Ashley Dreesen Email & Phone Number

Indianapolis, Indiana, United States

• Oversees automation and routine work for the group. Aid in training and educating technicians on methods and analytical techniques.• Participate in method development and optimization for previous and newly requested methods. Transfer in methods from the pilot plant.• Participate in weekly, biweekly, and monthly meetings with stakeholders to ensure an efficient workflow. Lead the analytical group meeting.• Update and create method SOPs.• Present updates to stakeholders and a broader group of researchers.• Serve as Area Focal Safety Point and present monthly on safety topics.• Create and maintain a multi-generational plan for the analytical group.• Serve as a member of the social committee to engage and show appreciation to everyone in the department.• GC focal point.• Actively use CHROMEAcademy to increase analytical knowledge while creating training modules for the group.

Indianapolis, Indiana Area

• Serves as shift lead. Train new employees and educate on analytical knowledge. Building leadership skills by leading without authority.• Performing accurate and timely testing performing analytical testing of batch release and stability samples.• Perform second person verification.• Proficient in all analytical testing performed in lab. Demonstrate proper data documentation.• Apply technical knowledge to recognize complex problems/atypical results.• Maintains a clean and safe laboratory work environment. Performs other related duties as assigned.• Organize and conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. • Act as an investigator for laboratory investigations and identifying root cause.• Participate in different studies for reference standards, column equivalency, and method transfers.• Subject matter expert for maintaining notebook inventory for entire laboratory. Maintaining used column inventory. • Contributes towards a cohesive team environment.

Indianapolis, Indiana

• From April 2011 to January 2012 employed by Kelly Scientific.• From January 2012 to October 2015 employed by Lancaster Laboratories• From October 2015 to July 2016 employed by Lancaster Laboratories at Eli Lilly.• Proficient in method development of GC and HPLC analyses of various analytes in different matrices and troubleshooting instrumentation. Maintains a clean and safe laboratory work environment. Performs other related duties as assigned.• Organize and conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. • Principal Investigator on standard certifications of active ingredients, metabolites, impurities, and formulations, method validations of formulations, batch analyses , tox-lot characterizations, analytical standards, and physical chemical properties studies. • Perform mass spectral analysis for structure confirmation and unknown identification purposes, providing data interpretation in a GLP report as necessary. • Perform DSC purity analysis for standard certifications.• Document work and maintain study documentation and laboratory record, ensuring all documentation meets GLP standards.• Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems. • Contributes towards a cohesive team environment. • Instrumentation used: GC, HPLC, LCMS, GCMS, pH meter, Ezchrom, DSC.

Greenfield, Indiana

• Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.• Documents work and maintains study documentation and laboratory records.• Sets up, operates and performs routine and non-routine maintenance on general equipment.• Provides input and participates in project meetings, plans, monitors, and guides project work.• Performs QC review of data.• Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems.• Contributes towards a cohesive team environment.• Assists in setting and performing method development and validation of various analytes in a variety of matrices. • Maintains a clean and safe laboratory work environment. Performs other related duties as assigned.• Instrumentation used: Dissolution, HPLC, pH meter, Empower.

Indianapolis, Indiana

• Performing accurate and timely testing performing analytical testing of clinical trial drugs (both lot release and stability) in accordance with GMP and safety regulations.• Subject matter expert for all dissolution methods performed in lab• Ordering and organize all standards used in the laboratory.• Tests performed included dissolution, industrial hygiene development, potency, impurities, unit dosage unit, and physical appearance.• Performed dissolution co-qualifications of newly developed methods.• Apply technical knowledge to recognize complex problems/atypical results.• Demonstrate proper data documentation.• Instrumentation used: Dissolution, HPLC, UV-Vis, pH meter, disintegration, Empower.

Indianapolis, Indiana

pharmaceutical products in accordance with GMP and safety regulations.• Quality and compliance to establish standards and safety.• Tests performed included swab analysis, potency, related substances, basic id, dissolution, hardness, uniform dosage unit, and physical appearance.• Perform equipment requalification. Investigate deviations and perform root cause analysis.• Apply technical knowledge to recognize complex problems/atypical results.• Demonstrate proper data documentation.• Modify departmental worksheets and write departmental work instructions.• Log in of samples when deemed appropriate.• Instrumentation used: Dissolution, HPLC, UV-Vis, pH meter, TOC analysis, hardness testing, Empower.

Bachelor'S Of Science, Chemistry

Activities and Societies: Alpha Chi Sigma, Purdue Bowling Team, WISP, Science Olympiad

Education record