Production Technologist - Full Time Day Shift
About the role
This vacancy has now expired. Please click here to view live vacancies.
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
Teaser label
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.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
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
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
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
Similar jobs at ICON
Salary
Location
China, Chengdu
Location
Chengdu
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR141130
Expiry date
01/01/0001
Salary
Location
US, Blue Bell (ICON)
Department
Full Service - Commercial Solutions
Location
Blue Bell
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Sales
Job Type
Permanent
Description
The Opportunity Are you a driven, strategic leader with a passion for building relationships and overcoming challenges? Do you thrive in a fast-paced environment where innovation and persistence are k
Reference
JR137305
Expiry date
01/01/0001
Author
Christopher Frank
Author
Christopher FrankSalary
Location
Brazil, Sao Paulo
Department
Clinical Monitoring
Location
Sao Paulo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking CRAs II and Senior CRAs to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials
Reference
JR140322
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana LuciaSalary
Location
Estonia, Tallinn
Location
Tallinn
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clini
Reference
JR140603
Expiry date
01/01/0001
Author
Patrick HaleAuthor
Patrick HaleSalary
Location
India, Chennai
Location
Chennai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
We are currently seeking an Accounts Receivable Manager to join our diverse and dynamic team. As the Accounts Receivable Manager, you will be responsible for overseeing all aspects of the accounts rec
Reference
JR140544
Expiry date
01/01/0001
Author
Puja JaiswalAuthor
Puja JaiswalSalary
Location
Taiwan, Taipei
Location
Taipei
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR141284
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy Tang