高级工程师,流程验证
Senior Engineer, Process Validation
让创新更有价值。
你是否准备好加速自己的潜力,在生命科学、诊断和生物技术领域做出真正的改变?
在Aldevron,Danaher的15多家运营公司之一,我们的工作拯救生命——我们所有人都致力于通过创新实现切实的影响。
你会在一个充满归属感的文化中茁壮成长,你的独特观点至关重要。通过利用Danaher的持续改进体系,你将帮助把想法转化为影响——以生命的速度进行创新。
在Aldevron,我们提供世界级的CDMO服务,加速突破性疗法的开发。我们的使命是成为基因组医学先驱的创新引擎。作为我们团队的一员,你将帮助实现改变生命的创新——影响全球数百万人。我们汇聚深厚的科学专业知识、对质量的坚定承诺以及协作精神,推动进步。无论你是刚刚开始职业生涯,还是拥有多年经验,我们都重视你带来的独特视角。加入我们,成为一支以使命为导向的团队,推动科学进步,释放人类潜能——一次发现一个突破。
了解Danaher业务体系,它使一切成为可能。
高级工程师,工艺验证负责领导和支持内部和外部的验证项目,这些项目有助于关键新救命药物的商业化。
该职位向工艺验证经理汇报,属于位于北达科他州法戈的技术运营部门,并且是完全远程办公。
在这个职位上,你将有机会:
- 在工艺验证的三个阶段设计、执行并总结交付成果,支持工艺特性分析和确认,涵盖关键起始物料、原料药和制剂,产品分类符合FDA指南、欧盟GMP附录15和生命周期方法。
- 领导无菌灌装-封口工艺验证策略和确认项目的计划、执行及生命周期管理,包括无菌过滤、无菌工艺模拟、无菌灌装、目检、容器密封完整性测试、滤器验证、标签、包装和运输。
- 采用基于风险的方法,使用工具如pFMEA、风险排序和关键性评估,并应用统计工具评估工艺性能,包括但不限于过程能力分析等。
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Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time.
Learn about the Danaher Business System which makes everything possible.
The Senior Engineer, Process Validation is responsible for leading & supporting internal and external validation projects that enable commercialization of vital new life saving medicines.
This position reports to the Process Validation Manager and is part of the Technical Operations Department located in Fargo, ND and will be fully remote.
In this role, you will have the opportunity to:
- Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
- Lead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping.
- Drive risk-based approaches using tools such as pFMEA, risk ranking, and criticality assessments and apply statistical tools to evaluate process performance, including but not limited to process capability, trend analysis and control charts and DOE) interpretation.
- Serve as a technical SME for process validation with external clients, across internal teams such as MSAT, manufacturing, QC, QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.
- Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design
The essential requirements of the job include:
- Bachelor or master degree in engineering and 5+ years of experience
- Prior experience in leading process development, engineering, and deliverables across all three stages of process validation in biologics/small and large molecules manufacturing train using statistical analysis, risk assessment, and process improvement tools required.
- Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and practices.
- Proficiency in technical writing with deviation investigations, root cause analysis, and risk assessments.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
· Ability to travel 15% to site to support validation project executions, routine inspections, audits, and client visits.
It would be a plus if you also possess previous experience in:
- Packaging and shipping validation of final product container closure configurations.
- Client facing roles such as prior experience in a CDMO environment
Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
At Aldevron we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Aldevron can provide.
The annual salary range for this role is $100,000 to $130,000. 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 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 Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
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 .
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Originally posted on Himalayas