Mrna Project Manager

01 ago - Bardi
Thermo Fisher Scientific

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
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 an mRNA Project Manager, where you'll manage projects that advance scientific discovery and improve health outcomes. You'll oversee multiple sophisticated projects simultaneously, coordinating cross-functional teams to ensure successful execution of technology transfers, product development, and process improvements. Working closely with clients and internal stakeholders, you'll guide projects from conception through completion while maintaining the highest standards of quality and regulatory compliance. This role offers exposure to advanced technologies and the opportunity to contribute to meaningful innovations.
REQUIREMENTS:




Typically requires 5 years of previous related experience and a general knowledge of the Parmaceutical/ Biotechnologies proven experience. Equivalent combinations of education, training and meaninful work experience may be considered.
Preferred Fields of Study: Comepletion of a MSc or its equivalent (depending of the country) in a scientific/pharmaceutical area (Chemistry, Pharmacy, Biotechnology, Engineering, or related scientific field)
PMP certification is a plus
Strong knowledge of GMP regulations and pharmaceutical manufacturing processes
Excellent project planning, execution, and tracking capabilities
Proven ability to manage multiple complex projects simultaneously
Strong client relationship management and communication skills
Proficiency in Microsoft Office suite; experience with project management software
Fluent English required; additional language skills valued
Experience with cross-functional team leadership and matrix management
Strong analytical and problem-solving abilities
Knowledge of pharmaceutical development, clinical trials, and technology transfer processes
Ability to work effectively in a regulated environment
Detail-oriented with excellent organizational and documentation skills
Strong risk management and decision-making capabilities
Experience with budget management and resource planning
Ability to influence and negotiate with stakeholders at all levels

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