QC Analyst II
Longmont, CO
Quality Control – Quality Control (Ingr.) /
Full-Time /
On-site
About Niagen Bioscience
Niagen Bioscience (NASDAQ:NAGE), the parent company of ChromaDex, is a global bioscience company dedicated to advancing NAD+ research and healthy-aging science. Our scientists partner with leading universities and research institutions worldwide to discover, develop, and create solutions that help people age better. Our flagship ingredient, Niagen®, a patented form of nicotinamide riboside, is one of the world's most extensively researched and validated NAD+ precursors, backed by 35+ human clinical trials and 400+ peer-reviewed studies.
We offer two product brands: Tru Niagen®, a daily supplement clinically proven to increase NAD+ levels; and Niagen® Plus, our premium pharmaceutical-grade NAD+ therapy brand featuring Niagen™ IV and injectables.
As pioneers in NAD+ technology, Niagen Bioscience and ChromaDex continue to set the Gold Standard in scientific rigor, quality, safety, and transparency through our commitment to excellence, innovation, and integrity. We have two locations in California (Tustin, CA and Westwood, CA) and a premier research laboratory in Longmont, CO.
Our C.H.E. (pronounced chi)
We enjoy working with like-minded people who embody “C.H.E.” and share our passion for health, wellness, discovery, and innovation. In our collaborative environment, employees quickly adapt to different situations, bringing:
Character – A positive attitude, commitment to success, and strong ethics.
Horsepower – Good judgment, creative problem-solving, and a strong work ethic.
Experience – Functional knowledge and skills to perform efficiently.
If you're eager to work with incredible people and contribute to something meaningful, join our team and help shape the future of bioscience on a global scale!
What we Offer:
A competitive salary, affordable health benefits, company sponsored life insurance, wellness initiatives, retirement savings with company match, paid time off, career growth opportunities and a flexible/hybrid work environment.
Core Expectations:
· Conduct qualitative and quantitative chemical analyses using instruments such as HPLC, UHPLC, TOF-MS, GC-MS/FID using liquid and headspace injections, NMR, and Karl Fischer titration
· Execute other testing techniques including Loss on Drying, Bulk and Tapped Density, Particle Size Distribution, Flowability assessments, and organoleptic testing of consumer products and ingredients
· Assist in the development, validation, and verification of analytical methods in collaboration with the R&D team
· Prepare and analyze calibration curves, internal and external standards, and QC checks
· Create and validate calculation and reporting tools (e.g., spreadsheets) to streamline data processing and improve consistency
· Perform instrument maintenance (PM/OQ) and identify and troubleshoot technical issues with equipment and methods especially on HPLC and GC instruments
· Author and review Certificates of Analysis and other technical documents such as SOPs, deviations, and out-of-spec investigations
· Support training and onboarding of junior analysts and contribute to team knowledge sharing with peers, including reviewing data and reports and providing feedback to other analysts
· Monitor laboratory supply levels and request consumables to maintain uninterrupted testing operations
· Comply with all SOPs, safety protocols, and regulatory standards including GMP and ISO 17025 requirements
Qualifications and Success Factors:
· Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline
· 3+ years of hands-on experience in an analytical laboratory setting, including method development and validation
· Experience handling both solid and liquid sample matrices and operating a variety of laboratory instruments, especially HPLC and GC
· Strong familiarity with software tools such as Agilent ChemStation, ChemDraw or similar software
· Demonstrated proficiency in GMP-compliant lab practices, technical documentation, and report writing
· Comfortable in a laboratory environment handling hazardous chemicals; adherence to safety protocols and use of PPE
· Must maintain accurate and compliant lab notebook, records, and follow GDPs
Competencies & Skills
· Effective trainer and mentor with a collaborative work style
· Solid troubleshooting and analytical thinking capabilities
· Quick learner with the ability to adapt to technical challenges
· Independent worker with time management and prioritization skills
· Technically proficient in MS Office (Excel, Word), eQMS/LIMS, and other scientific software
· Strong verbal and written communication skills across all organizational levels
· Must be capable of lifting up to 30 lbs and performing repetitive tasks efficiently
*** The Salary range for this position is $65,000 - $85,000 and is located at our lab in Longmont, CO ***
$65,000 - $85,000 a year
We are an equal opportunity employer that operates with an emphasis that People Matter. We respect and will consider every and all kinds of people regardless of race, color, religion, sex, sexual orientation, gender identity, age, natural origin, protected veteran status, disability, or any other factors prohibited by law or humanity.
