Associate Director/Director, Quality Control

About the role

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 Responsible for driving all aspects of the Analytical and Microbiological Quality Control (QC) laboratories at Genezen. This individual provides leadership, scientific and technical expertise for all QC activities, as well as support to Analytical Development for all method qualification/validation activities. This person is also the facility aseptic subject matter expert, including responsibilities for the environmental monitoring program. The ideal candidate must have in-depth knowledge and experience in a cGMP/ GLP testing lab. ESSENTIAL JOB FUNCTIONS Ensure timely in-process and release testing of early clinical grade biopharmaceuticals Maintain familiarity with current analytical and bioassay methods used for characterizing viral vectors (Assays include genome titer by Flow, ELISA, qPCR, ddPCR, genome integrity assay, empty/full particle ratio assay, and cell-based assays) Monitor, maintain and continuously improve the environmental monitoring program, including conducting Environmental Monitoring Performance Qualifications as needed Develop, implement and maintain EM trending program and metrics, including Annual Reports and evaluation of alert levels Develop, implement and maintain an in-house isolates program Responsible for Disinfectant Efficacy Program Responsible for the Analytical laboratory equipment systems and software (e.g., ddPCR, Flow, etc.) including purchase, calibration, IOPQ activities, etc. to meet the compliance (data integrity) requirements and project timelines. Support the Analytical Development team in qualification/validation of analytical methods to support the cGMP manufacturing of viral vectors Support the tech transfer of bioassays from clients to cGMP QC testing lab Represent QC Analytical and Microbiological in client meetings and programs Establish and maintain the stability program Oversee LIMS development, implementation, operation, troubleshooting and maintenance Responsible for all laboratory logistics activities including, but not limited to sample management, test/release schedule, cycle time matrix, capacity management, etc. Manage outside contract laboratory relationships, including method qualification/validations, investigations, audits, cost and invoices to meet project timelines and business requirements Support OOSs/OOTs and other lab investigations, deviations, CAPAs, change controls, audits, and training Analyze regulatory authorities' programs, guidance documents, and activities in areas relevant to testing of cell and gene products Develop, implement and present metrics for monitoring of lab operations and stability program Participation in client audits and regulatory inspections as SME and development of responses to observations Responsible for hiring and development of team members, conduct performance review and disciplinary actions. Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the QC functional area KNOWLEDGE, SKILLS, AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BS in a scientific/technical discipline Essential MS in a scientific/technical discipline Preferred ON-THE-JOB EXPERIENCE 7+ years of experience in a QC leadership position within the biological industry Essential Proven technical leadership and experience in bioanalytical methods (method development, validation and transfer). Methods include but not limited to: ELISA, PCR, qPCR, ddPCR, cell-based assays, and flow cytometry-based assays. Essential Familiarity with viral vector release assays Preferred Proven lab operations management experience Preferred 3+ years of cGXP experience Preferred SKILLS / ABILITIES Ability to maintain multiple projects and timelines Essential Strong people leadership skills Essential PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: 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

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