Director, Quality Control
About The Position
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.
Requirements
- BS in a scientific/technical discipline
- 7+ years of experience in a QC leadership position within the biological industry
- 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.
- Ability to maintain multiple projects and timelines
- Strong people leadership skills
Nice To Haves
- MS in a scientific/technical discipline
- Familiarity with viral vector release assays
- Proven lab operations management experience
- 3+ years of cGXP experience
Responsibilities
- 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
Benefits
- Paid vacation days, amount based on tenure
- Paid sick time
- 10 observed holidays + 2 floating holiday + 1 volunteer day
- 401(k) plan with company match up to 6% of salary, vested immediately
- Share Appreciation Rights
- Choice of several healthcare plans
- FSA and HSA programs
- Dental & vision care
- Employer-paid basic term life/personal accident insurance
- Voluntary disability, universal life/personal accident insurance
- Accidental Death & Dismemberment (AD&D) Insurance
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What This Job Offers
Job Type
Full-time
Career Level
Director
