Quality Assurance Associate

Job DescriptionJob DescriptionAptask Global Workforce (AGW) is seeking a Quality Assurance Associate for an Onsite position with a Global Biotechnology Company located in West Greenwich, RI. This is a contract opportunity.In this vital role, you will be responsible for Plant Quality Assurance (PQA) 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.Please note: This is a 100% onsite position that works a rotating shift schedule. Week 1: Monday, Tuesday, Friday, Saturday. Week 2: Sunday, Wednesday, Thursday. Shifts are approximately 12 hours per day, from 6:45 AM to 7:00 PM.Responsibilities:Provide Quality oversight for Manufacturing operations to ensure that products are manufactured, tested, stored, and distributed according to current applicable regulationsEnsure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulationsPerform review and approval of cGMP processes, procedures, documents and records, including logbooks, batch records, attachments, and work ordersEnsure that deviations from established procedures are documented per proceduresEnsure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirementsAlert management of quality, compliance, supply and safety risksComplete required assigned training to permit execution of required tasksResponsible for being in clean room space for majority of time on shift which includes gowningCommunicate and collaborate with the PQA shift to ensure required tasks are completedRequirements:High school diploma/GED with 4+ years of work experience, OR Associate degree with 2+ years of work experience, OR Bachelor's degree with 6+ months of work experience, OR a Master's degreeExperience working in a cGMP environmentIndependent but able to work within a team structureProficient in Microsoft Office (Outlook, Word, Excel, PowerPoint, MS Teams)Knowledge of Good Documentation Practices and data integrity requirementsExcellent written and verbal communication skillsExperience collaborating within and across functional areasAbility to prioritize and navigate ambiguity with minimal oversight in a fast-paced environmentDesired skills:Bachelor's degree and 2 years of Quality/Manufacturing work experienceExperience with decision makingExperience with analytical testing and/or general compendia testingExperience working with batch records and other GMP documentationPay range: up to $28.85 per hourOnly candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.If you have the described qualifications and are interested in this exciting opportunity, apply today!Aptask Global Workforce (AGW)ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.Benefits of working with ApTask Global Workforce include:MedicalDentalVisionSick Pay (for applicable states/municipalities)Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.