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      Role Summary
 The Vaccine Manufacturing Facility Production Associate supports vaccine manufacturing operations, performing aseptic processing and related activities within a day-shift, 12.5-hour rotation environment. This role emphasizes safety, quality, and adherence to GMP in a self-directed team setting.
 
 Responsibilities
 
 - Perform manual and automated processing of vaccine manufacturing equipment and support functions necessary for production.
 
 - Execute documentation and clerical tasks to ensure accountability and traceability of product.
 
 - Maintain, inventory, and transport required processing equipment, materials, supplies, and products.
 
 - Operate computer-controlled process equipment (e.g., washer, autoclave, vial filler, lyophilizer, capping/inspect machines).
 
 - Assist in equipment troubleshooting.
 
 - Maintain cleanliness; perform facility sanitization and decontamination per procedures.
 
 - Complete in-process testing and inspections to support manufacturing, validation, and development.
 
 - Identify and address compliance, environmental, safety, and process deviations; escalate as needed.
 
 - Prepare and maintain equipment used in the vaccine manufacturing process.
 
 - Schedule and perform environmental monitoring; record results in the database; deliver samples to laboratories and coordinate with Quality and Logistics.
 
 - Participate in safety, housekeeping, 5S, kaizen events, and other trainings/initiatives; serve on safety and quality committees as required.
 
 
 
 Qualifications
 
 - Education: High School Diploma or equivalent required; Bachelor's degree in Life Science or Engineering or Associate’s in Life Science or Engineering with at least 2 years relevant experience preferred.
 
 - Experience/Skills: Willingness to work 12-hour day shifts on a 2-2-3 schedule; successful completion of aseptic gowning qualification; ability to lift 50 lbs; willingness to work various shifts; basic computer literacy (internet, email, word processing).
 
 - Preferred: Bachelor’s or Associate’s degree in Life Science or Engineering; BioWorks Certificate; experience with SAP/Manufacturing systems; experience with Electronic Batch Records; experience with Environmental Monitoring and Sampling.
 
 
 
 Skills
 
 - Accountability, Analytical Problem Solving, Computer Literacy, Environmental Monitoring, GMP Operations, Life Science, Manufacturing Processes, Production Scheduling, SOP Writing, Vaccine Production