Fermentation Engineer at cGMP Consulting

About UsAt cGMP Consulting we specialize in providing expert validation qualification and compliance services to the life sciences industry. Our team works with clients to ensure their facilities equipment and processes meet regulatory standards enabling the safe and efficient production of pharmaceuticals.cGMP Consulting is based in Lake Forest IL. Our main client locations are Melrose Park IL North Chicago IL Waukegan IL and Pleasant Prairie WI.Job SummaryThis position is responsible for providing technical support to the Engineering teams for managing vendors commissioning testing and design review. The individual must have the ability to write reports clearly concisely and accurately. A basic understanding of current Good Manufacturing Practices (cGMP) is also required to perform these duties. Knowledge of controls is a plus.ResponsibilitiesPerforms specification procurement commissioning and operation of API processing equipment (reactors mix tanks centrifuges various types of filters dryers and drum filling equipment).Performs commissioning studies(utility equipment cleaning process computer and new products) which can alsoinclude writing Risk Assessments protocol preparation scheduling protocol execution and final report preparation.Programs and operates department analytical instruments (such as temperature/humidity dataloggers) to perform controlled temperature/humidity chamber qualifications (examples lyophilizers warehouses sterilizers incubators etc.).Represents Technical Services in teams assembled to specify install troubleshoot and maintain systems equipment and processes.Responsible for managing multiple deviation investigations simultaneously.Provides follow up and scheduling to qualification process is not impacted by outstanding deviations.Works with process experts and production personnel to fully understand and solve problemsProvides technical expertise and recommends improvements.Utilizes Word Excel Documentum and other electronic systems to complete tasks.Maintains compliance with company policies training requirements cGMPs and safety standards.Perform any other tasks/duties as assigned by Management.RequirementsMinimum 4-year degree in a Science or Engineering field of study1-3years of applicable cGMP manufacturingexperience writing standard operating procedures and protocols and/or reports. Familiar with regulatory (FDA) requirements.Ability to communicate clearly and concisely when conveying information summarizing facts asking questions etc.Compensation and BenefitsExpected pay range per year: $75000-$95000 USDExpected benefits include: Medical Dental Vision PTO 401KDisclaimerThe duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge skills or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer drug-free workplace and complies with ADA regulations as applicable. Required Experience:Junior IC Key Skills ASP.NET,Health Education,Fashion Designing,Fiber,Investigation Employment Type : Full-Time Experience: years Vacancy: 1 Monthly Salary Salary: 75000 - 95000