Job title: Document Coordinator for Biologics Process Validation
Company: R&D Partners
Job description: R&D Partners is seeking to hire a Document Coordinator for Biologics Process Validation in Foster City, CA.Your main responsibilities as a Document Coordinator for Biologics Process Validation:Create, revise, and implement procedures, best practices, and business processes for the Biologics Process Validation programAct as a Project Manager to track and monitor Process Validation progress and deliverablesCoordinate Process Validation documentation: Prepare, edit, proofread, coordinate and adjudicate reviewer comments with author and subject matter expertsPerform Data Verification of completed Process Validation studies and reportsCreate study templates to drive alignmentWhat we are looking for in a Document Coordinator for Biologics Process Validation:Bachelor’s degree in life sciences or related fieldMinimum of four years experience in biotechnology, process validation, Quality, or a related areaMust have understanding and application of GMP principles, concepts, and practicesKnowledge of biochemical manufacturing process and terminologyKnowledge and experience in process validation in highly regulated manufacturing environmentsWhy 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 approvalPay Scale:$82,534 $103,168 (Dependent on Experience)R&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.
Expected salary: $82534 – 103168 per year
Location: California
Job date: Thu, 29 Aug 2024 22:09:12 GMT
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