Quality Assurance Senior Associate

HERE’S THE JOB DESCRIPTION: Title: Quality Assurance Senior Associate 13295 (2 openings) Pay Rate: up to $34.00/hr Location: West Greenwich, RI 02817 Length: 1 year contract possible extension This position works a rotating shift schedule, Week 1: Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday, Thursday, 12 hours per day 6:50 AM – 7:00 PM Job Summary: In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. Top Must Have Skills: cGMP experience Experience collaborating within and across functional areas and demonstrated customer service focus Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment Responsibilities: Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current applicable regulations. Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations. Performs review and approval of cGMP processes, procedures, documents and records. Ensure that deviations from established procedures are investigated and documented per procedures. Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements. Alert management of quality, compliance, supply and safety risks. Complete required assigned training to permit execution of required tasks Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls. Communicating and collaborating with the PQA shift to ensure required tasks are completed Day to Day Tasks: Quality Oversight (including Purposeful Prescence on the Floor) of bulk drug substance manufacturing operations GMP documentation review/approval (including EURs, electronic logbooks, RT reports, Work Orders, batch records, etc.) Interim and reject cage management Preferred Qualifications: Bachelor’s Degree and 2 years of Quality/Manufacturing experience Experience working in a cGMP environment Experience with decision making Experience with analytical testing and/or general compendia testing Experience working with batch records and other GMP documentation Knowledge of data integrity requirements Proficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams) Experience collaborating within and across functional areas and demonstrated customer service focus Excellent written and verbal communication skills Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment