QC Senior/Principal Scientist, Analytical Method Validation

Genezen•Lexington, MA

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 The QC Senior/Principal Scientist for Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department within our CDMO facility. The individual in this role will work collaboratively with new and current clients, analytical development team, quality control, manufacturing and quality assurance. Lead transfer and validate next generation analytical procedures for the testing of viral vectors, cell banks and gene therapy products in support of Genezen’s services and commercial products in compliance with company policies and procedures and regulatory guidelines.

Requirements

Ph.D or MS in Molecular Biology/Biochemistry or other related Life Sciences
Minimum 8 years of analytical laboratory experience in GLP/cGMP environment ideally associated with analytical method validation and transfer.
Prior experience with analytical method validations, analytical data trending/statistical analysis
Understanding of QC instrument qualification is preferred.
Thorough understanding of industry testing requirements/standards
Preferred experience with performing cell based bioassays using mammalian cell-lines (such as HELA, HEK-293, Huh-7 etc.) along with QC instrument qualification is essential.
Thorough understanding of industry testing requirements/standards related to gene/cell therapy products.
Familiar with ICH, FDA and EMA guidance documents relevant to gene/cell therapy.
Working knowledge of quality systems requirements
Computer/software literacy (MS Word, Excel, JMP, Minitab, and LIMS etc.)
Ability to thrive in a quickly changing, CDMO environment where flexibility and teamwork is essential
Ability to work in a fast-paced, collaborative environment, working with minimal direction and able to manage workload based on changing priorities
Proven demonstration of technical writing skills such as protocol, reports, procedures etc.
Effective project management and presentation skills
Good/effective communication and organizational skills with the ability to work well with others and independently

Responsibilities

Ability to work in a fast-paced, collaborative environment, working with minimal direction and able to manage workload based on changing priorities.
Works independently and is responsible for optimization, qualification, transfer and validation of analytical methods associated with cGMP production.
SME for cell-based and analytical method protocols and reports related to QC Method transfer, qualification, feasibility and validation.
Perform statistical analyses of data generated during method validation studies, qualification and critical material qualification.
Responsible for monitoring analytical method performance, including assessment of analytical method system suitability requirements.
Present to cross-functional teams and effectively communicate critical analytical issues and solutions.
Coordinate with Critical Material Sr. Scientist to design and qualify critical materials required for cell based methods to support phase appropriate readiness
Support cGMP operations, including generation of documentation in support of change controls and corrective actions/preventative actions, deviations, out-of-specification (OOS) results, and other investigations or assay troubleshooting.
Subject matter expertise in product quality attribute methods relevant to gene therapeutic product (e.g. cell function characterization assays, HPLC, ddPCR / qPCR, ELISA, Potency Assay, plate-based assays, CE-SDS, SDS-PAGE and western blot) and/or viral vector manufacturing.
Familiar with FDA and EMA guidance documents relevant to gene therapy.
Working knowledge of quality systems requirements.
Demonstrated leadership skills and the ability to collaborate with and effectively influence others.
Interface with clients and Genezen cross-functional teams to define technical requirements and provide routine project updates.
Assure that laboratory procedures are current and facilitate updates as required
Provide coaching to QCTS scientists and develop and contribute to their technical development
Lead training of new analytical methods and support QC analysts on execution, data analysis and technical review of data generated in GMP lab.
Complete documentation in accordance with current Good Manufacturing Practices (cGMP).
Identify, lead, and/or support continuous improvements to current processes/procedures accordingly for increased compliance and efficiency
Support onboarding and qualification of new instruments in cGMP laboratory environment.
Adaptability required as work schedule may change based on business needs
Criminal background check required
Other duties as assigned