QC Chemist

Quality Control Chemist II

The Opportunity 

This role supports analytical testing and quality assurance functions in a regulated nutraceutical environment, with additional responsibility for cross-functional specification alignment and technical problem-solving. The QC Chemist II operates independently, leads investigations, and collaborates directly with R&D to optimize product quality and compliance. This role is intended for high performing professionals with technical depth and initiative beyond standard Chemist I expectations.

What You’ll Do

• Independently perform validated analytical methods (e.g., HPLC, LC/MS, UV-VIS) for raw
  materials, in-process blends, and finished products.
• Lead out-of-specification (OOS) investigations, including root cause analysis and
  documentation of findings.
• Liaise with R&D on formulation challenges and specification improvement opportunities.
• Perform method evaluation and data analysis to support continuous improvement initiatives.
• Research technical literature or internal studies to inform test methods or troubleshoot
  anomalies.
• Draft and revise SOPs, protocols, and test procedures in collaboration with QC Chemist III.
• Support internal audits and CAPA resolution with technical documentation.
• Train junior chemists on method execution and good documentation practices.

The Skills You Will Bring To The Team

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, or related field.
• 2+ years hands-on laboratory experience in a GMP-regulated quality control setting.
• Demonstrated ability to independently operate analytical platforms (e.g., HPLC, LCMS, UVVIS).
• Prior experience leading investigations or authoring deviation documentation preferred.
• Strong understanding of analytical chemistry and regulatory quality requirements (GMP, FDA,ICH)
• Able to interpret data and identify specification gaps or improvement areas.
• Self-directed, highly organized, and detail-oriented.
• Strong communication skills, including ability to interface with R&D and QA teams.
• Proficiency in MS Office and familiarity with LIMS or digital lab systems is preferred.
• Highly organized, detail-oriented, and independently driven.
• Independent, proactive, extremely detail oriented, dependable, organized and ability to handle multiple tasks.
• Must be able to work flexible hours to include overtime and weekends when needed.
• Strong desire and ability to work in fast paced deadline orientated environment.
• Fluent in written and spoken English required
• Must be able to communicate to and work well with multiple departments.
• Must be results focused and oriented toward accomplishment of team goals.

Where And How You Will Work

The opportunity will be based onsite in West Haven, Connecticut.

What we would like to offer you!  

The opportunity to develop your career on a global stage, continuous learning through an on-demand learning platform, and a competitive compensation package including staff discounts, generous family leave policy, health & dental plan, competitive salary, 401K. Factors that could be used to determine your actual salary may include your specific skills, years of experience and comparison to current employees already in this role. 

Apply now and make a difference in the world of health and wellness!

Glanbia has a unique portfolio of better nutrition brands and ingredients, addressing growing consumer demand in major health and nutrition categories. We play into the growing market trends of active lifestyles and, health and wellness.

At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. 

At Glanbia, our culture celebrates individuality, knowing that together we are more.