Production Engineer (2-2-3 schedule Days)

JOB DESCRIPTION

Work Schedule

12 hr shift/nights

Environmental Conditions

Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed

Job Description

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 day shift (2/2/3 schedule) 6AM – 6PM

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

Keys to Success:

Education/Experience

• 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

Knowledge, Skills, Abilities

• 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

Additional Requirements:

• 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.