Manufacturing Technician II - Component Prep 1st Shift

About the role

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. The Component Preparation Technician supports manufacturing operations by ensuring equipment, filters, components, and manufacturing materials are properly prepared and available for use. This position works in a regulated manufacturing environment and plays an important role in maintaining operational readiness and compliance with current Good Manufacturing Practices (cGMP).

Responsibilities

As a Component Preparation Technician, you will help ensure manufacturing teams have properly cleaned, tested, prepared, and documented equipment and materials needed to execute production activities. Your attention to quality, safety, and compliance will directly support reliable manufacturing operations and the delivery of products that meet our customers’ needs.

• Perform integrity testing and other required testing of filters in accordance with approved procedures, specifications, and manufacturing requirements.
• Wash, clean, sanitize, and prepare manufacturing equipment, components, utensils, and related items for use in production.
• Prepare, stage, assemble, and distribute manufacturing materials and components according to production schedules and approved procedures.
• Operate component preparation and cleaning equipment in accordance with standard operating procedures (SOPs), work instructions, and safety requirements.
• Inspect equipment, components, and materials before and after preparation to verify cleanliness, condition, identification, and readiness for use.
• Complete batch records, equipment logs, cleaning records, filter testing documentation, and other required GMP documentation accurately and in real time.
• Maintain appropriate status identification and segregation of clean, dirty, prepared, and unprepared equipment and materials.
• Follow established cGMP, Good Documentation Practices (GDP), Environmental Health and Safety (EHS), and site procedures.
• Identify and