Contract
Bioprocess Manufacturing Technician – Vaccine Production
Location: Athens, GA
Duration: 6 months contract
Industry: Pharmaceutical / Biotechnology / Vaccine Manufacturing
Shift Schedule: M-F, 8 am - 5pm
Position Summary :
We are seeking a Bioprocess Manufacturing Technician – Vaccine Production to support vaccine manufacturing operations within the Tank and Central Services department. This role is responsible for performing critical process support activities to ensure the safe and sterile preparation of equipment used in vaccine production.
The ideal candidate will have experience in a regulated manufacturing environment, strong attention to detail, and the ability to follow Standard Operating Procedures (SOPs) while maintaining compliance with cGMP and USDA requirements.
Key Responsibilities
• Perform process support activities associated with vaccine manufacturing operations.
• Support production schedules by following Tank and Central Services scheduling requirements.
• Execute Steam-In-Place (SIP) processes and Clean-In-Place (CIP) procedures for mobile process equipment.
• Prepare, sterilize, and decontaminate process equipment, garments, and roller bottles through autoclaving processes.
• Ensure all manufacturing activities are performed in compliance with established SOPs, cGMP guidelines, and safety requirements.
• Review in-process documentation for accuracy, completeness, and compliance.
• Maintain technical records, production documentation, and supporting process data.
• Assist with training and coaching of new and existing employees on required manufacturing processes.
• Participate in troubleshooting activities, root cause investigations, and implementation of corrective and preventative actions (CAPA).
• Escalate production issues and process interruptions appropriately.
• Support site projects, continuous improvement initiatives, deviations, and change control activities.
• Demonstrate commitment to Environment, Health, and Safety (EHS) programs and initiatives.
• Participate in continuous improvement activities and performance improvement initiatives.
Required Qualifications
• High School Diploma or equivalent required.
• Previous experience in pharmaceutical, biotechnology, laboratory, or regulated manufacturing environments preferred.
• Working knowledge of cGMP requirements and USDA regulations related to vaccine or biologics manufacturing.
• Ability to follow detailed procedures and maintain accurate documentation.
• Strong attention to detail and commitment to quality and compliance.
• Basic math skills and ability to perform process calculations.
• Ability to troubleshoot equipment and process-related issues.
• Proficient computer skills, including Microsoft Office and database systems.
• Strong verbal and written communication skills.
• Ability to work effectively in a team-oriented manufacturing environment.
• Ability to manage priorities and meet deadlines in a fast-paced production environment.
Preferred Experience
• Vaccine manufacturing experience.
• Biopharmaceutical manufacturing experience.
• Cleanroom operations.
• Aseptic processing.
• CIP/SIP operations.
• Autoclave sterilization.
• Pharmaceutical production support.
• Experience working in FDA, USDA, or GMP-regulated environments.
Skills & Competencies
• GMP Documentation
• Sterile Processing
• Equipment Preparation
• Autoclave Operations
• Clean-In-Place (CIP)
• Steam-In-Place (SIP)
• Manufacturing Documentation
• Process Troubleshooting
• Deviation Management
• CAPA Support
• Safety Compliance
• Continuous Improvement
• Team Collaboration
Education
Required: High School Diploma or equivalent
Preferred: Technical training, laboratory experience, or manufacturing experience