Sr. Process/Validation Engineer

The 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.  WORKING AT GENEZEN 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 SUMMARY The Sr. Process /Validation Engineer plays a key role supporting operations at Genezen’s gene therapy facility and will provide operational support to all groups including MFG, F AC , QC, SC, MSAT and PD. The incumbent will provide a variety of support services including equipment performance evaluation, troubleshooting, procedure development, process and equipment monitoring, validation / qualification, CI’s and leadership of medium to large projects .     ESSENTIAL JOB FUNCTIONS   Prepare, schedule, coordinate and monitor their assigned engineering projects   Manage projects associated with workflow optimization, mistake-proofing, and continuous improvement.   Supports change management processes to achieve desired business outcomes in a complex business environment.   Monitor compliance to all applicable FDA and EU practices, QA/QC policies, performance standards and specifications.   Interact daily with internal team members and external third parties to interpret their needs and requirements and represent them in the field.   Perform overall quality control of their work (budget, schedule, plans, personnel performance) and report regularly on project and maintenance/calibration status.   Cooperate and communicate effectively with team members, other project participants, and upper management to assist with technical support.   Be seen as technical engineering expert and be responsible for daily operations team huddle and daily site standup meeting providing updates on equipment, qualification status, documentation, and any CAPA’s or deviations.    Troubleshoot equipment and systems issues and develop solutions.   Ensure internal and external team members/contractors maintain the highest quality standards.   Identifying deficiencies in MEP processes and developing improvements.   Developing, initiating, and managing all phases of projects, maintenance/calibration.   Preparing documentation of critical analysis and providing suggestions for correcting errors across projects and maintenance/calibration.   SPECIAL WORK REQUIREMENTS Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION/CERTIFCATIONS/LICENSES BS/BA degree in Engineering, Science, Technical or related field   Essential   Pharmaceutical, Biomedical, or Medical Device experience   Essential   ON-THE-JOB EXPERIENCE 5 + years of engineering/project management experience   Essential Proven working experience as an Engineer, Project Manager with experience in CQV, master planning. CAPEX/OPEX, change control, and continuous improvements/optimization Essential Adherence to all local, state, and governmental safety standards Essential Excellent knowledge of design and visualization software such as AutoCAD Essential Familiarity with rules, regulations, best practices, and performance standards Essential SKILLS/ABILITIES Advanced MS Office skills Essential Project management and supervision skills Essential Decision making ability and leadership skills Essential Time management and organization skills Essential Ability to work with multiple discipline projects Essential Work Environment Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock Occasionally exposed to extremely loud noise levels Spending time on the floor during activity execution (maintenance, construction, commissioning, and qualification) is required Movement Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms  Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up to 10 pounds Occasionally lift and/or move up to 25 pounds Vision Frequently utilize close vision and the ability to adjust focus Communication Frequently required to communicate by talking, hearing, using telephone and e-mail GENEZEN'S CURES VALUE-BASED COMPETENCIES C ommitted to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. U rgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. R esilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success.  E xecute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. S olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S