Process Engineer III, MSAT

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office

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. 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.

DESCRIPTION:
Join our team at Thermo Fisher Scientific as a Manufacturing Sciences Scientist III, where you'll contribute to global health through innovative process development and optimization. You'll provide technical leadership in technology transfer, process validation, and manufacturing support across our facilities. Working at the intersection of R&D and manufacturing, you'll collaborate with cross-functional teams to ensure successful execution of manufacturing processes while driving continuous improvement initiatives. Your expertise will be vital in resolving complex technical challenges, conducting investigations, and implementing solutions that maintain our high standards of quality and efficiency.

REQUIREMENTS:
• Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in GMP-regulated pharmaceutical/biotech manufacturing.
• Preferred Fields of Study: Chemical Engineering, Chemistry, Biochemistry, Biotechnology, or related scientific field
• Strong technical expertise in process development, scale-up, and technology transfer
• Proven ability to lead complex investigations and implement effective solutions
• Experience with process validation and qualification activities
• Expert knowledge of cGMP regulations and quality systems
• Advanced project management and documentation skills
• Strong analytical and statistical analysis capabilities
• Excellent verbal and written communication skills
• Ability to work collaboratively in a matrix environment
• Proficiency with statistical analysis software and Microsoft Office suite
• Experience mentoring colleagues and providing technical training
• Strong problem-solving skills and attention to detail
• Ability to support manufacturing operations as needed, including some weekend/off-hours coverage
• Travel up to 20% may be required
• Foreign language skills may be required for some locations