Project Manager
at Thermo Fisher Scientific
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Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsOfficeJob DescriptionAs 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.Responsibilities:Manage, execute and coordinate technical and process-related (sub-)projects within the Project Engineering Organization.Responsible for scope, budget, safety, quality and schedule of assigned tasks.Collaborate with teams across the organization to drive effective project execution.Perform engineering tasks and support construction and commissioning/qualification on Process topics within the Project Engineering Organization.Assure timely delivery of engineering related activities and documents throughout entire project life cycleNavigate ambiguity and guide teams effectively within a matrix environment.Support business growth and operational excellence through successful project outcomes.Requirements:Bachelor’s or Master’s degree in Chemical Engineering, Bioprocess Engineering, Mechanical Engineering, Biotechnology, or related technical fieldProvide technical expertise in biologics manufacturing processes (e.g., cell culture, fermentation, purification, single-use systems, clean utilities)Support equipment specification, vendor selection, FAT/SAT execution, and commissioning activitiesLeadership abilities with proven success guiding teams through influenceEffective communication and interpersonal skills, with ability to work with all levelsExperience managing project budgets, timelines, risks and stakeholder expectationsStrong organizational and analytical skills with attention to detailAbility to manage multiple high-priority projects simultaneouslyBusiness acumen and strategic mindsetProblem-solving abilities and proactive approach to risk mitigationProficiency with MS Office suite and project management softwareExperience in regulated industry (e.g. pharmaceutical, medical device) preferredKnowledge of GMP/GLP, ISO and other relevant quality standards preferredEnglish communication proficiency required, additional languages a plus
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