Quality Intern

This internship is funded through a grant program with specific eligibility requirements. In accordance with the grant terms, applicants must be currently enrolled students at Southern New Hampshire University. We encourage all eligible students to apply.OverviewThe Advanced Regenerative Manufacturing Institute (ARMI) is a member-based, non-profit organization whose mission is to advance the bioeconomy of the United States. As part of its technical efforts, ARMI is applying advanced automation and analytical techniques to develop scalable, consistent, and cost-effective manufacturing processes for cells, tissues, and organs.The Impact That You Will MakeQuality Interns are instrumental to supporting PD-through-GMP operations. Taking a phase-appropriate approach, Quality Interns at ARMI help to maintain the facility, materials, and processes within a state of continuous control.The Quality Intern supports both Quality Assurance and Quality Control teams, with a primary focus on documentation. This is an excellent opportunity for a student to make an impact while learning about the cutting-edge fields of tissue engineering and automation.Your RoleSupport electronic and paper-based Quality System documentation management efforts, including scanning, filing, and organization of subsystems.Review data and executed forms generated across the manufacturing facility and QC lab for compliance with ALCOA++ principles.Support internal Quality auditing operations. Assist with QC microbiology activities such as environmental monitoring, media incubation, colony counting, and the identification of microbial recoveries.Support routine lab cleaning and material inventory.Assist with the creation and revision of SOPs, test methods, and data forms.Document all operations according to GDP.Your Skills And ExperiencesExceptional interpersonal, written and verbal communication skillsExperience working in a fast-paced, dynamic, collaborative team environmentHigh energy, commitment, initiative, and perseveranceProgress toward an Associate's or Bachelor's degree in a biological science discipline.Familiarity with GDP, GLP, and GMP principlesExperience with electronic Quality Management Systems Knowledge of FDA regulations, especially 21 CFR Part 210, 211, 610Aseptic gowning experience within a controlled cleanroom environmentStrong verbal and written technical communication skills Competency with MS Office suite, especially MS Word and ExcelCollaborative attitude, sense of curiosity, and eagerness to manifest positive changeHours Expected: 30 - 39 per weekBy applying, I understand that any offer of employment is contingent upon the successful completion of a background check, in accordance with applicable laws.