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Job description
Manufacturing Technician I/II/III (Contract)Indianapolis, INThe field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.Job SummaryResponsible for supporting projects from advanced laboratory techniques related to viral vector production and analytics to routine performance of upstream and downstream manufacturing operations including aseptic cell culture technique, preparing solutions and media, molecular biology techniques, chromatography, TFF and general cleanroom sanitization/area maintenance. The position requires working independently, but also under the supervision of experienced personnel.Essential Job FunctionsExecute hands on project work from process development through manufacturing related to viral vector production including upstream and downstream GMP manufacturing tasks under the guidelines of established procedures and batch recordsPerform hands on laboratory procedures related to viral vector production and characterizationPerform daily operations in the scale-up, production, harvest, clarification, purification, and fill/finish of retro, lenti, and AAV viral vectors.Execute production activities including cell thawing, cell passaging, bioreactor inoculation, clarification filtration, chromatography, tangential flow filtration, sterile filtration and filling of viral products following GMP guidance and according to applicable batch records.Maintain appropriate GDP documentation of processing activitiesPerform routine lab maintenance and maintenance of laboratory equipmentAssist in the development of general and technical SOPs and with the creation of client specific procedures and batch recordsMaintain manufacturing material supply, primarily ensuring manufacturing spaces are adequately stocked and preparedAssist in the maintenance of laboratory equipment and laboratory support operationsFollow detailed instructions with a high level of focus and attention to detailComplete documentation accurately and in a timely fashionMaintain up to date training statusUse, clean, and maintain lab and manufacturing equipmentAssist in troubleshooting of upstream and downstream manufacturing issuesCross train new staff members and fellow employees in designated processesComply with all established policies and SOPsPerform safety inspections and maintain a safe working environmentParticipate actively in continuous improvement activities and SOP revisions in coordination with management and Quality AssurancePerform area sanitization and collect/dispose of waste per established proceduresHelp collect process data for metrics/trendingUse and maintenance of cGMP equipmentSpecial Job RequirementsAdaptability required as work schedule may change based on business needsCriminal background check requiredOther duties as assignedKnowledge, Skills and ExperienceEDUCATION / CERTIFICATIONS / LICENSES - Essential/DesiredAssociate or BS degree in Biology, Biochemistry, Molecular Biology, or similar field - Strongly DesiredON-THE-JOB EXPERIENCE1-4 years of relevant cleanroom GMP industry experience in R&D, product development, or operations - EssentialUpstream Cell culture experience with mammalian or insect cell culture in adherent or suspension platforms. Experience with bioreactor inoculation and harvest - DesiredExperience with downstream purification techniques including Affinity Chromatography, Anion Exchange Chromatography, Ultracentrifugation, Nanofiltration, Tangential Flow Filtration, Sterile Filtration, and Fill/Finish. - DesiredAseptic operations in a Class 7 (Grade C) or higher cleanroom setting - DesiredSKILLS / ABILITIESExcellent computer, verbal, and written communication skills - EssentialAbility to work independently with minimal supervision as well as working effectively as part of a team - EssentialAble to adapt quickly to changing ideas, responsibilities, strategies, and other processes - EssentialWilling to work in an environment where individual initiative, collaboration, and accountability are valued - EssentialPhysical DemandsWhile performing the duties of this job, the employee is required to meet the following physical demands:Work EnvironmentFrequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowningRegularly required to work around large machinery and typical utilities seen in pharmaceutical facilitiesOccasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shockOccasionally exposed to extremely loud noise levelsMovementFrequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and armsOccasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawlLiftingFrequently lift and/or move up to 25 poundsOccasionally lift and/or move up to 50 poundsVisionFrequently utilize close vision and the ability to adjust focus CommunicationFrequently required to communicate by talking, hearing, using telephone and e-mailGenezen's Cures Value-Based CompetenciesCommitted to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.Urgency in Action for the Patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.Resilience & Grit in Operations We are committed to overcoming challenges, learning from failures, and persistently striving for success.Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals.Solutions Driven for Our Partners We are committed to being a proactive, collaborative, creative and open-minded partner.Genezen's BenefitsPaid vacation days, amount based on tenurePaid sick time10 observed holidays + 2 floating holiday + 1 volunteer day401(k) plan with company match up to 6% of salaryShare Appreciation RightsChoice of several healthcare plansFSA and HSA programsDental & vision careEmployer-paid basic term life/personal accident insuranceVoluntary disability, universal life/personal accident insuranceAccidental Death & Dismemberment (AD&D) InsuranceAdditional DetailsNothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.This position requires a criminal background check.Genezen is an Equal Opportunity Employer.Genezen participates in EVerify.Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.
Worksite address
indianapolis, IN, 46201, US
Who can apply
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