Analytical Methods Specialist – QC & Validation
US Pharma Lab
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Benefits offered by this job
Job summary
US Pharma Lab is seeking an Analytical Technical Services Specialist to support QC analytics. The role combines hands-on lab work with independent technical responsibility for method development, validation, transfer, and troubleshooting of HPLC/UPLC, GC, FTIR/IR, UV-Vis, and dissolution analyses.
You will mentor QC chemists and collaborate with QA, R&D, and manufacturing, ensuring cGMP compliance, data integrity, and robust method documentation in a fast-paced nutraceutical/CDMO environment.
Qualifications
- Master's degree in Analytical Chemistry or related field.
- 5–7 years of experience independently managing analytical method projects.
- Experience in GMP/nutraceutical/pharma environments.
- Strong troubleshooting, data integrity, and documentation skills.
- Ability to lead investigations and CAPA.
Responsibilities
- Develop, verify, validate, transfer and optimize analytical methods.
- Serve as SME for methods and instrumentation.
- Perform complex analytical testing of materials and products.
- Review chromatograms and data integrity across reports.
- Lead investigations of OOS/OOT and deviations.
- Support CAPA and regulatory audits.
Skills
Education
Tools
Job description
US Pharma Lab is seeking an Analytical Technical Services Specialist to support QC analytics. The role combines hands-on lab work with independent technical responsibility for method development, validation, transfer, and troubleshooting of HPLC/UPLC, GC, FTIR/IR, UV-Vis, and dissolution analyses.
You will mentor QC chemists and collaborate with QA, R&D, and manufacturing, ensuring cGMP compliance, data integrity, and robust method documentation in a fast-paced nutraceutical/CDMO environment.
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