Process Validation Engineer II
Process Validation Engineer II
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Job Description
At Aldevron we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated forwardthinking associates share this goal by combining bestinclass 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.
The Process Validation Engineer II is part of the Technical Operations Department located in Fargo ND and will be onsite. At Aldevron we combine bestinclass products and servicewith the ideal operating environment to lay the groundworkfor vital new discoveries worldwide. You will be a part of the Process Validation team and report to the Process Validation Manager responsible for leading & supporting internal and external validation projects.
In this role you will have the opportunity to:
- Develop and review validation documents for facilities equipment and processes.
- Ensure all documents comply with corporate standards and regulatory requirements.
- Collaborate on experiments for new or modified manufacturing processes and equipment.
- Analyze critical data and provide informed recommendations.
- Support all phases of the validation life cycle including research development and continuous monitoring.
The essential requirements of the job include:
- Bachelors degree in Engineering or Scientific field (preferably Chemical Biology or Microbiology) and 4 years of experience in process development and/or technology transfer OR Associate degree in Engineering Technology or related field with 6 years of process development experience in a life sciences company
- Knowledge of regulatory and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
It would be a plus if you also possess previous experience in:
- Authoring executing and summarizing process validation lifecycle documents for stages 1 2 and 3.
- Technical writing involving quality investigations root cause analysis and risk assessment.
The salary range for this role is $75000 to $95000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer a comprehensive package of benefits including paid time off medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.
Join our winning team today. Together well accelerate the reallife impact of tomorrows 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.
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 to request accommodation.
Employment Type
Full-Time
