QC Analytical Lab Technician

Purpose and Scope of the Position Bristol Myers Squibb is seeking a QC Analytical Lab Technician at the Cell Therapy Facility (CTF) in Devens, MA. The QC Lab Technician will support Quality Control bioanalytical testing for method validation, critical reagent qualification, in-process, release, and stability testing of clinical and commercial cell therapy drug product. The role requires the ability to interface with multiple groups, perform tasks independently, interpret results, and troubleshoot. The position is stationed in Devens, MA and reports to the Manager, QC Analytical for the Devens CTF. Top 3 to 5 Skills / Must Haves Pipetting technique Assay – Some level of analytical chemical bench testing Assay execution CGMP Knowledge 1 to 2 years industry experience Job Responsibilities Perform routine testing of in-process, final product, and stability samples. Use scientific principles to assist with analytical testing methods and the proper use of laboratory equipment. Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Review all data in accordance with applicable procedures and cGMP requirements. Anticipate and troubleshoot problems. Communicate effectively with management regarding task completion, roadblocks, and needs. Support document revision, project, CAPA, and investigation/deviation related tasks. Perform assigned tasks within a CAPA, deviation, or project. May lead projects and continuous improvement efforts. Perform other tasks as assigned. Provide shift coverage for QC and manufacturing operations on weekdays, weekends, holidays, and during adverse weather conditions. Qualifications and Education Requirements Bachelor?s degree required, preferably in Science. 2 years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment. Hands on experience with various bioanalytical techniques (cell based assays, flow cytometry, ELISA, qPCR) and scientific knowledge in the methods. Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. Strong technical writing skills. Strong problem-solving ability/mentality, technically adept and logical. Ability to represent the interests of the group on cross-functional teams. Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work. Strong ability to communicate effectively with peers, department management and cross-functional peers. Ability to work with management locally and globally. Working knowledge of LIMS. Work Location Devens, MA Shift A2 – Sun to Wed, 2:00 PM to 12:00 AM Starting Hourly Compensation $47.00 – $50.05 per hour (Contract assignment details may vary). Equal Opportunity Employer ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws. #J-18808-Ljbffr Bristol Myers Squibb