Process Engineer

Location: On-site in Upstate NY (Relocation from Canada welcome!) Do you have the skills to fill this role Read the complete details below, and make your application today. Please note: We are only considering W2 candidates at this time. Applications from third-party vendors or C2C arrangements will not be considered . ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Headquartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system project s. ADVENT's services include process engineering, automation engineering, project engineering, facility/system design, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing compani es.The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill s et. This is an outstanding opportunity to join our growing t eam ! Full-Time | O nsiteAbout the Role:We are seeking a detail-oriented and technically profic ient Process Engi neer who will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. Responsibi litiesWork with Upstream equ ipmentFermen tationProcess optimi zationProcess scale-up or scale-down s tudiesCommissioning and Qualifi cationProtocol generation and exe cutionData an alysisReport w ritingAutho r SOPsGreat communication skills (presenting, and wr iting)Protein expression/purifi cationGxP (GDP, GLP, or GMP a major asset) Minimum Requi rementsBachelor’s or master’s deg ree in Biochemistry, Biology, Mechanical Engineering, Chemical Engineering, Biochemical Engineering, or related dis c ipline.Required: 5 + years of experience in the biotech-pharmaceutical academic or industrial envir onment.Bioprocess experience pr eferredFill finish experience pr eferredBasic knowledge of upstream/downstream drug substance manufac turing.Basic knowledge of regulatory compliance inclusive of cGMP, OSHA, EPA, FDA regulations. Familiarity with ICH guidelines and EMA regulations is a plus.Basic technical writing with proficiency in Excel, PowerPoint, Visio, Word, Sharepoint, etc. in addition to experience working within shared work enviro nments.Demonstrated experience with manufacturing processes and equipment such as CIP systems, bioreactors, filtration skids, chromatography and lyophilization equ ipment.Basic knowledge of the Commissioning and Qualifi cation. xmvmafu Travel within USA as needed for the pr ojects. Perks & B enefits:Competitiv e salaryFull health, dental, vision, and retirement benefitsTuition reimbursement, PTO, and more