Start Date
Immediate
Expiry Date
23 Nov, 25
Salary
82000.0
Posted On
23 Aug, 25
Experience
3 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Environmental Monitoring, Microbiology, Ema, Communication Skills, Biotechnology, Technical Writing, Regulatory Requirements, Data Analysis, Aseptic Technique, Iso
Industry
Pharmaceuticals
ABOUT INVENTPRISE
At Inventprise, developing innovative and widely available vaccines is in our DNA. By producing targeted vaccines for populations worldwide, we’re addressing global health inequalities and empowering people to live healthy lives—no matter where they live. Headquartered in Redmond, WA, our goal is to deliver affordable, effective vaccines at large-scale to Low and Middle Income Countries, as well as populations in the U.S. and around the world. Inventprise is committed to creating a diverse and inclusive workplace, where our people are inspired to do their best work. We’re proud to have some of the world’s most qualified industry scientists, researchers, and manufacturing professionals on our team, and strive to create a vibrant, dynamic presence in the Washington State Life Sciences environment.
REQUIRED EDUCATION AND QUALIFICATIONS:
OUR PEOPLE-FIRST PHILOSOPHY
At Inventprise, you’ll be part of a world-class team working on innovative vaccines and technologies that have global impact. Our people are an integral part of our strategy, allowing us to grow as a company and improve our performance year-over-year.
Our company was built on the belief that by working together, we have the ability to make the world a better place and improve lives. We have a growth mindset and are constantly looking for ways to enhance our contributions to improve global health. We believe that when we support each other and set high standards, we are able to do our best work.
How To Apply:
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The Quality Control (QC) Analyst II - Microbiology will support the QC Micro team by performing, coordinating, and analyzing environmental monitoring activities and data in a cGMP-regulated biopharmaceutical environment. This role is responsible for performing routine and non-routine microbiological testing, supporting all cGMP activities and practices and contributing to continuous improvement initiatives. The Analyst II will work independently with minimal supervision and provide technical input to support manufacturing and quality operations.