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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 Lead the establishment of methods in the Analytical Development (AD) and Quality Control lab from the bench. This individual will be accountable for development and validation of analytical and QC assays, equipment specification and selection and the direction of analytical method transfer from the analytical development lab to the QC lab while operating under cGMP standards. The person is expected to work collaboratively with the team to establish and implement best regulatory, laboratory practices and to lead the execution of complex experiments. The position requires expertise in potency and other cell based assays, ddPCR/qPCR, and ELISA. Considerable expertise with experimental design toward method qualification and validation per ICH guidelines in a phase appropriate manner. Considerable expertise with technical writing of protocols, SOPs, and technical reports. Experience with biophysical characterization methods including HPLC, LC-MS, CE-SDS etc. Direct line management experience is required. JOB RESPONSIBILITIES Experience with AAV assay development is critical Expert in method qualification/validation experimental design per ICH guidelines Experience with specification setting for complex biologics Expert in potency method development  Expert in ddPCR/qPCR from primer design and optimization to implementation Expert with ELISA assay development Experience in HPLC based methodology development and establishment including with the use of CAD and MALS detectors for use in the characterization of AAV vectors Maintain familiarity with other current analytical and bioassay methods, including Flow cytometry Maintain familiarity with current equipment used in Analytics lab Help management evaluate new technology and bring new platforms in-house Qualify/validate analytical methods to support cGMP testing Help facilitate tech transfer of analytical and bioassays from clients to AD lab and from AD lab to QC lab Supervise and train AD Associates and AD Technicians and work closely with other departments, assisting in project planning Support the establishment of electronic record keeping systems for site; e.g. LIMS or ELN Analyze regulatory authorities’ programs, guidance documents, and activities in areas relevant to testing of biological products Work as a team with process development, manufacturing, quality assurance and quality control departments as needed Advise site and quality management of potential and actual actions that could adversely affect the business, represent quality exposures, or represent opportunities to be pursued Execute research timelines to meet program and corporate objectives Deal with abstract and concrete variables in situations where only limited standardization exists Maintain high quality deliverables and open communication, creating a collaborative working environment Contribute to collaborative, creative and rigorous culture of scientific discovery Provide weekly reports to department head in 1:1 environment SPECIAL JOB REQUIREMENTS People training and leadership skills Ability to mainta