Quality Assurance Operations Associate (GMP)

Biotechnology company is hiring Quality Assurance Operations Associates to provide quality oversight for GMP documentation. This is a 4-month contract to start with the potential to extend.ResponsibilitiesProvide quality oversight of one or more portions of operations including, but not limited to:Review of GMP documentation from manufacturing, which can include but is not limited to logbooks, production batch records and electronic buffer & media batch records.Scanning and archiving executed production batch records.Ensure manufacturing adherence to company policies/procedures, regulatory licenses, industry standards, and GMP regulations.Working knowledge of United States and European regulatory requirements, guidelines, and recommendations a plus (additional jurisdictions a plus).Perform other duties and projects as assigned by management.QualificationsAssociate's degree or higher.2+ years of Biotechnology or Biopharmaceutical quality assurance experiencePay$32.22-$40.27/hrWhy Choose R&D Partners?As an employee, you have access to a comprehensive benefits package including:Medical insurance - PPO, HMO & HSADental & Vision insurance401k planEmployee Assistance ProgramLong-term disabilityWeekly payrollExpense reimbursementOnline timecard approvalR&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.R&D Partners is an equal-opportunity employer.