Production Technician I
STAQ Pharma
Software Engineering, Product
Columbus, OH, USA
Posted on Mar 11, 2025
| This position functions primarily in a controlled-non-classified (CNC) environment and requires the individual to wear appropriate PPE. This position will perform labeling, visual inspection, and other duties, such as cleaning, restocking, and waste destruction, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required. Hours of Work: 8-hour shift Monday through Friday |
| SAFETY Strictly adhere to all cGMP, health and safety requirements, procedures, and corporate policies.Authorized to immediately stop any task that is determined to be an imminent hazard.Always promote and demonstrate safe work practices and adhere to PPE requirements.Safely handle chemicals, corrosives, solvents, and other pharmaceutical compounds.Demonstrate physical ability to lift a minimum of 50 lbs. and push/pull pallets, product cans, etc. multiple times per shift. PRIMARY RESPONSIBILITIES: All responsibilities of Production Associate I AND the following:Learn to operate all relevant automation technology and equipment for labeling and visual inspection operations.Obtain and maintain visual inspection qualification for NLT 2 additional unique processes including, but not limited to:On-Q pumpsIV BagsProvide effective leadership, advice, instructions, and training to others regarding operations for labeling, visual inspection, and support processes.Demonstrate basic troubleshooting skills and the ability to make recommendations or collaborate on solutions for resolving issues.Make minor adjustment to equipment to address issues.Complete documentation reviews as required or assigned. |
| Arrive for work on-time, prepared to work in the CNC environment for the majority of each shift.Operate with Integrity by maintaining high ethical standards. Treat all employees with trust, respect, and professionalism. Speak up and hold others accountable for high integrity by providing constructive feedback. Take accountability for individual and team mistakes and participate in related corrective actions.Ensure patient safety by understanding you and your team’s impact on product quality.Excel within a diverse and high performing team. Remain open to new ideas and perspectives, communicate across shifts as required, and comply with site process to create a safe work environment. Demonstrate a passion to perform by meeting personal and departmental goals. Self-driven and self-accountable, performs required tasks, and progresses on qualifications within reasonable timelines.Demonstrate innovation abilities by identifying and speaking up about viable options for improvements and exploring and creating a path for implementation. |
| High School Diploma or equivalent.Must pass a drug test.Must speak, write, and read English.Must be a team player.Must have excellent attention to detail. |
| Prior cGMP experience.Knowledge of FDA guidelines, cGMP, and GDP.Willingness to participate in training and gain other certifications as needed.Knowledge of basic arithmetic and chemistry calculations.Ability to work in a fast-paced environment with dynamic priorities and demands.Excellent written and verbal communication skills.Desire to expand knowledge and grow with the company.Leadership ability. |
