QC Analyst - Bioassay (Temporary, 2nd shift, Wed-Sat)

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 Analyst will be responsible for routine and non-routine QC testing within the Bioassay team within a GMP laboratory. This is a 2 nd shift, Wednesday-Saturday, fully on-site, position (1 – 11.30pm) based at Genezen’s new state-of-the-art facility in Lexington, MA. This role supports daily operations within the Quality Control group through execution of cell-based testing, routine lab support and working within Quality Systems. This includes but is not limited to in-process testing, lot release testing, and stability testing. Support outside of standard shift hours is required occasionally and the initial work period will be on Mon-Fri. All activities are executed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures. ESSENTIAL JOB FUNCTIONS Perform routine/non-routine cell-based testing and review of in-process, DS and DP release and stability samples in accordance with Standard Operating Procedures (q-PCR, ddPCR, cell culture, ELISA) Perform peer review as SME of assay data with minimal errors. Participate in equipment validation, method transfer/qualification/validation, critical reagent qualification and special protocol execution as required. Review/generate protocols and reports, as required. Establish, revise, review and maintain standard operating procedures. Promptly and proactively communicates gaps to leadership Work as an active member of internal/cross-functional teams Train other analysts, as required. SPECIAL JOB REQUIREMENTS Strong understanding of GxP regulations, ability to apply to any situation, and identify deficiencies w/ some guidance. Adaptability required as work schedule may change based on business needs. Criminal background check required (completion by staffing agency satisfies this requirement). Other duties as assigned. KNOWLEDGE, SKILLS AND EXPERIENCE EDUCATION / CERTIFICATIONS / LICENSES Essential/Desired BA/BS in Biochemistry/Cell Biology or other related science Essential ON-THE-JOB EXPERIENCE Minimum 2 years’ laboratory base experience within QC testing capacity, preferably in cGMP environment. Essential Thorough understanding of industry testing requirements/standards Essential SKILLS / ABILITIES Computer literacy (MS Word, Excel, and LIMS) Essential Good/effective communication and organizational skills with the ability to work well with others and independently. Essential PAY RATE: This position is being filled through a third-party staffing agency and is a temporary assignment. The anticipated hourly pay range for this position is $30 - $40 per hour, based on qualifications, skills, experience, and other job-related factors. PHYSICAL DEMANDS While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Regularly sit for long periods of time 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 Rarely lift and/or move up to 25 pounds Vision Frequently…