, and calibrations. Mentors technicians and ensures high‑quality documentation and compliance. Supports technology transfer and production readiness reviews.

• Accurately weigh and transfer raw materials using calibrated balances and scales in accordance with approved batch records and formulation guidelines.
• Perform formulation and manufacturing activities for pilot, scale‑up, and commercial batch production.
• Operate equipment for mixing, blending, granulation, and other material processing functions in support of pharmaceutical product development and manufacturing.
• Complete and maintain accurate, compliant, and timely documentation, including Batch Manufacturing Records (BMRs), Logbooks, Protocols, and related forms in accordance with cGMP and SOP requirements.
• Assist in the development and optimization of formulations for various dosage forms such as tablets, capsules, and granules, under the direction of senior formulation scientists or supervisors.
• Independently execute and monitor benchtop, pilot‑scale, and manufacturing scale‑up batches with minimal supervision.
• Set up, operate, clean, and perform changeovers on R&D and pilot‑scale manufacturing equipment, including but not limited to:
• Tablet Presses
• Capsule Filling Machines
• Coating Machines
• Granulators
• Fluid Bed Dryers (FBDs)
• Ensure equipment is properly maintained, sanitized, and operated in compliance with SOPs, safety protocols, and current Good Manufacturing Practices (cGMP).
• Proactively identify and troubleshoot issues during formulation development, demonstrating strong problem‑solving skills and an ability to anticipate potential risks or failures.
• Adhere strictly to all company policies, safety guidelines, and regulatory requirements.
• Participate in routine housekeeping, equipment cleaning, and 5S/continuous improvement initiatives to maintain a safe and efficient working environment.
• Perform additional duties and responsibilities as assigned by management to support departmental and organizational goals.