Sign-up for the Sterling-Hoffman Life Sciences Journal to get the latest industry news and job postings.		To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.  Job #02909 About our client Our client is an acute care specialty pharma company based in San Diego. They specialize in a technology that provides sustained-release delivery of medications for post-surgical pain. Our client has two marketed products that are used by professionals in the healthcare industry. The company has premier investors, an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. Position Location Process Equipment Engineer San Diego, Southern California Salary Highly competitive package, commensurate with experience Responsibilities 1) Provide process and equipment engineering capabilities and experience to the Technical Operations Project Team 2) Focus on the design and scale-up of new manufacturing equipment and monitoring procurement activities 3) Handle equipment fabrication, factory acceptance testing, site installation, site acceptance testing, start-up and validation 4) Work independently and use good judgment in carrying out functions 5) Provide process engineering design support services for the scale-up and commercialization of new products 6) Produce and review design drawings, including PFDs, UFDs and P&Ids 7) Supervise external engineering consultants 8) Provide process overview 9) Review drawings and documents produced by support groups 10) Provide key input into validation of process equipment and associated utilities, including generation of validation plans and protocols 11) Guide Manufacturing and Operations staff in the execution of validation protocols Requirements 1) BS in Engineering (Chemical Engineering preferred) 2) 2 – 5 years of experience in relevant equipment, clean utility and process systems 3) Minimum 2 years of experience in pharmaceutical/biotech industry 4) In-depth understanding of pharmaceutical manufacturing equipment and supporting utility systems (sanitary and sterile operations) 5) Knowledge of and experience in working in cGMPs environment 6) Knowledge of process control 7) Excellent applied problem-solving skills
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