job summary: This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.The ideal candidate enjoys tackling challenges and excels at time management with attention to detail. location: West Greenwich, Rhode Island job type: Contract salary: $29.00 - 33.56 per hour work hours: 9 to 5 education: High School responsibilities: Performing analytical testing including time sensitive samples from Manufacturing (Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC/ Conductivity), Centralized Raw Material testing (compendial testing & microbiology), Environmental Monitoring and Critical Utilities, Sample Receipt and Aliquot.Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with safety guidelines, cGMP (Good Manufacturing Practices) practices and other applicable regulationsGenerates complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooksOperates laboratory equipment and instrumentationPerforms review and approval of assays, documents and recordsSupports troubleshooting and problem solvingAlerts management of quality, compliance, supply and safety risksSupports TRAs and deviations, as applicableCompletes required assigned training to permit execution of required tasksPerforms additional duties as specified by management What we are looking for: Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.Demonstrated ability to work independently and deliver right first time resultsExcellent communication skills (written and verbal)Must have focus on data integrityQualified to work in the U.S. without employer sponsorshipCommitment of a 40-hour work week (4 x 10hr shifts) in West Greenwich, RI qualifications: Experience: Bachelors degree OR Associate's degree and 1-2 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 3 years of Quality or Analytical Laboratory experience Preferred Qualifications 1-3 years of experience in GMP analytical laboratoryExperience executing analytical /biological testing per Methods and/or CompendiaExperience with QC analytical systems and/or Quality systemsSelf-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervisionStrong communication skills (both written and verbal)Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.Understanding of biopharmaceuticals process and related unit operationsStrong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracyIndependent, self-motivated, organized, able to multi-task in time-sensitive environments.Demonstrated experience in investigations and QC processes #LI-AO1 skills: High Pressure Liquid Chromatography (HPLC), Liquid Chromatography (LC), Good Manufacturing Practices (GMP), Quality Control (QC), Quality Control Testing Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.