Production Technologist - Full Time Day Shift
About the role
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Production Technologist II
Portland, OR
The Production Technologist II is responsible for producing, testing, and packaging biological reagents and basic Laboratory solutions by following and maintaining detailed written procedures. The Production Technologist is responsible for adhering to Production protocols, QMS related procedures and activities, and support of inter-departmental objectives.
Responsibilities:
- Formulate, culture, evaluate, aliquot, label, package, and test reagents.
- Maintain supply and reagent inventory for the Production Department, including monitoring of custom reagent ordering schedule.
- Maintain knowledge and experience with full suite of Production assays, equipment, documentation, and processes, including high-complexity and newly transferred products.
- Assist in document writing and peer review in support of technology transfer activities and process improvements.
- Support Production management through generation and implementation of high level deviations, investigations, CAPAs, or validations as appropriate or assigned.
- Interactions with Enterprise systems as appropriate, including physical inventory support
- Utilize existing production protocols to generate products within specifications, including highly complex and newly transferred products and processes.
- Author, revise, or review detailed work instructions, protocols, specifications, or other product documentation as needed.
- Complete production work orders on schedule under the direction of Production management
- Create and accurately maintain production-related documents and records for production and quality assurance
Requirements
- Minimum 2 years of work experience providing relevant skill enhancements in production, manufacturing, molecular biology, or equivalent.
- Technology transfer/assay development experience preferred.
- Bachelor's degree in Molecular Biology, or related biology field(s), or equivalent combination of education and experience as needed to execute all job duties.
Benefits of Working in ICON
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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12/01/2025
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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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11/28/2025
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Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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