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.

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.

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.
• 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.

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.

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.

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.

Bachelor'S Of Science, Chemistry

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

Education record