Hours: First Shift - Monday Though Friday (Can be flexible as long as working core hours between 9-3 (so can start at 7am, 8am, or 9am)
Requirements:
- Minimum two (2) years of relevant work experience
- Experience in Medical Device, Biopharmaceutical, or Pharmaceutical industry
- Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs)
- Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA
- Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols
- Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint)
Preferred:
- CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience
- Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC
- Ability to complete equipment and software qualification protocols
- Experience developing and setting long-term objectives
- Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility
- Experience, training, or certification in Lean, Six Sigma, or Process Excellence tools & methodologies
- Knowledge of EU/FDA guidance
Day to Day:
The QC CRS Analyst is responsible for conducting biochemical and testing of drug substance, final product release and characterization samples, and critical reagent qualifications of cell and gene therapy products, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 10 – 15 other Analysts within a functional Clinical Release and Stability (CRS) Laboratory and report to one of two QC CRS Supervisors.
Key Responsibilities:
- Conduct analytical biological testing (ELISAs, qPCR, Flow Cytometry, Cell-based assays, etc.) of clinical and commercial drug product/drug substance samples
- Perform peer reviews and approvals of laboratory data
- Use electronic systems (LIMS, MES, Empower, etc.) for execution and documentation of laboratory data
- Support of New Product Initiatives (NPI) in groups of 3-6 analysts
- Perform Instrument Calibration and/or Preventative Maintenance, as needed
- Update CRS-owned documents using the Electronic Document Management System (EDMS)
- Order/receive supplies and manage inventory
- Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities
- Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight
- Complete invalid assay and general laboratory investigation records
- Complete corrective and preventative actions (CAPA) as assigned
- Assist in the execution of internal audits
$35/hr to $45/hr.
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.