2nd shift Quality Control Operations Analyst -Sun-Wed (Contract) 999

QC Operations AnalystWithin our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/biopharmaceutical company.As a QC Operations Analyst, you will join the Cell and Gene Therapy Department to support QC operations in a fast-paced GMP environment. The ideal candidate will have GMP lab experience and excellent organization skills. The candidate will need to be flexible to working at Boston/Cambridge depending on need.Essential Functions:Work cross functionally with internal (facility, validation, metrology) and external (CTL, instrument vendors) teams to minimize day to day lab operations interruptionsIdentifying and creating processes that will ensure success within the QC labSample, reagent and chemical lifecycle managementEstablish, write, and update Standard Operating Procedures (SOPs) in compliance with GMP guidelines as needed in support of quality control operationsSets up and maintains instrumentation by working with the cross functional team (QC, QA, facility and vendors)Maintain QC equipment and perform regular performance verification/calibration as specified by equipment SOPCommunicates project status to project leader.Performs work assignments accurately, and in a timely and safe manner.Shift work applies - 2 roles:Candidate will train M-F then convert to one of the below shifts. Flexible during manufacturing runs - if working later, will have a later start time.Sun – Wed12:30 PM – 11:00 PM3:30 PM – 2:00 AM (manufacturing run) at least 2x a monthQualificationsEducation and Experience:Bachelor's degree in Chemical Engineering, Scientific Field, or equivalent and relevant formal academic / vocational qualificationPrevious GMP lab experience that provides the knowledge, skills, and abilities to perform the job is preferred (0-2 years industry experience)In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills and Abilities:GMP experience preferredAbility to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument useProficient in Microsoft Excel and Word (LIMS is a plus)Proven problem solving and troubleshooting abilitiesGood written and oral communication skillsTime management and project management skillsAbility to work in a collaborative work environment with a teamAble to lift and move objects up to 25 pounds.Pay Range$40-$43/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.