USA - Document Control Analyst

Job-ID29044922Reference26-22388Job Title – Quality Control Analyst Job Description – 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. 100% Onsite Primary Duties 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 % of Time Job duty and Description 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. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”