Assist in day-to-day QA Operations activities to ensure compliance with GMP and regulatory requirements. Support Quality disposition process by ensuring that all required documents are accurately and properly completed and compiled against approved procedures and specifications, including all related deviations. Support internal manufacturing processes through shop floor monitoring and documentation review. Participate in external manufacturing oversight activities, including review of batch records and quality documentation. Aid in incoming material release by verifying documentation and performing quality checks. Contribute to continuous improvement initiatives within QA Operations. Maintain accurate records and ensure timely completion of assigned tasks. Assist in drafting Standard Operating Procedures (SOPs), batch records, technical documents, and other document types utilized at the site. Contribute to continuous improvement initiatives by identifying opportunities to enhance process efficiency, reduce costs, or improve product quality. Maintain accurate and detailed documentation for all activities in compliance with regulatory standards. This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities Ability to climb ladders and lift up to 50 lbs. Eagerness to learn and adapt in a dynamic, regulated environment Strong organizational skills and ability to manage multiple tasks Commitment to maintaining high standards of safety, quality, and compliance. Strong analytical and problem-solving skills with attention to detail Proficiency in Microsoft Office Ability to work independently and collaboratively in a team-oriented environment Excellent written and verbal communication skills Ability to climb ladders and lift up to 50 lbs. Current enrollment in a Bachelor's or Master's degree program in engineering, science, or a related field. Basic understanding of pharmaceutical manufacturing processes, validation principles and regulatory requirements is preferred Prior internship or coursework in pharmaceutical manufacturing, process engineering, or quality assurance is desirable but not required All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment. Please note that immigration or visa sponsorship is not available for this position