What are the responsibilities and job description for the Quality Control Analyst II position at Hartmann Young?
Quality Control Analyst II
📍 Albany, New York (On-site) - Relocation available for US citizens
Hartmann Young is partnered with a leading global CDMO supporting pharmaceutical and biotechnology companies in the development and manufacture of small molecule therapies.
We're looking for a Quality Control Analyst II to join an established analytical laboratory, supporting the testing of raw materials, in-process samples, finished APIs and stability studies while contributing to method development and continuous improvement initiatives.
The Role
As a Quality Control Analyst II, you will:
- Perform analytical testing of raw materials, intermediates, finished products and stability samples
- Operate a range of analytical instrumentation including HPLC, UPLC, GC, UV/Vis, IR and wet chemistry techniques
- Support method development, method transfers, qualifications and validations
- Investigate laboratory deviations and out-of-specification (OOS) results
- Assist with cleaning validation studies and analytical data review
- Contribute to laboratory equipment maintenance, calibration and audit readiness
- Provide technical support to other laboratory team members and contribute to continuous improvement projects.
What We're Looking For
- Bachelor's degree in Chemistry or a related scientific discipline
- Experience within a pharmaceutical or regulated laboratory environment
- Hands-on experience with chromatographic techniques, particularly HPLC/UPLC and/or GC
- Experience working within cGMP and/or GLP environments is highly desirable
- Strong analytical, troubleshooting and problem-solving skills
- Excellent communication skills and the ability to work independently within a fast-paced QC laboratory.
Why Apply?
This is an excellent opportunity to join a growing organisation that supports the development and manufacture of life-changing therapies. You'll work within a collaborative analytical team, gain exposure to a broad range of QC activities, and have opportunities to expand your technical expertise and develop your career.
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