Job Description

Location: On-site in Upstate NY (Relocation from Canada welcome!)

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.Travel within USA as needed for the pr

ojects.
Perks & B

• enefits:Competitiv
• e salaryFull health, dental, vision, and retirement
• benefitsTuition reimbursement, PTO,

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