Key Responsibilities

A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully. Manufacturing Operations Execute manufacturing processes for drug products per approved procedures Request and dispense raw materials for production Operate production equipment including reactors, filters, dryers, formulation, milling, and filling systems Collect in-process samples for laboratory testing Clean and maintain equipment and production areas in accordance with cGMP standards Follow safety procedures and maintain a clean, hazard-free work environment Handle and manage production waste in compliance with safety and environmental regulations Documentation & Compliance Complete and review batch records in accordance with Good Documentation Practices (GDP) Maintain accurate and timely logbook entries Follow Standard Operating Procedures (SOPs) precisely Revise GMP documents as required Support deviation investigations and other GMP documentation activities Maintenance & Instrumentation Support Assist in preventative maintenance of equipment and instrumentation Support upkeep of equipment logs and calibration records Suggest and implement improvements to equipment or processes Monitor and record environmental conditions as required Maintain adequate inventory of production consumables and supplies

Qualifications Education High school diploma, GED, or equivalent required Bachelor’s degree in a scientific or technical field preferred Skills & Competencies Strong mechanical aptitude and problem-solving ability Excellent attention to detail and accuracy in documentation Proficient in basic mathematics and computer applications (MS Office Suite) Ability to follow complex written and verbal technical instructions Strong communication skills, both written and verbal Demonstrated ability to work in a team-based environment Experience 2–4 years of experience in a GMP-regulated manufacturing environment or equivalent Hands-on experience with operating, cleaning, and maintaining pharmaceutical production equipment Experience with SOPs, deviations, and validation protocols preferred Previous experience training other technicians is a plus