Job Description:

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
Quality
Control

and may
be located in

Fargo, ND or Madison, WI
.
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

Quality
Control
Stability team

and report to the

Senior Director of Quality Control
.

In this role, you will have the opportunity to:

• 
  

  
  
  Lead, mentor, and develop a team of
  S
  tability
  Specialist
  

  
  

• 
  

  
  
  Ensure
  timely
  and
  accurate
  
  Stability
  documentation
  , including protocols,
  timelines
  and summary reports.
  

  
  

• 
  

  
  
  Develop, implement, and manage stability programs
  in accordance with
  regulatory requirements (e.g., ICH guidelines) and company policies.
  

  
  

• 
  

  
  
  Implement and
  maintain
  Stability department standard operating procedures
  .
  

  
  

• 
  

  
  
  Manage stability projects from
  inception
  to completion, ensuring timelines and milestones are
  meet
  .
  

  
  

• 
  

  
  
  Collaborate with cross-
  functional
  teams, including Quality Assurance, Tech Ops, and Regulatory Affairs.
  

  
  

The essential requirements of the job include:

• 
  

  Bachelor's degree in Scientific/ Technical related field
  required
  

  
  

• 
  

  Minimum of 3-5 years of GMP experience, preferably in a Life Sciences/CDMO industry.

  
  


• 
  

  1 year of supervisory/leadership experience.

  
  

It would be a plus if you also
possess

previous
experience in:

• 
  

  Knowledge of root cause analysis tools and risk management tools (5 whys, 6M etc..)
  in a
  compliance
  industry
  

  
  

• 
  

  Proficiency
  in laboratory information systems (LIMS)
  

  
  

• 
  

  Experience with interactions with regulatory agencies.
  

  
  

#LI-GC1

Join our winning team today. Together, we'll 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.

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.

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.

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