Production Engineer - Nights (2-2-3) Schedule

Thermo Fisher Scientific•Greenville, NC

4d•Onsite

About The Position

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. Excellent Benefits Package Review our company’s Total Rewards Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Holidays 401K Company Match up to 5% Tuition Reimbursement – eligible after 90 days! Employee Referral Bonus Employee Discount Program Recognition Program Charitable Gift Matching Company Paid Parental Leave Career Advancement Opportunities Location/Division Specific Information Greenville, NC RELOCATION ASSISTANCE IS NOT PROVIDED 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 Discover Impactful Work: 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. A Day in the Life: 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 Join us and be part of a team that is driving innovation in sterile pharmaceutical manufacturing while making a real-world impact. Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Requirements

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.
Strong troubleshooting and analytical skills
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
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.

Nice To Haves

Experience in regulated manufacturing (pharmaceutical, biotech, or medical device) preferred
Process improvement experience (Lean, Six Sigma, 5S, trend analysis) preferred
Knowledge of data integrity principles and automation systems preferred

Responsibilities

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