Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

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:
At Thermo Fisher Scientific, join our collaborative team as a Sr Technical Operations Engineer, where you'll contribute to developing and manufacturing biopharmaceutical products. You'll apply your technical expertise to ensure the highest quality standards while working with advanced technologies and processes. This position offers the opportunity to work with cross-functional teams, enhance processes, and contribute to therapies that help improve global health and environmental sustainability.

You will manage technical projects, provide manufacturing support, and resolve complex process challenges while ensuring compliance with GMP regulations. Your role will involve developing and optimizing formulation processes, conducting validation studies, and working closely with clients and internal teams to deliver excellent results. This position offers professional development opportunities within our organization that values integrity, dedication, collaboration, and innovation.

REQUIREMENTS:
• Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in biopharmaceutical manufacturing or related industry
• Preferred Fields of Study: Chemistry, Biochemistry, Biology, Biotechnology, Chemical Engineering, or related scientific field
• Additional certifications in Production and Inventory Management (CPIM) or related areas are beneficial
• Strong understanding of GMP regulations and quality systems
• Expertise in process validation, risk assessments, and process control strategies
• Proficiency in manufacturing documentation systems and batch record review
• Experience with technology transfer and scale-up processes
• Strong analytical and problem-solving abilities
• Excellent project management and organizational skills
• Outstanding written and verbal communication capabilities
• Ability to work effectively in a matrix environment with cross-functional teams
• Proficiency in English required; additional language skills beneficial
• Availability for flexible scheduling including on-call duties when required
• Demonstrated leadership abilities and mentoring skills
• Knowledge of Lean Manufacturing and Six Sigma methodologies
• Strong attention to detail and commitment to quality standards