Pam Footman

Safety Specialist with experience improving workplace safety, delivering employee training, reviewing safety programs, and conducting inspections and audits. Brings a strong background in compliance, process improvement, and team training to help reduce injuries, strengthen safe work practices, and support a safer work environment.

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.

MBA - Business Administration - Purdue university (2019-01 - 2021-12)

Bachelor's degree - General Studies - Indiana University-Bloomington (2006-08 - 2010-05)

Associate in Science - Chemistry - Indiana Institute of Technology (1999-01 - 2001-01)