Environmental Conditions Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed
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.
- Must be legally authorized to work in the United States WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
- Must be able to pass a comprehensive background check, which includes a drug screen.
12-hour night shift (2/2/3 schedule) 6PM – 6AM with 15% shift differential
This role is part of a team providing 24/7 technical support and expertise to sterile pharmaceutical production. You will support customer-facing process engineers, assist with technical transfers, and drive continuous improvement initiatives to enhance safety, quality, and operational efficiency.
This position plays a critical role in minimizing equipment downtime, improving Overall Equipment Effectiveness (OEE), and ensuring compliance with regulatory and cGMP standards.
- Provide technical support to meet business objectives and improve production OEE
- Diagnose and resolve complex process and equipment issues
- Serve as Subject Matter Expert (SME) on equipment and process functionality
- Develop process flow diagrams, troubleshooting guides, and training materials
- Support CAPEX equipment upgrades for sterile fill/finish operations
- Coordinate planned shutdowns and production interruptions
- Create, modify, and approve process equipment recipes in compliance with SOPs
- Support investigations by providing data and recommending improvements
- Collaborate daily with Engineering, Operations, Maintenance, Quality, and Safety teams
- Spend 70–90% of time on the production floor supporting operations
- Document work activities and maintain accurate records
- Drive continuous improvement using TPM, 5S, PPI, and data-driven metrics
- Associate’s degree in mechanical, electrical, or industrial engineering with a minimum of 3 years of process experience. A combination of experience and education will be considered.
- Experience in regulated manufacturing (pharmaceutical, biotech, or medical device) preferred
- Process improvement experience (Lean, Six Sigma, 5S, trend analysis) preferred
- Strong troubleshooting and analytical skills
- Knowledge of data integrity principles and automation systems preferred
- Excellent communication and collaboration skills
- Strong organizational skills and attention to detail
- Ability to manage priorities in a fast-paced production environment
- Adherence to all Environmental Health & Safety (EHS/OHS) policies
- Commitment to maintaining a safe and compliant workplace
- Flexibility to support shift-based production operations
- Other duties as assigned
Join us and be part of a team that is driving innovation in sterile pharmaceutical manufacturing while making a real-world impact.