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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.

This position is part of the Research and Development Department located in Fargo, ND and will be on-site. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development (AMD) and report to the Principal Scientist responsible for development and optimization of analytical methods that will be used for investigative testing, GMP release testing, and stability testing of Aldevron Products (e.g., nucleic acids, lipid nanoparticles).

In this role, you will have the opportunity to:

• Independent ly, propose, lead, and oversee the development of analytical methods such dPCR, CGE, spectrophotometry, ELISA, and HPLC in the laboratory and through collaboration with internal and external stakeholders. Ensuring that methods are robust and fit-for-purpose as release tests for GMP Quality Control.

• Provide input to or create project timelines, provide updates to management, and adhere to those timelines.

• Provide technical support for activities associated with method validations and transfers including development of validation strategies to meet regulatory requirements. This includes creating, revising, and finalizing standard operating procedures (SOP), study protocols, study reports, product specifications, and other GMP documents.

• Serve as a subject method expert to junior scientific staff regarding enhanced approaches to analytical procedure development and lifecycle management. This includes but is not limited to generating control strategies for new analytics, proposing purposeful experiments to guide method development, and provide recommendations to optimize procedures for subsequent validation.

• Identify and implement new techniques and instrumentation to expand internal capabilities. Prepare justifications for capital expenditures (e.g., new laboratory instruments). Prepare purchase orders and coordinate authorization, procurement, and implementation.

The essential requirements of the job include:

• Ph.D. in biology, molecular biology, chemistry, biochemistry, or related scientific field with minimum 3 years of relevant industry experience or master’s degree with minimum 5 years of relevant industry experience or bachelor’s degree with minimum 8 years of relevant industry experience required. Relevant experience consists of working in assay development and/or validation, optimization, experimental design, and data analysis in a regulated industry (cGMP).

• Ability to independently propose and lead analytical method development projects with purposeful experimental design and the ability to anticipate results that drive towards the conclusions necessary for successful assay development: a successful track record of analytical method development that leads to method validation.

• Good communication skills are essential as this position is expected to develop high level presentations to large and diverse internal and external audiences serving as a key liaison and champion of method development projects.

• Excellent troubleshooting ability to support both analytical development work and Quality Control OOS/OOT investigations as subject matter expert.

• Must be able to develop solutions for simple and complex problems, which require a high degree of ingenuity, creativity, and innovation.

It would be a plus if you also possess previous experience in:

• Strong understanding of regulatory guidelines, such as ICH, FDA, EMA, or compendia.

• Previous experience working directly with DNA, RNA, and/or lipid nano particles.

• Proven track record of leading scientific teams is a plus.

#LI-LM1.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

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.