Experience

Celltex Therapeutics Corporation

• United States
• Biotechnology Research
• 1 - 100 Employee

• QA Associate

  • Apr 2023 - Present

  - Issuance and review of Manufacturing Batch Records - Issuance of Deviation/Non-Conformance and CAPA numbers - Organize and file current documents per the company's filing process - Recieve, track and file-controlled documents, such as LUMAC logs, batch records, Quality Control testing logs, training records, etc. - Recieve and manage incoming materials - Assist team in scanning, organizing, and indexing critical documentation - Be proactive in informing the team members of… Show more - Issuance and review of Manufacturing Batch Records - Issuance of Deviation/Non-Conformance and CAPA numbers - Organize and file current documents per the company's filing process - Recieve, track and file-controlled documents, such as LUMAC logs, batch records, Quality Control testing logs, training records, etc. - Recieve and manage incoming materials - Assist team in scanning, organizing, and indexing critical documentation - Be proactive in informing the team members of documents in jeopardy of being late - Support Quality Team members with other duties, such as the audit program, training program, outgoing and batch release processes Show less - Issuance and review of Manufacturing Batch Records - Issuance of Deviation/Non-Conformance and CAPA numbers - Organize and file current documents per the company's filing process - Recieve, track and file-controlled documents, such as LUMAC logs, batch records, Quality Control testing logs, training records, etc. - Recieve and manage incoming materials - Assist team in scanning, organizing, and indexing critical documentation - Be proactive in informing the team members of… Show more - Issuance and review of Manufacturing Batch Records - Issuance of Deviation/Non-Conformance and CAPA numbers - Organize and file current documents per the company's filing process - Recieve, track and file-controlled documents, such as LUMAC logs, batch records, Quality Control testing logs, training records, etc. - Recieve and manage incoming materials - Assist team in scanning, organizing, and indexing critical documentation - Be proactive in informing the team members of documents in jeopardy of being late - Support Quality Team members with other duties, such as the audit program, training program, outgoing and batch release processes Show less



Avance Biosciences, Inc.

• United States
• Biotechnology
• 1 - 100 Employee

• GMP Quality Specialist

  • Dec 2021 - Feb 2023

• GMP Quality Assistant

  • Jun 2021 - Dec 2021