2nd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 843

Vertex Cell And Gene Therapy Quality ControlThe Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities under Good Manufacturing Practices (GMP) guidelines.The role is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation, testing, and reporting of in-process, release, and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.Shift - 2nd shift (12:30pm - 11:00pm est.) Wednesday - SaturdayTraining Monday-Thursday 11am-9:30pm (60-90 days)Candidate should have extensive experience working with flow cytometryKey Responsibilities:Typical test methods performed include, but are not limited to, flow cytometry, cell counting, cell culture, sterility (BACT), endotoxin (LAL), and Visual Inspection testing.Performs technical reviews of raw data.Records test results and maintain raw data and accurate laboratory records on paper and in electronic systems.Performs general lab and equipment maintenance duties.Performs other duties as assigned.Troubleshooting analytical methods and participating in Quality Events (Deviations, OOS).Knowledge and Skills:Performs tasks with strict adherence to cGMP and cGDP principles.Has an understanding of basic laboratory equipment and practices.Is proficient in the use of spreadsheets and word processing software.Is dependable and able to work well within a team.Is interested in learning new things. Open to change.Is optimistic and displays a positive attitude even during periods of adversity.Shows initiative; acts independently with management approval.Possesses a high attention to detail.Experience with electronic lab notebook (LIMS), and demonstrated ability to work with electronic instrument softwareRequirements:A minimum of a Bachelor's degree in related field of science is required (Biology, Biochemistry, etc).Sr. Associate: 2-4 years, Specialist: 4-6, Sr. Specialist 6-8 years of experience in the GMP pharmaceutical/biopharmaceutical industryDemonstrated laboratory experience in multiple methodologies listed abovePay RangeSr. Associate - $40-44/hrSpecialist - $44-$46/hrSr. Specialist - $50-$55/hrRequisition DisclaimerThis job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements Ver-Tex