Chemical Analyst - ReElement Technologies - Noblesville
(2026-02 - 2026-07)
- Performed compliance-focused testing to support safe laboratory operations.
- Trained team members on procedures, equipment use, and good practice standards.
- Coordinated testing activities while supporting GMP and GLP requirements.
- Identified process issues and supported corrective actions to improve safe operations.
Quality Control Chemist - Ompi Stevanato Group - Indianapolis
(2024-03 - 2026-02)
- Trained production staff and lab technicians on equipment use and lab procedures.
- Supported safe operations by troubleshooting equipment and maintaining testing systems.
- Wrote deviations and risk assessments to strengthen quality and compliance practices.
- Completed chemical testing and method validation in a regulated manufacturing environment.
Analytical Chemist - Oxford Global Resources
(2022-05 - 2024-03)
- Updated SOPs and training materials to support compliance and employee understanding.
- Reviewed controlled documents and validated data for regulatory accuracy.
- Maintained document control practices that supported quality and safety standards.
- Helped strengthen training content through process review and documentation updates.
GMP/QC Document Reviewer/SOP Writing & Revision Consultant - Oxford Global Resources
(2020-09 - 2022-05)
- Revised SOPs and guidance documents to support compliance in regulated environments.
- Implemented CAPA and deviation reporting processes to address quality issues.
- Created training outlines and process documentation for manufacturing teams.
- Reviewed data and documentation using GMP guidelines to support audit readiness.
Microbiology Support Specialist - Quest Diagnostic (formerly, Mid America Clinical Labs) - Indianapolis
(2018-05 - 2020-09)
- Led and trained a 12-person team on specimen processing procedures and safety rules.
- Monitored compliance with testing procedures and corrected workflow issues when needed.
- Investigated missing specimen issues and improved reporting processes to save time.
- Communicated with hospital staff to support accurate handling and follow-up on specimens.
QC Protein Chemistry Research Associate III - Covance - Greenfield
(2015-10 - 2018-05)
- Performed testing and calibration activities in a GMP-regulated laboratory setting.
- Reviewed protocols, data, and reports to support compliance with regulatory standards.
- Troubleshot assay issues and supported corrective action in laboratory operations.
- Helped ensure procedures met quality and safety expectations during testing work.
Analytical Chemist - NicePak PDI - Mooresville
(2010-08 - 2015-10)
- Conducted chemical testing while following GMP and GLP procedures.
- Recorded results accurately in laboratory systems and required documentation.
- Supported investigations and non-routine testing in a regulated environment.
- Presented lab findings and supported method transfer activities with the team.
Research Associate - Eli Lilly and Company - Indianapolis
(2001-09 - 2010-08)
- Followed GMP procedures for documenting and reporting validation test results.
- Troubleshot automated instruments and supported reliable operation of lab equipment.
- Performed analytical testing and calibration activities in a research environment.
- Monitored high-volume sample workflows while maintaining accurate records and controls.
