Job Information
Danaher Corporation Technical Project Manager II in Fargo, North Dakota
At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences.
Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
Job Summary:
The Technical Project Manager II is responsible for managing complex projects in focus areas in support of client programs and services. This role requires knowledge of GMP biomanufacturing operations to effectively collaborate with cross-functional stakeholders and deliver projects on time and on budget.
Responsibilities:
Manage complex technical projects
Serve as liaison between stakeholders
Work collaboratively with the Project/Program Manager(s) and clients to communicate regular project updates
Relay cost impacting project changes to the Client Services team
Work collaboratively with internal stakeholders to ensure on-time and on-budget completion of key milestones, action items, and project deliverables
Proactively identify barriers to success and work with cross-functional team members to generate and implement solutions
Collect and report metrics related to timeline and budget
Effectively navigate and resolve conflict with internal and external stakeholders to maintain and nurture relationships
Closely track and forecast tasks and project timelines as well as provide team with early warnings on possible variances
Qualifications:
Bachelors d egree in related area of study required
5 years of experience in method development/validation, QC, biomanufacturing related validation, process development, or tech transfer initiatives required, preferably related to nucleic acids
Experience leading an industry relevant department and /or complex projects
Thorough understanding of cGMP requirements and compliance
PMP Certificate 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 applyassistance@danaher.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.