EXPLORE YOUR NEXT CHAPTER
mRNA Project Manager
Thermo Fisher Scientific
Source: Headcount Labs · original listing ↗
Job data: Headcount Labs, ODbL 1.0. Job descriptions belong to their employers.
Posted 2 days ago
About this role
Work Schedule Standard (Mon-Fri) Environmental Conditions 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 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: Completion 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