Danaher Corporation Project Coordinator I (Remote) in New York, New York
Aldevron is an industry pioneer with a core competency in manufacturing for gene and cell therapy. We supply high-quality plasmid DNA, mRNA and proteins to our clients, who are breaking new ground on the world’s most important and challenging solutions to benefit us all. We're looking for innovative, forward-thinking individuals who share our goals of advancing science and making an impact on the world.
Aldevron is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
The Project Coordinator I serves as an integral part of the Project/Program Management Department, supporting campaign lifecycles with Project Managers as well as Client Relations personnel. This support role is responsible for mining requisite information for production quotes included in the Statement of Work (SOW), drafting and routing specification forms, coordinating meetings, assembling agendas, and capturing decisions and actions of internal and client-facing meetings. This position interfaces with multiple departments in order to contribute to the preparation and delivery of high-quality information to clients and internal colleagues for the accurate launch and success of projects. This position supports Project Management and Client Relations team members
Support official initiation of projects through interface with Aldevron’s ERP system, creating accurate sales orders and Lot Number details
Obtain familiarity with SOW’s for use in Manufacturing Specification Form
Assembly and timely updates of internal project timelines
Assist Client Relations colleagues with generation of storage and stability quotations and specification forms.
Coordinate meetings, assemble agendas, capture decisions and actions through minutes held either internally or with the client
Interface with Aldevron IT to ensure appropriate and client specific document repositories, such as SharePoint, are functioning and available for collaborative use with clients
Maintain documentation in accordance with GDP and internal SOPs
Assist with drafting and routing of business and specification documents, as necessary
1 year of experience in a biotechnology, pharmaceutical, or medical device related field preferred
Experience within a regulated environment (GMP, FDA, ICH) preferred
B.S. preferred; scientific degree preferred
When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at email@example.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.