Quality Control / Documentation Analyst

• Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as 079 activities are completed by the biochem team.
• This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing.
• In this role, the primary responsibility for the individual in this position is to assist in instrument/method projects with some supervision. The projects may require attending meetings based on the specific project, document writing/revising to ensure compliance with regulations and quality control practices.
• The person in this role may also be asked to revise documents to assist in the daily operations of the team.

Responsibilities:

• 75% Executing experiments and procedures as detailed by lab manager and staff.
• 25% Writing /revising documents procedures and validation documentation.

Education and Experience Requirements:

• Essential: Minimum Bachelor's degree in Chemistry/Biology/Biochemistry.
• Desired: Experience in a laboratory environment is preferred.
• Experience with Matlab or other chemometric software.