I entered the industry of Biopharmaceutical processing eight years ago with a role in Contamination Control. Environmental Monitoring for Cleanrooms and Controlled Environments over the years has become my specialty. Currently Lead Production Chemist writing Standard Operating Procedures, creating facility cleaning schedules, developing quality assays, assisting process validation, and other technical documents along with manufacture drugs and medical devices. I work independently or in a team-based environment and I understand how an optimistic view encourages positive results. I appreciate the opportunities I've had and look forward to more opportunities in this industry, manufacturing lifesaving drugs and medical devices.

Highlights:

• Manufacturing
• Compliance
• ISO
• Clean Room
• Drafting
• Medical
• Medical Devices
• Monitoring
• Pharmaceutical
• Quality