Stability Specialist

Molecular Devices

Molecular Devices

Fargo, ND, USA
Posted on Thursday, July 11, 2024

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 Department located in Fargo, ND and will be working onsite. 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 Team and report to the Senior Manager, Stability, responsible for Writing and maintaining stability protocols and SOPs in support of the stability program.

In this role, you will have the opportunity to:

  • Responsible on the implementation of regulatory requirements for the stability program documentation. Responsible of routing for approval of the stability program documents.

  • Organize, assemble, and route documentation to support Stability Program document review and approval as required by Quality Systems management.

  • Ensure data is evaluated, including the creation, review, and trending, to meet company, industry and regulatory requirements.

The essential requirements of the job include:

  • High School Diploma or equivalent GED required. Bachelor's Degree with a focus in Chemistry, Life Sciences, Pharmacy or similar discipline preferred.

  • 2 years of experience in a relevant professional field.

  • Experience in a Quality Assurance or Quality Control function in a regulated industry (Pharmaceutical, Medical Device, OTC Drug, Cosmetic, cGMP etc.) preferred

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.

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.