Nico DeVerter

• Utilized TrackWise to initiate and level deviations discovered during manufacturing processes
• Assisted during investigations to initiate CAPAs, collect data, and perform effectiveness checks
• Recorded findings of AQL (Acceptable Quality Limits) using CGMP documentation
• Analyzed quality and performance data to support intersectional department operational decision-making.
• Provided regular updates to team leadership on quality metrics by communicating consistency problems or production deficiencies.
• Defined and implemented quality initiatives to reduce risk and promote safety.
• Developed training materials, SOPs, and work instructions to supplement new team member onboarding and maintain excellence.
• Display patient first mentality in every action

• Oversaw CGMP processes in Secondary Manufacturing
• Assigning daily roles to operators
• Reconciling manufacturing batch records to verify documentation and quantity is correct
• Displaying a patient first mentality
• Collaborated with other leaders to direct workflow and support operations.
• Proven ability to learn quickly and adapt to new situations.
• Excellent communication skills, both verbal and written.
• Demonstrated respect, friendliness and willingness to help wherever needed.
• Planned, organized and monitored resources to deliver efficient use of labor, equipment and materials.
• Skilled at working independently and collaboratively in a team environment.

• Maintained complete documentation and records of all purchasing activities.
• Accepted and processed supply requests from staff, and placed orders per procedures.
• Maintained consistent email communication with stores and suppliers to confirm and track orders and verify price revisions on purchase orders.
• Communicated with vendors regarding inventory needs and negotiated prices to maintain profit margins.
• Identified and resolved supply chain issues to mitigate delays and production disruptions.
• Based production goals based on incoming sales orders

• Monitored team performance and provided constructive feedback to increase productivity and maintain quality standards.
• Met personal daily quotas while documenting process on CGMP documents
• Worked with team to meet manufacturing goals to supply patients with necessary medical devices
• Assisted with FDA audits by meeting with auditors and preparing team with company supplied CGMP documents

12 credit hours towards Business Administration And Management- Currently pursuing degree