Technician, R&D Formulation

Areas of Responsibility

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
• 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.

• 1 to 4 years of experience working in a nutraceutical/pharmaceutical, biotech, or food manufacturing environment, regulated by GMP standards and requirements.
• Specific experience in oral solid dosage manufacturing, blending, compression, pan coating, fluid bed, or encapsulation manufacturing processes will be a plus.
• 6 to 10 years’ experience working in a nutraceutical/pharmaceutical, biotech, or food manufacturing environment, regulated by GMP standards and requirements.
• Specific experience in oral solid dosage manufacturing, blending, compression, pan coating, fluid bed, or encapsulation manufacturing processes.
• Associate’s or Bachelor’s degree in Chemistry, Biology, Engineering, or related scientific field.
• 3 to 12 years’ experience working in a nutraceutical/pharmaceutical, biotech, or food manufacturing environment, regulated by GMP standards and requirements.
• Specific experience in oral solid dosage manufacturing, blending, compression, pan coating, fluid bed, or encapsulation manufacturing processes.

• N/A

• Requires hands‑on experience or knowledge to set‑up & operate Tablet, Capsule, Granulation manufacturing process equipment such as Tablet Press, Capsule Filling, Coating, Granulator, Fluid Bed Dryers, etc. and the ability to troubleshoot this equipment.
• Utilizes problem‑solving skills to investigate and troubleshoot product issues and recommend solutions for issues such as sticking, picking, capping, chipping, compressibility, delamination, etc.
• Works independently or in a team assisting others.
• Performs basic math calculations and follows written instructions with accuracy and pays attention to detail.
• Able to follow and understand cGMP, OSHA standards,…