QC Analyst II/III - Analytical

Genezen•Lexington, MA

3d•$80,000 - $100,000•Onsite

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 Analyst II/III will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs) in a GMP laboratory. This position is based at Genezen’s state-of-the-art facility in Lexington, MA. This role supports the daily and occasional 2nd shift or weekend operations within the Quality Control group via execution of analytical testing and Quality Systems. This includes but is not limited to in-process, release, and stability testing. Execution of quality systems entails deviations, corrective and preventive actions (CAPAs), investigations, Out of Specifications (OOS), and change controls. These activities are all performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures.

Requirements

BA or BS in Chemistry/Biochemistry or other related science
Minimum 2-5+ years (Analyst II) and 5–8+ (Analyst III) of laboratory base experience within QC testing capacity, preferably in cGMP environment.
High proficiency in HPLC methods and analysis, as well as other analytical methods.
Follow procedures trained on and complete documentation applying cGMP/GDP/ALCOA+.
Thorough understanding of industry testing requirements/standards
Computer literacy (MS Word, Excel, and LIMS)
Good/effective communication, organizational, and critical thinking skills with the ability to work well with others and independently
Identify gaps and propose solutions.

Responsibilities

Perform routine/non-routine testing and review of in-process, DS and DP release and stability samples in accordance with Standard Operating Procedures (q-PCR, HPLC (SEC, IEX, rpHPLC), ELISA, RI, HIAC, DLS, Osmolality, Western Blot, CE-SDS, etc.)
Performs peer review as SME of assay data with minimal errors.
Able to work effectively in internal/cross-functional teams as an active member.
Train and execute assays cross-functionally to support deadlines for release.
Participate in equipment validation, method transfer/qualification/validation, critical reagent qualification and special protocol execution as required.
Responsible for protocol and report generation/revision/review, as required.
Strong understanding of regulations, able to apply to any situation, and identify deficiencies w/ some guidance.
Establish, revise, review and maintain standard operating procedures.
Responsible for Quality Systems related to QC Operations such as identifying a deviation to procedure, perform investigation, Change Controls, CAPAs, OOSs, OOTs.
Promptly and proactively communicates gaps to key stakeholders and recommends solution w/minimal guidance.
Responsible for protocol and report generation/revision/review, as required.
Strong understanding of regulations, able to apply to any situation, and identify deficiencies w/ some guidance.
Promptly and proactively communicates gaps to key stakeholders and recommends solution w/minimal guidance.
Supports internal and external audits as required